Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

2 structures for Q9ULJ3

Entry ID Method Resolution Chain Position Source
1WJP NMR - A 713-806 PDB
AF-Q9ULJ3-F1 Predicted AlphaFoldDB

847 variants for Q9ULJ3

Variant ID(s) Position Change Description Diseaes Association Provenance
CA321461573
rs902602830
3 G>R No ClinGen
TOPMed
rs780281032
CA10038982
10 P>R No ClinGen
ExAC
TOPMed
gnomAD
rs781233991
CA10038979
13 A>T No ClinGen
ExAC
gnomAD
CA10038978
rs757094590
14 I>V No ClinGen
ExAC
gnomAD
rs1298401147
CA410357528
16 L>F No ClinGen
gnomAD
CA410357483
rs763805003
19 A>P No ClinGen
ExAC
TOPMed
gnomAD
CA10038976
rs763805003
19 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA321461541
rs867395146
19 A>V No ClinGen
Ensembl
CA410357435
rs1384665480
23 E>K No ClinGen
gnomAD
rs1161701273
CA410357429
23 E>V No ClinGen
gnomAD
COSM188359
rs752261617
CA10038974
24 R>H large_intestine [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
CA10038973
rs764705098
25 L>P No ClinGen
ExAC
CA410357363
rs1251438864
28 Q>R No ClinGen
gnomAD
rs773741167
CA10038971
35 I>T No ClinGen
ExAC
gnomAD
CA10038970
rs767864423
36 V>I No ClinGen
ExAC
gnomAD
CA410356053
rs1290256551
37 G>A No ClinGen
gnomAD
CA410356025
rs1243050363
38 D>E No ClinGen
gnomAD
rs889221890
CA321461480
42 R>* No ClinGen
Ensembl
CA10038967
rs768994052
42 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1050925549
CA321461469
44 H>R No ClinGen
Ensembl
rs775749104
CA410355864
47 V>F No ClinGen
ExAC
TOPMed
gnomAD
CA10038965
rs775749104
47 V>I No ClinGen
ExAC
TOPMed
gnomAD
rs770020930
CA10038964
49 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA410355762
rs1472463832
52 S>C No ClinGen
TOPMed
CA10038962
rs143202688
COSM255040
53 E>K urinary_tract [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
CA410355753
rs143202688
53 E>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1601638235
CA410355701
56 Q>E No ClinGen
Ensembl
CA10038959
rs532170692
56 Q>H No ClinGen
1000Genomes
ExAC
gnomAD
CA321461417
rs940891126
61 N>D No ClinGen
Ensembl
CA10038958
rs777416725
61 N>S No ClinGen
ExAC
gnomAD
CA410355596
rs758118890
65 E>D No ClinGen
ExAC
gnomAD
rs1234888993
CA410355584
66 S>L No ClinGen
gnomAD
rs752316696
CA10038956
67 Q>K No ClinGen
ExAC
gnomAD
rs778497406
CA10038955
68 T>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA10038954
rs754508790
69 V>G No ClinGen
ExAC
gnomAD
CA410355530
rs1237856044
72 L>F No ClinGen
gnomAD
CA321461389
rs909456636
77 P>S No ClinGen
gnomAD
CA321461378
rs746120628
82 N>S No ClinGen
Ensembl
rs1223831924
CA410355371
87 I>L No ClinGen
gnomAD
rs1281290342
CA410355342
89 S>C No ClinGen
gnomAD
TCGA novel 90 S>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10038948
rs763366410
91 S>F No ClinGen
ExAC
gnomAD
rs1402053339
CA410355287
94 V>A No ClinGen
TOPMed
CA410355295
rs1408484857
94 V>L No ClinGen
gnomAD
CA410355286
rs1205673919
95 E>K No ClinGen
TOPMed
gnomAD
TCGA novel 97 S>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410355261
rs1480307936
98 S>G No ClinGen
gnomAD
CA410355259
rs1427719378
98 S>N No ClinGen
TOPMed
gnomAD
CA410355235
rs1429682700
102 V>L No ClinGen
gnomAD
TCGA novel 111 I>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410355162
rs1213870432
112 S>F No ClinGen
TOPMed
rs1203998048
CA410355147
115 T>A No ClinGen
gnomAD
rs759691586
CA10038945
117 I>V No ClinGen
ExAC
gnomAD
rs377604420
CA10038943
118 V>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038942
rs377604420
118 V>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1322520228
CA410355121
119 S>C No ClinGen
TOPMed
gnomAD
rs199683392
CA321461246
120 K>E No ClinGen
Ensembl
CA410355101
rs777665201
122 P>L No ClinGen
ExAC
gnomAD
CA10038941
rs777665201
122 P>R No ClinGen
ExAC
gnomAD
rs755389573
CA321461229
125 P>A No ClinGen
TOPMed
gnomAD
rs747891800
CA10038939
125 P>L No ClinGen
ExAC
gnomAD
CA10038937
rs754562350
127 P>L No ClinGen
ExAC
gnomAD
CA10038936
rs113061522
128 T>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038935
rs779420714
128 T>M No ClinGen
ExAC
TOPMed
gnomAD
CA410355066
rs779420714
128 T>R No ClinGen
ExAC
TOPMed
gnomAD
rs1191736060
CA410355047
131 N>S No ClinGen
TOPMed
gnomAD
CA410355037
rs1380987609
132 R>S No ClinGen
TOPMed
TCGA novel 135 V>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410355019
rs1569106951
135 V>M No ClinGen
Ensembl
rs796812009 135 V>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA321461133
rs201747023
136 F>C No ClinGen
gnomAD
CA410355003
rs1244485020
137 V>A No ClinGen
gnomAD
rs370846299
CA10038933
138 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038932
rs147026959
139 D>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 139 D>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs970588623
CA321461105
140 D>G No ClinGen
TOPMed
gnomAD
rs1240920511
CA410354986
140 D>H No ClinGen
gnomAD
CA410354983
rs970588623
140 D>V No ClinGen
TOPMed
gnomAD
CA410354968
rs1250679193
142 N>S No ClinGen
gnomAD
CA10038928
rs149797502
143 S>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038927
rs149797502
143 S>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs759817211
CA10038926
145 Q>* No ClinGen
ExAC
TOPMed
gnomAD
rs1315883832
CA410354940
146 K>M No ClinGen
gnomAD
rs1299623506
CA410354924
148 S>G No ClinGen
gnomAD
CA410354903
rs1442703549
149 V>A No ClinGen
TOPMed
gnomAD
CA410354902
rs1442703549
149 V>G No ClinGen
TOPMed
gnomAD
CA410354870
rs1380809869
152 C>R No ClinGen
gnomAD
TCGA novel 154 S>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs776821544
CA10038924
154 S>N No ClinGen
ExAC
gnomAD
rs776821544
CA321461064
154 S>T No ClinGen
ExAC
gnomAD
rs1240485100
CA410354804
156 N>T No ClinGen
TOPMed
CA321461045
rs1011435687
157 E>K No ClinGen
TOPMed
gnomAD
CA410354761
rs1166628937
158 A>V No ClinGen
TOPMed
gnomAD
rs773046447
CA10038921
159 Q>E No ClinGen
ExAC
gnomAD
CA10038920
rs771941611
161 K>E No ClinGen
ExAC
TOPMed
gnomAD
rs1235327176
CA410354696
162 T>I No ClinGen
gnomAD
TCGA novel 162 T>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410354691
rs1183610194
163 V>I No ClinGen
gnomAD
rs1177929644
CA410354672
164 S>N No ClinGen
TOPMed
rs1315299635
CA410354627
166 N>S No ClinGen
Ensembl
CA410354617
rs1377318498
167 Q>K No ClinGen
TOPMed
rs779713054
CA10038915
169 D>N No ClinGen
ExAC
TOPMed
gnomAD
rs755598764
CA10038914
169 D>V No ClinGen
ExAC
TOPMed
gnomAD
rs1281482427
CA410354526
171 S>R No ClinGen
gnomAD
CA10038913
rs200087612
172 H>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs778144401
CA10038912
173 T>A No ClinGen
ExAC
gnomAD
rs1327210036
CA410354504
173 T>N No ClinGen
gnomAD
CA10038910
rs753169498
175 R>Q Variant assessed as Somatic; 4.619e-05 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs572463453
CA10038911
175 R>W No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs765674209
CA10038909
177 S>C No ClinGen
ExAC
gnomAD
CA10038908
rs755292040
178 P>L No ClinGen
ExAC
gnomAD
CA321460948
rs145945008
178 P>T No ClinGen
ESP
TOPMed
gnomAD
CA10038907
rs369209992
180 I>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs909574651
CA321460936
181 A>T No ClinGen
TOPMed
gnomAD
CA321460929
rs1036973149
182 V>D No ClinGen
Ensembl
CA410354408
rs1362887961
182 V>F No ClinGen
gnomAD
CA410354393
rs1238737067
183 K>E Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
TCGA novel 183 K>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410354376
rs1179703372
184 A>S No ClinGen
gnomAD
CA410354366
rs1481554582
185 N>D No ClinGen
TOPMed
rs871545
CA10038906
VAR_052807
185 N>S No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs760685749
CA10038905
187 N>S No ClinGen
ExAC
gnomAD
CA10038904
rs773278764
189 P>S No ClinGen
ExAC
gnomAD
rs761728849
CA10038903
190 H>D No ClinGen
ExAC
gnomAD
rs1286482552
CA410354314
190 H>R No ClinGen
gnomAD
CA10038902
rs761728849
190 H>Y No ClinGen
ExAC
gnomAD
CA410354306
rs1278007065
191 V>A No ClinGen
TOPMed
gnomAD
CA410354310
rs1350172268
191 V>F No ClinGen
gnomAD
rs1346602116
CA410354301
192 P>R No ClinGen
gnomAD
rs139205397
CA410354303
192 P>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038901
rs139205397
192 P>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 193 K>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs576702708
CA10038900
194 P>L No ClinGen
1000Genomes
ExAC
gnomAD
rs1347590306
CA410354280
195 I>M No ClinGen
gnomAD
rs1309114463
CA410354285
195 I>V No ClinGen
gnomAD
rs1421677933
CA410354273
196 E>D No ClinGen
TOPMed
CA10038899
rs749058958
198 L>H No ClinGen
ExAC
TOPMed
gnomAD
CA410354262
rs749058958
198 L>P No ClinGen
ExAC
TOPMed
gnomAD
rs769419148
CA10038897
199 H>R No ClinGen
ExAC
gnomAD
TCGA novel 201 L>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1049329808
CA321460855
203 L>I No ClinGen
TOPMed
gnomAD
CA10038895
rs148545576
209 P>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA410354183
rs148545576
209 P>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA410354166
rs1198568593
212 S>R No ClinGen
gnomAD
rs370796629
CA321460842
213 S>T No ClinGen
Ensembl
rs871546
CA410354127
218 K>E No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs871546
CA10038892
VAR_052808
218 K>Q No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA410354125
rs1446511859
218 K>T No ClinGen
gnomAD
rs755416833
CA10038891
219 S>A No ClinGen
ExAC
gnomAD
rs959903063
CA321460825
220 L>F No ClinGen
TOPMed
gnomAD
rs959903063
CA410354114
220 L>V No ClinGen
TOPMed
gnomAD
CA410354108
rs1324679673
221 E>K No ClinGen
TOPMed
gnomAD
CA410354109
rs1324679673
221 E>Q No ClinGen
TOPMed
gnomAD
CA410354078
rs1337900438
225 S>C No ClinGen
TOPMed
CA10038889
rs754174232
227 D>A No ClinGen
ExAC
gnomAD
rs754174232
CA321460810
227 D>G No ClinGen
ExAC
gnomAD
CA410354048
rs1258436482
230 N>D No ClinGen
TOPMed
rs766515901
CA10038888
230 N>S No ClinGen
ExAC
TOPMed
gnomAD
CA321460794
rs369512462
233 S>N No ClinGen
ESP
TOPMed
gnomAD
CA321460788
rs1022743019
234 L>S No ClinGen
TOPMed
gnomAD
rs1318123946
CA410354008
236 K>E No ClinGen
gnomAD
rs1470778026
CA410353999
237 R>K No ClinGen
gnomAD
TCGA novel 239 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs767565879
CA10038885
240 V>M No ClinGen
ExAC
gnomAD
rs1412547877
CA410353951
244 K>M No ClinGen
gnomAD
rs1569106160
CA410353943
245 P>L No ClinGen
Ensembl
CA10038884
rs761782176
247 Q>P No ClinGen
ExAC
gnomAD
CA321460755
rs768314235
248 D>E No ClinGen
TOPMed
rs116512504
CA10038883
249 R>I No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs954143562
CA321460739
250 E>Q No ClinGen
TOPMed
gnomAD
CA410353908
rs1246306943
251 A>S No ClinGen
gnomAD
rs201645576
CA10038882
252 M>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038881
rs534420079
253 D>G No ClinGen
1000Genomes
ExAC
gnomAD
rs565812774
CA10038880
254 D>G No ClinGen
1000Genomes
ExAC
gnomAD
CA10038879
rs759203459
257 G>D No ClinGen
ExAC
gnomAD
CA10038878
rs759203459
257 G>V No ClinGen
ExAC
gnomAD
rs1309648760
CA410353823
259 S>N No ClinGen
gnomAD
rs925214198
CA321460707
260 G>C No ClinGen
gnomAD
rs776320074
CA10038877
262 L>F No ClinGen
ExAC
TOPMed
gnomAD
rs776320074
CA410353785
262 L>I No ClinGen
ExAC
TOPMed
gnomAD
CA10038875
rs746468965
265 G>E No ClinGen
ExAC
gnomAD
rs1294700503
CA410353749
265 G>R No ClinGen
gnomAD
rs779577202
CA10038874
266 K>T No ClinGen
ExAC
gnomAD
CA410353716
rs1301909418
267 A>D No ClinGen
gnomAD
CA10038872
rs749684515
268 L>P No ClinGen
ExAC
gnomAD
CA10038873
rs563813569
268 L>V No ClinGen
ExAC
gnomAD
rs1569106010
CA410353700
269 E>Q No ClinGen
Ensembl
CA10038871
rs780455947
271 A>V No ClinGen
ExAC
gnomAD
CA10038870
rs200936908
CA10038869
273 K>N No ClinGen
1000Genomes
ExAC
gnomAD
CA410353604
rs1445321667
275 P>L No ClinGen
gnomAD
CA410353602
rs372250863
276 R>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038867
rs368914741
276 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA10038868
rs372250863
276 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1233862365
CA410353575
278 P>A No ClinGen
gnomAD
rs1233862365
CA410353572
278 P>S No ClinGen
gnomAD
CA410353526
rs1247454035
280 L>F No ClinGen
TOPMed
gnomAD
rs762933040
CA10038864
280 L>S No ClinGen
ExAC
gnomAD
rs915836
CA10038863
282 V>I No ClinGen
ExAC
TOPMed
gnomAD
rs374842935
CA410353490
283 C>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs759211921
CA10038861
283 C>R No ClinGen
ExAC
gnomAD
rs374842935
CA10038860
283 C>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA321460526
rs775456657
287 E>Q No ClinGen
gnomAD
CA10038858
rs760266610
289 P>R No ClinGen
ExAC
gnomAD
rs371804389
CA10038855
290 Y>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 291 L>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410353318
rs1421051378
292 L>S No ClinGen
gnomAD
rs770229750
CA10038853
292 L>V No ClinGen
ExAC
gnomAD
CA10038851
rs781393923
293 K>Q No ClinGen
ExAC
gnomAD
rs751692990
CA10038849
294 E>K No ClinGen
ExAC
gnomAD
rs139961876
CA10038848
296 N>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs752710665
CA10038846
300 G>D No ClinGen
ExAC
gnomAD
TCGA novel 300 G>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs765035883
CA10038845
301 Q>H No ClinGen
ExAC
gnomAD
CA10038844
rs201785777
302 G>V No ClinGen
1000Genomes
ExAC
gnomAD
CA10038841
rs760392970
304 D>G No ClinGen
ExAC
TOPMed
gnomAD
CA10038842
rs766203038
304 D>H No ClinGen
ExAC
gnomAD
rs1285113722
CA410353085
305 R>T No ClinGen
gnomAD
CA410353026
rs1390085999
307 L>F No ClinGen
gnomAD
CA10038840
rs772900332
307 L>W No ClinGen
ExAC
gnomAD
rs767025452
CA10038838
310 Y>C No ClinGen
ExAC
gnomAD
rs1345948808
CA410352983
310 Y>H No ClinGen
TOPMed
gnomAD
rs761192288
CA10038837
311 S>A No ClinGen
ExAC
gnomAD
CA10038836
rs776091446
312 K>E No ClinGen
ExAC
gnomAD
rs370927013
CA10038835
312 K>R No ClinGen
ExAC
gnomAD
rs1289527818
CA410352902
314 G>S No ClinGen
gnomAD
rs113844596
CA321460332
314 G>V No ClinGen
Ensembl
CA410352883
rs1418787184
315 L>I No ClinGen
TOPMed
rs771189468
CA10038832
316 V>G No ClinGen
ExAC
gnomAD
CA410352816
rs747199104
318 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA10038831
rs747199104
318 P>R No ClinGen
ExAC
TOPMed
gnomAD
CA410352811
rs1445578357
319 S>P No ClinGen
TOPMed
rs777816360
CA10038830
322 S>P No ClinGen
ExAC
gnomAD
CA321460304
rs143307999
324 S>P No ClinGen
ESP
TOPMed
gnomAD
rs1264831868
CA410352698
328 S>N No ClinGen
gnomAD
CA10038828
rs748118040
328 S>R No ClinGen
ExAC
gnomAD
rs149159484
CA10038826
329 I>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038827
rs778915166
329 I>V No ClinGen
ExAC
gnomAD
CA410352673
rs1470531718
330 D>V No ClinGen
gnomAD
CA410352669
rs1601635543
331 R>G No ClinGen
Ensembl
rs1383981304
CA410352652
332 S>N No ClinGen
TOPMed
gnomAD
CA410352627
rs1307257523
335 L>V No ClinGen
TOPMed
CA410352615
rs1320102266
336 V>A No ClinGen
gnomAD
CA410352591
rs1353082651
338 S>T No ClinGen
TOPMed
rs766256414
CA10038824
340 L>I No ClinGen
ExAC
gnomAD
TCGA novel 340 L>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs925079256
CA321460273
341 R>I No ClinGen
Ensembl
CA10038821
rs767033947
342 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs750124231
CA10038823
342 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs931927912
CA321460248
346 M>L No ClinGen
Ensembl
rs921869044
CA321460243
347 D>G No ClinGen
Ensembl
rs748660139
CA10038817
349 Q>L No ClinGen
ExAC
TOPMed
gnomAD
CA410352448
rs1187521330
350 V>F No ClinGen
gnomAD
TCGA novel 351 P>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1177314405
CA410352429
352 V>I No ClinGen
TOPMed
rs150447458
CA10038815
353 Y>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1244595246
CA410352381
355 P>L No ClinGen
TOPMed
gnomAD
rs1244595246
CA410352383
355 P>R No ClinGen
TOPMed
gnomAD
rs1438561654
CA410352387
355 P>S No ClinGen
TOPMed
CA410352379
rs1409758647
356 S>A No ClinGen
TOPMed
rs1229570769
CA410352354
357 I>T No ClinGen
gnomAD
CA321460206
rs1015437087
357 I>V No ClinGen
TOPMed
gnomAD
CA10038813
rs773488868
359 L>F No ClinGen
ExAC
gnomAD
rs976840377
CA321460201
359 L>M No ClinGen
TOPMed
TCGA novel 360 K>E Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10038811
rs748317140
363 Q>H No ClinGen
ExAC
TOPMed
gnomAD
rs140723466
CA321460171
363 Q>L No ClinGen
ESP
TOPMed
TCGA novel 363 Q>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 365 S>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410352246
rs1337655651
366 S>P No ClinGen
gnomAD
CA10038809
COSM2819275
rs367715997
367 S>L pancreas [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
gnomAD
rs756000272
CA10038806
368 V>L No ClinGen
ExAC
gnomAD
CA10038805
rs750114432
369 S>Y No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 370 S>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1167376763
CA410352169
372 A>G No ClinGen
gnomAD
rs1386687361
CA410352163
373 P>S No ClinGen
gnomAD
CA410352150
rs1187868447
374 G>A No ClinGen
TOPMed
gnomAD
rs1187868447
CA410352151
374 G>E No ClinGen
TOPMed
gnomAD
CA410352152
rs1365818706
374 G>W No ClinGen
TOPMed
CA10038803
rs146864981
378 C>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs186427345
CA10038802
378 C>Y No ClinGen
1000Genomes
ExAC
gnomAD
CA10038798
rs766805673
382 Q>R No ClinGen
ExAC
TOPMed
gnomAD
CA10038797
rs374656028
384 S>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1309526242
CA410352013
385 S>C No ClinGen
gnomAD
CA10038796
rs773435350
385 S>T No ClinGen
ExAC
gnomAD
rs1392334282
CA410351973
388 D>G No ClinGen
gnomAD
CA410351957
rs1370437101
389 C>F No ClinGen
gnomAD
rs1026612034
CA410351963
389 C>G No ClinGen
TOPMed
gnomAD
rs1026612034
CA321460043
389 C>S No ClinGen
TOPMed
gnomAD
CA410351935
rs1306776246
391 E>D No ClinGen
TOPMed
gnomAD
rs748586028
CA10038795
392 K>E No ClinGen
ExAC
TOPMed
gnomAD
rs1366973259
CA410351929
392 K>I No ClinGen
gnomAD
CA10038794
rs375045369
393 T>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1470847039
CA410351926
393 T>P No ClinGen
TOPMed
TCGA novel 393 T>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410351923
rs375045369
393 T>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs774537436
CA10038793
397 D>N No ClinGen
ExAC
CA410351895
rs1366358306
398 R>G No ClinGen
gnomAD
CA321460011
rs952197943
399 P>L No ClinGen
TOPMed
CA10038792
rs768876767
400 Q>E No ClinGen
ExAC
gnomAD
CA10038790
rs780140400
403 Q>K No ClinGen
ExAC
gnomAD
rs769792057
CA10038789
404 P>L No ClinGen
ExAC
TOPMed
gnomAD
rs769792057
CA410351855
404 P>Q No ClinGen
ExAC
TOPMed
gnomAD
rs201511548
CA10038787
405 H>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1569105102
CA410351850
405 H>Y No ClinGen
Ensembl
COSM1682004
rs866691451
CA321459969
406 R>C haematopoietic_and_lymphoid_tissue [Cosmic] No ClinGen
cosmic curated
gnomAD
CA10038785
rs534651803
COSM1030970
406 R>H Variant assessed as Somatic; 0.0 impact. endometrium haematopoietic_and_lymphoid_tissue [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ExAC
NCI-TCGA
CA410351839
rs1601634729
407 L>F No ClinGen
Ensembl
CA410351836
rs1240186781
407 L>R No ClinGen
gnomAD
CA410351817
rs1601634688
410 F>C No ClinGen
Ensembl
CA10038781
rs757909132
412 A>V No ClinGen
ExAC
gnomAD
CA321459946
rs906129974
413 S>A No ClinGen
Ensembl
rs761081806
CA10038778
416 T>A Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
CA410351767
rs1569104992
418 R>T No ClinGen
Ensembl
rs779562322
CA321459923
418 R>W No ClinGen
Ensembl
CA410351763
rs1169584905
419 E>K No ClinGen
TOPMed
CA410351762
rs1169584905
419 E>Q No ClinGen
TOPMed
CA321459916
rs986050311
420 G>R No ClinGen
TOPMed
CA10038776
rs1555910490
421 A>D No ClinGen
Ensembl
rs1453816344
CA410351740
422 S>F No ClinGen
TOPMed
gnomAD
rs1367739212
CA410351735
423 P>R No ClinGen
TOPMed
CA410351723
rs1159987871
425 T>S No ClinGen
gnomAD
rs1457544605
CA410351713
427 V>M No ClinGen
gnomAD
CA321459891
rs1013681104
428 R>C No ClinGen
TOPMed
gnomAD
rs767749393
CA10038774
428 R>H No ClinGen
ExAC
TOPMed
gnomAD
rs767749393
CA321459883
428 R>L No ClinGen
ExAC
TOPMed
gnomAD
rs774742814
CA410351699
429 I>M No ClinGen
ExAC
gnomAD
CA10038773
rs762186664
429 I>V No ClinGen
ExAC
TOPMed
gnomAD
rs768929656
CA10038771
430 K>R No ClinGen
ExAC
gnomAD
rs763134143
CA10038770
432 E>G No ClinGen
ExAC
gnomAD
CA10038768
rs769896114
436 P>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA410351648
rs1261938102
437 L>P No ClinGen
TOPMed
CA10038765
rs565521840
438 S>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1601634343
CA410351637
439 D>A No ClinGen
Ensembl
CA10038762
rs758033755
441 S>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs1569104827
CA410351622
442 D>N No ClinGen
Ensembl
TCGA novel 443 I>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410351613
rs1170489222
443 I>V No ClinGen
TOPMed
gnomAD
rs1601634294
CA410351606
444 I>V No ClinGen
Ensembl
COSM1030968
CA10038760
rs778362506
445 R>C Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA410351598
rs1387467282
445 R>H No ClinGen
TOPMed
gnomAD
CA10038758
rs200548353
446 V>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs757564523
CA10038756
447 T>A No ClinGen
ExAC
gnomAD
CA410351586
rs1569104767
447 T>I No ClinGen
Ensembl
CA410351575
rs1243978192
449 G>A No ClinGen
gnomAD
CA410351574
rs1243978192
449 G>E No ClinGen
gnomAD
rs1332574453
CA410351570
450 D>G No ClinGen
TOPMed
CA10038754
rs764464700
450 D>N No ClinGen
ExAC
TOPMed
gnomAD
CA10038751
rs146658168
451 A>E No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038752
rs146658168
451 A>G No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA321459746
rs373472839
451 A>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038753
rs373472839
451 A>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038750
rs146658168
451 A>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs770844928
CA10038748
452 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs138612343
CA10038747
453 T>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1342242255
CA410351554
454 T>A No ClinGen
gnomAD
CA410351544
rs1481717171
455 A>V No ClinGen
TOPMed
gnomAD
CA10038744
rs771751501
456 A>P No ClinGen
ExAC
CA410351536
rs1441833377
457 A>T No ClinGen
TOPMed
rs1569104626
CA410351532
458 S>T No ClinGen
Ensembl
CA410351523
rs1184135041
459 S>C No ClinGen
TOPMed
rs747775406
CA10038743
459 S>P No ClinGen
ExAC
gnomAD
CA10038742
rs778486875
460 S>L No ClinGen
ExAC
TOPMed
gnomAD
rs144046665
CA410351514
461 S>* No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038739
rs144046665
461 S>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038740
rs748762686
461 S>P No ClinGen
ExAC
TOPMed
gnomAD
rs200368573
CA321459671
463 T>A No ClinGen
Ensembl
rs1412630339
CA410351502
463 T>I No ClinGen
gnomAD
CA321459627
rs983442942
465 D>E No ClinGen
Ensembl
rs1569104545
CA410351493
465 D>H No ClinGen
Ensembl
CA10038734
rs764534410
466 L>P No ClinGen
ExAC
gnomAD
TCGA novel 467 S>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1199911146
CA410351458
470 T>I No ClinGen
Ensembl
rs1601633895
CA410351443
472 D>E No ClinGen
Ensembl
rs1240737716
CA410351435
473 D>E No ClinGen
TOPMed
CA410351440
rs1185702965
473 D>H No ClinGen
gnomAD
rs1237324920
CA410351429
474 Q>R No ClinGen
gnomAD
rs765434781
CA10038730
475 K>E No ClinGen
ExAC
gnomAD
CA10038729
rs759549499
476 D>G No ClinGen
ExAC
gnomAD
CA10038726
rs547367731
CA410351406
477 M>I No ClinGen
1000Genomes
ExAC
TOPMed
rs766294586
CA10038727
477 M>T No ClinGen
ExAC
gnomAD
CA410351410
rs1205186914
477 M>V No ClinGen
gnomAD
CA410351402
rs1204007027
478 S>G No ClinGen
TOPMed
CA410351386
rs375747565
480 L>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA410351387
rs1327216115
480 L>I No ClinGen
TOPMed
gnomAD
rs375747565
CA10038724
480 L>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA321459551
rs372739397
482 A>V No ClinGen
ESP
CA10038723
rs199629325
483 K>E No ClinGen
1000Genomes
ExAC
gnomAD
rs1398150781
CA410351357
485 R>K No ClinGen
gnomAD
CA10038722
rs773876783
488 A>T No ClinGen
ExAC
gnomAD
CA410351332
rs1372278157
488 A>V No ClinGen
gnomAD
rs921242245
CA410351323
490 R>G No ClinGen
TOPMed
gnomAD
CA10038719
rs531808521
490 R>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA10038718
rs531808521
490 R>Q No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
TCGA novel 491 R>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1424556249
CA410351309
492 L>W No ClinGen
gnomAD
CA410351304
rs1413349976
493 P>S No ClinGen
gnomAD
rs61751934
CA410351293
494 F>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038715
rs758841154
495 K>R No ClinGen
ExAC
TOPMed
gnomAD
CA410351210
rs1182179559
499 V>M No ClinGen
TOPMed
gnomAD
rs1271789230
CA410351193
500 N>T No ClinGen
gnomAD
CA10038713
rs779062134
501 E>A No ClinGen
ExAC
gnomAD
CA410351182
rs1321908078
501 E>K No ClinGen
gnomAD
rs766460973
CA10038710
503 G>A No ClinGen
ExAC
gnomAD
CA10038711
rs200969667
503 G>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA321459484
rs903638899
504 S>C No ClinGen
TOPMed
gnomAD
CA410351134
rs903638899
504 S>F No ClinGen
TOPMed
gnomAD
rs771472213
CA321459473
505 P>A No ClinGen
Ensembl
rs767373661
CA10038707
506 V>M No ClinGen
ExAC
CA321459447
rs991716183
507 S>T No ClinGen
TOPMed
gnomAD
rs1266983823
CA410351060
510 N>D No ClinGen
TOPMed
CA410351028
rs1349462862
512 E>Q No ClinGen
gnomAD
rs186141325
CA10038704
513 E>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA10038705
rs761608135
513 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs1477660116
CA410350999
514 G>D No ClinGen
TOPMed
CA321459410
rs958958319
514 G>S No ClinGen
TOPMed
gnomAD
rs1477660116
CA410350996
514 G>V No ClinGen
TOPMed
rs1171745212
CA410350966
517 P>T No ClinGen
TOPMed
CA410350955
rs1181927407
518 T>A No ClinGen
TOPMed
gnomAD
rs1181927407
CA410350956
518 T>P No ClinGen
TOPMed
gnomAD
rs1471860456
CA410350950
518 T>S No ClinGen
gnomAD
rs369562728
CA10038703
519 L>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs774961135
CA10038701
520 L>H No ClinGen
ExAC
gnomAD
rs1364626816
CA410350917
521 D>V No ClinGen
TOPMed
rs35124464
CA10038699
522 A>G No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs769463187
CA10038700
522 A>T No ClinGen
ExAC
gnomAD
CA410350907
rs35124464
522 A>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs778439560
CA10038698
523 D>G No ClinGen
ExAC
TOPMed
gnomAD
rs1268460915
CA410350890
524 F>L No ClinGen
TOPMed
gnomAD
CA10038697
rs772695794
526 D>H No ClinGen
ExAC
gnomAD
CA321459364
rs1047783924
527 S>C No ClinGen
Ensembl
CA10038696
rs538355517
527 S>P No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs575685431
CA10038694
COSM3423967
533 E>K Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
TCGA novel 535 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10038693
rs754112732
535 G>S No ClinGen
ExAC
gnomAD
CA410350709
rs1569103825
537 L>F No ClinGen
Ensembl
CA10038691
rs756188749
539 G>E No ClinGen
ExAC
TOPMed
gnomAD
CA10038690
rs750441789
540 T>A No ClinGen
ExAC
gnomAD
rs369867786
CA10038688
540 T>M No ClinGen
1000Genomes
ESP
TOPMed
gnomAD
rs369867786
CA321459344
540 T>R No ClinGen
1000Genomes
ESP
TOPMed
gnomAD
CA321459336
rs372989729
543 N>S No ClinGen
Ensembl
CA410350632
rs1177476611
544 K>* No ClinGen
TOPMed
gnomAD
CA410350587
rs1288583562
546 F>C No ClinGen
gnomAD
CA410350583
rs1423925254
546 F>L No ClinGen
gnomAD
CA321459326
rs1050241683
548 C>W No ClinGen
TOPMed
CA321459319
rs536489413
549 K>R No ClinGen
1000Genomes
gnomAD
CA410350540
rs1403884085
550 H>P No ClinGen
TOPMed
gnomAD
CA410350534
rs1363345264
550 H>Q No ClinGen
TOPMed
gnomAD
rs377174109
CA10038687
550 H>Y No ClinGen
ESP
ExAC
gnomAD
CA10038685
rs751347821
553 K>M No ClinGen
ExAC
TOPMed
gnomAD
CA10038686
rs751347821
553 K>R No ClinGen
ExAC
TOPMed
gnomAD
rs1569103726
CA410350491
554 I>V No ClinGen
Ensembl
rs1463414560
CA410350460
556 R>K No ClinGen
gnomAD
rs763975633
CA10038684
558 T>S No ClinGen
ExAC
gnomAD
TCGA novel 559 A>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410350381
rs1311550047
563 R>C No ClinGen
gnomAD
CA410350382
rs1311550047
563 R>G No ClinGen
gnomAD
CA10038683
rs762620358
563 R>H No ClinGen
ExAC
TOPMed
gnomAD
CA10038682
rs775215972
564 H>D No ClinGen
ExAC
gnomAD
rs769516477
CA10038681
567 M>I No ClinGen
ExAC
TOPMed
gnomAD
CA410350332
rs1363748550
568 Y>F No ClinGen
TOPMed
rs1394078337
CA410350308
571 P>L No ClinGen
TOPMed
rs776278980
CA10038679
576 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA10038676
rs779238448
579 I>M No ClinGen
ExAC
gnomAD
CA10038674
rs749547579
581 H>L No ClinGen
ExAC
gnomAD
CA10038675
rs769094396
581 H>Y No ClinGen
ExAC
gnomAD
CA321459248
rs908569698
583 R>G No ClinGen
TOPMed
gnomAD
TCGA novel 583 R>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 583 R>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10038673
rs780264567
586 T>N No ClinGen
ExAC
gnomAD
CA410350196
rs1244349021
587 N>T No ClinGen
TOPMed
rs1456224652
CA410350136
595 Q>R No ClinGen
Ensembl
CA410350115
rs1569103535
598 H>P No ClinGen
Ensembl
rs376613040
CA10038671
599 G>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038670
rs746009629
600 I>V No ClinGen
ExAC
gnomAD
rs1244193796
CA410350099
601 V>L No ClinGen
TOPMed
rs371648001
CA10038669
602 K>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1343017109
CA410350067
605 S>L No ClinGen
gnomAD
CA10038667
rs751551584
606 P>A Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1313798631
CA410350052
608 S>Y No ClinGen
gnomAD
CA10038665
rs533820608
609 S>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs993399269
CA321459201
616 E>D No ClinGen
Ensembl
CA410349979
rs752422141
618 F>L No ClinGen
ExAC
TOPMed
gnomAD
rs956330951
CA321459175
619 Q>R No ClinGen
Ensembl
rs765051299
CA10038663
625 I>V No ClinGen
ExAC
TOPMed
gnomAD
CA10038661
rs759233505
628 E>D No ClinGen
ExAC
gnomAD
TCGA novel 630 E>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410349903
rs776330374
630 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs776330374
CA10038660
630 E>Q No ClinGen
ExAC
TOPMed
gnomAD
rs769060928 631 I>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10038658
rs766009068
631 I>T No ClinGen
ExAC
gnomAD
rs760064273
CA10038657
634 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs774925674
CA10038656
636 I>F No ClinGen
ExAC
gnomAD
CA410349862
rs1569103403
636 I>T No ClinGen
Ensembl
rs1483416554
CA410349854
637 I>N No ClinGen
gnomAD
CA321459118
rs981751404
638 K>M No ClinGen
TOPMed
CA410349845
rs1273936269
638 K>N No ClinGen
TOPMed
gnomAD
CA10038655
rs768986339
640 R>K No ClinGen
ExAC
gnomAD
CA10038654
rs368176716
641 R>C Variant assessed as Somatic; 0.000231 impact. [NCI-TCGA] No ClinGen
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs181765349
CA10038653
641 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
CA10038650
rs374257072
642 G>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1350419272
CA410349812
644 P>A No ClinGen
TOPMed
gnomAD
CA410349804
rs1343219190
645 G>D No ClinGen
gnomAD
CA410349782
rs1306834060
648 G>A No ClinGen
gnomAD
rs757366582
CA10038649
650 S>R No ClinGen
ExAC
TOPMed
gnomAD
CA321459067
rs563008699
652 S>P No ClinGen
1000Genomes
gnomAD
rs1315614436
CA410349744
654 A>T No ClinGen
gnomAD
rs747005842
CA10038648
655 Q>R No ClinGen
ExAC
gnomAD
rs777827111
CA10038647
657 V>G No ClinGen
ExAC
gnomAD
rs758265763
CA10038646
658 I>V No ClinGen
ExAC
gnomAD
CA410349710
rs1161120720
659 K>E No ClinGen
gnomAD
CA10038644
rs765102550
660 R>S No ClinGen
ExAC
TOPMed
gnomAD
CA10038643
rs754770060
661 N>S No ClinGen
ExAC
TOPMed
gnomAD
CA410349688
rs1470842185
662 L>S No ClinGen
TOPMed
rs1268273304
CA410349670
665 R>* No ClinGen
gnomAD
rs1383789184
CA410349669
665 R>Q No ClinGen
gnomAD
rs753575876
CA10038642
667 K>R No ClinGen
ExAC
gnomAD
rs1329479530
CA410349630
671 I>T No ClinGen
TOPMed
CA10038641
rs765879473
671 I>V No ClinGen
ExAC
gnomAD
rs1287063990
CA638058052
674 Y>* No ClinGen
gnomAD
rs900240287
CA321459023
674 Y>* No ClinGen
Ensembl
CA10038639
rs549192072
674 Y>C No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA410349606
rs1439357201
675 C>R No ClinGen
gnomAD
CA410349607
rs1439357201
675 C>S No ClinGen
gnomAD
rs763333388
CA10038637
676 G>R No ClinGen
ExAC
TOPMed
gnomAD
CA321459021
rs868358292
677 K>E No ClinGen
Ensembl
COSM1289111
rs775878367
CA10038636
678 A>V Variant assessed as Somatic; 0.0 impact. autonomic_ganglia [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs775366778
CA10038633
679 Y>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA10038632
rs371004245
680 R>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs763079412
CA10038631
680 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1479043549
CA410349570
681 F>V No ClinGen
TOPMed
gnomAD
rs772096023
CA10038629
684 Q>R No ClinGen
ExAC
TOPMed
rs1475124769
CA410349527
687 Q>E No ClinGen
gnomAD
CA321458953
rs1047649873
689 I>M No ClinGen
Ensembl
rs1198264194
CA410349511
689 I>V No ClinGen
gnomAD
CA10038627
rs748120189
690 K>E No ClinGen
ExAC
gnomAD
TCGA novel 691 M>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10038626
rs189444051
691 M>I No ClinGen
1000Genomes
ExAC
gnomAD
rs1209730709
CA410349467
694 G>V No ClinGen
gnomAD
CA10038625
rs540935593
697 P>S No ClinGen
1000Genomes
ExAC
gnomAD
rs374478553
CA10038623
701 N>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 703 V>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA321458890
rs920554378
703 V>I No ClinGen
gnomAD
rs1231928012
CA410349315
707 K>E No ClinGen
TOPMed
gnomAD
rs948865923
CA321458878
708 E>A No ClinGen
Ensembl
rs766911585
CA10038618
709 H>Y No ClinGen
ExAC
gnomAD
rs769735934
CA321458861
711 P>H No ClinGen
TOPMed
CA321458857
rs769735934
711 P>L No ClinGen
TOPMed
rs769735934
CA321458859
711 P>R No ClinGen
TOPMed
rs201379071
CA10038616
711 P>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs201379071
CA10038617
711 P>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1316112483
CA410349248
712 L>F No ClinGen
gnomAD
CA10038615
rs748296477
715 P>A No ClinGen
ExAC
TOPMed
gnomAD
CA10038614
rs148103348
715 P>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA321458853
rs748296477
715 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs1353427850
CA410348489
718 N>D No ClinGen
Ensembl
rs771225314
CA10038612
718 N>K No ClinGen
ExAC
gnomAD
rs760786843
CA10038611
719 K>E No ClinGen
ExAC
TOPMed
gnomAD
CA410348479
rs760786843
719 K>Q No ClinGen
ExAC
TOPMed
gnomAD
CA410348450
rs1202145282
721 V>F No ClinGen
TOPMed
gnomAD
CA410348452
rs1202145282
721 V>L No ClinGen
TOPMed
gnomAD
rs1055929176
CA321458822
723 Q>* No ClinGen
TOPMed
CA10038607
rs772077056
723 Q>R No ClinGen
ExAC
gnomAD
rs748169707
CA10038606
724 C>R No ClinGen
ExAC
gnomAD
rs779007688
CA10038605
724 C>Y No ClinGen
ExAC
rs781158471
CA10038604
725 R>C No ClinGen
ExAC
gnomAD
CA10038603
rs749159583
725 R>H No ClinGen
ExAC
TOPMed
gnomAD
CA410348394
rs1299351917
726 L>F No ClinGen
gnomAD
rs1269950227
CA410348356
729 A>T No ClinGen
TOPMed
rs779678782
CA10038602
729 A>V No ClinGen
ExAC
gnomAD
rs1360851210
CA410348337
731 L>V No ClinGen
gnomAD
COSM579354
rs1340971024
CA410348323
732 S>C lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs1340971024
CA410348324
732 S>F No ClinGen
gnomAD
CA10038601
rs755837122
732 S>P No ClinGen
ExAC
gnomAD
CA410348317
rs1333479266
733 S>P No ClinGen
gnomAD
CA410348255
rs1169318240
738 G>E No ClinGen
gnomAD
CA410348261
rs1372553865
738 G>R No ClinGen
gnomAD
rs143766083
CA10038599
COSM1233854
741 E>K large_intestine [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs143766083
CA321458761
741 E>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs756776510
CA10038598
742 R>Q No ClinGen
ExAC
gnomAD
rs978961345
COSM1233857
CA321458751
742 R>W large_intestine [Cosmic] No ClinGen
cosmic curated
TOPMed
gnomAD
CA410348200
rs1221087736
743 L>P No ClinGen
TOPMed
rs1237380022
CA410348193
744 C>G No ClinGen
gnomAD
rs370495247
CA10038596
745 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038597
rs372605163
745 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs766677597
CA10038594
747 A>S No ClinGen
ExAC
TOPMed
gnomAD
rs766677597
CA10038593
747 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs761062800
CA10038592
747 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA410348154
rs1356873285
748 A>G No ClinGen
gnomAD
CA10038588
rs774567286
COSM3405404
749 V>I Variant assessed as Somatic; 0.0001849 impact. central_nervous_system [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs768750113
CA10038587
752 Y>F No ClinGen
ExAC
TOPMed
gnomAD
rs749212154
CA10038586
754 S>I No ClinGen
ExAC
TOPMed
gnomAD
rs1018797607
CA321458652
755 L>F No ClinGen
TOPMed
CA10038584
rs780395187
756 R>G No ClinGen
ExAC
gnomAD
rs1601631611
CA410348060
757 F>V No ClinGen
Ensembl
CA10038583
rs745621195
758 F>S No ClinGen
ExAC
gnomAD
CA10038582
rs140690647
759 S>L No ClinGen
ESP
ExAC
gnomAD
rs757855811
CA10038578
COSM1271251
761 E>K Variant assessed as Somatic; 0.0 impact. oesophagus [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs754335990
CA10038577
761 E>V No ClinGen
ExAC
gnomAD
rs372891692
CA321458591
762 L>V No ClinGen
ESP
TOPMed
gnomAD
CA10038576
rs148869512
763 K>N No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1291827952
CA410347975
763 K>Q No ClinGen
TOPMed
rs756447548
CA10038575
764 Q>E No ClinGen
ExAC
gnomAD
rs1569102543
CA410347944
764 Q>H No ClinGen
Ensembl
rs750786740
CA10038574
764 Q>R No ClinGen
ExAC
gnomAD
rs886365479
CA321458555
766 H>D No ClinGen
TOPMed
rs146730935
CA10038572
767 E>G No ClinGen
1000Genomes
ExAC
gnomAD
CA410347916
rs767916697
767 E>K No ClinGen
ExAC
TOPMed
gnomAD
CA10038573
rs767916697
767 E>Q No ClinGen
ExAC
TOPMed
gnomAD
CA321458547
rs995504957
768 S>T No ClinGen
TOPMed
rs1223261407
CA410347878
769 K>M No ClinGen
gnomAD
CA410347887
rs1288961472
769 K>Q No ClinGen
gnomAD
CA410347849
rs1295491383
771 E>G No ClinGen
gnomAD
rs764288916
CA10038570
772 Y>C No ClinGen
ExAC
gnomAD
rs764288916
CA10038571
772 Y>F No ClinGen
ExAC
gnomAD
rs1601631392
CA410347826
773 K>R No ClinGen
Ensembl
CA410347802
rs1324251521
775 L>V No ClinGen
gnomAD
rs1601631370
CA410347794
776 T>P No ClinGen
Ensembl
rs1459174790
CA410347780
777 C>Y No ClinGen
gnomAD
rs150534082
COSM109913
CA10038568
778 L>F skin [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
rs769759741
CA321458527
779 E>K No ClinGen
ExAC
gnomAD
rs769759741
CA10038567
779 E>Q No ClinGen
ExAC
gnomAD
CA410347727
rs1192434800
781 M>K No ClinGen
gnomAD
CA10038565
rs750022976
781 M>V No ClinGen
ExAC
TOPMed
gnomAD
rs770619374
CA10038564
782 R>C No ClinGen
ExAC
gnomAD
COSM1414232
rs1252017088
CA410347709
782 R>H Variant assessed as Somatic; 0.0 impact. large_intestine haematopoietic_and_lymphoid_tissue [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs777366464
CA10038562
785 K>R No ClinGen
ExAC
TOPMed
gnomAD
CA410347657
rs1268685369
786 S>F No ClinGen
gnomAD
CA410347666
rs1466118525
786 S>T No ClinGen
gnomAD
TCGA novel 787 S>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs757909218
CA10038561
788 F>V No ClinGen
ExAC
gnomAD
CA321458475
rs907348239
790 I>L No ClinGen
TOPMed
gnomAD
CA321458486
rs907348239
790 I>V No ClinGen
TOPMed
gnomAD
CA410347585
rs1370460084
792 R>Q No ClinGen
gnomAD
rs1219915702
COSM1030964
CA410347587
792 R>W Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
CA410347546
rs1301578722
795 V>F No ClinGen
TOPMed
gnomAD
CA410347550
rs1301578722
795 V>I No ClinGen
TOPMed
gnomAD
rs1569102331
CA410347519
797 V>A No ClinGen
Ensembl
rs1335114617
CA410347510
798 H>R No ClinGen
TOPMed
CA10038559
rs780481918
802 N>S No ClinGen
ExAC
gnomAD
rs1238350647
CA410347425
803 M>T No ClinGen
gnomAD
rs1288674520
CA410347434
803 M>V No ClinGen
gnomAD
rs775667455
CA321458466
804 A>S No ClinGen
Ensembl
CA10038558
rs756639382
805 P>S No ClinGen
ExAC
gnomAD
CA410347384
rs756639382
805 P>T No ClinGen
ExAC
gnomAD
CA410347360
rs1454374570
806 T>I No ClinGen
gnomAD
CA10038556
rs374335079
COSM188356
807 E>K large_intestine Variant assessed as Somatic; 4.619e-05 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA321458438
rs778668120
808 N>K Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA10038555
rs757643691
809 F>L No ClinGen
ExAC
TOPMed
gnomAD
rs895930108
CA321458432
810 S>P No ClinGen
Ensembl
CA10038552
rs764342132
811 L>F No ClinGen
ExAC
gnomAD
CA410347269
rs1236256494
811 L>M No ClinGen
TOPMed
rs751859471
CA10038553
811 L>S No ClinGen
ExAC
TOPMed
gnomAD
rs763003881
CA10038551
812 P>T No ClinGen
ExAC
TOPMed
gnomAD
rs924745278
CA410347231
813 V>F No ClinGen
TOPMed
gnomAD
rs924745278
CA321458423
813 V>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA10038548
rs141394564
817 N>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA410347101
rs770744034
819 D>H No ClinGen
ExAC
gnomAD
CA10038546
rs770744034
819 D>N No ClinGen
ExAC
gnomAD
rs1434793452
CA410347084
819 D>V No ClinGen
gnomAD
rs1204488413
CA410347025
822 G>D No ClinGen
TOPMed
CA10038545
rs760398117
826 P>A No ClinGen
ExAC
gnomAD
rs371914276
CA10038543
827 Q>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038541
rs778453601
828 S>P No ClinGen
ExAC
gnomAD
CA410346763
rs1364510078
833 N>D No ClinGen
TOPMed
CA410346730
rs1192137478
833 N>I No ClinGen
gnomAD
CA10038540
rs770249592
833 N>K No ClinGen
ExAC
TOPMed
gnomAD
CA321458334
rs974462394
835 V>L No ClinGen
Ensembl
CA410346626
rs1258181102
837 H>Y No ClinGen
gnomAD
rs368742609
CA10038539
838 I>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1601630785
CA410346556
839 V>A No ClinGen
Ensembl
rs553654791
CA10038536
839 V>F No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs553654791
CA10038537
839 V>I No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA10038535
rs778210526
840 T>P No ClinGen
ExAC
TOPMed
gnomAD
CA10038533
rs534093710
841 T>R No ClinGen
1000Genomes
ExAC
gnomAD
rs1225663965
CA410346458
843 D>G No ClinGen
gnomAD
CA10038531
rs759494359
844 D>N No ClinGen
ExAC
gnomAD
CA10038530
rs753781623
845 N>H No ClinGen
ExAC
rs766247343
CA10038529
845 N>S No ClinGen
ExAC
gnomAD
CA410346408
rs1389372941
846 V>A No ClinGen
TOPMed
rs868401998
CA321458231
846 V>M No ClinGen
TOPMed
gnomAD
CA410346404
rs1167003576
847 F>V No ClinGen
gnomAD
rs141120816
CA10038526
848 S>I No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038525
rs141120816
848 S>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA410346387
rs1335871032
849 D>V No ClinGen
TOPMed
rs1165385785
CA410346381
850 S>C No ClinGen
gnomAD
rs773821830
CA10038524
850 S>P No ClinGen
ExAC
gnomAD
CA410346374
rs1364964452
851 S>L No ClinGen
gnomAD
CA10038523
rs768240147
855 N>S No ClinGen
ExAC
gnomAD
rs1569101869
CA410346339
856 F>C No ClinGen
Ensembl
rs1184415473
CA410346342
856 F>V No ClinGen
gnomAD
rs1250074046
CA410346334
857 D>N No ClinGen
gnomAD
CA10038521
rs200682570
858 S>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1223893851
CA410346322
859 E>K No ClinGen
TOPMed
rs778181370
CA10038518
861 S>F No ClinGen
ExAC
gnomAD
rs758645801
CA10038517
862 S>C No ClinGen
ExAC
TOPMed
gnomAD
rs778937065
CA10038515
864 L>P No ClinGen
ExAC
gnomAD
rs753338432
CA10038513
866 E>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs756012825
CA10038511
869 S>I No ClinGen
ExAC
gnomAD
CA410346249
rs1460775662
870 L>I No ClinGen
gnomAD
CA410346232
rs1161370653
872 K>N No ClinGen
gnomAD
rs1415546282
CA410346235
872 K>R No ClinGen
gnomAD
CA10038510
rs750266261
873 Q>R No ClinGen
ExAC
TOPMed
gnomAD
rs1601630390
CA410346206
876 I>T No ClinGen
Ensembl
rs139516786
CA10038508
877 Q>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 880 E>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs762621198
CA10038506
881 E>D No ClinGen
ExAC
TOPMed
gnomAD
rs775112741
CA10038504
882 P>A No ClinGen
ExAC
gnomAD
rs199778808
CA321458094
COSM116415
885 E>A ovary [Cosmic] No ClinGen
cosmic curated
Ensembl
rs771618331
CA10038502
888 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs1297277667
CA410346119
889 E>Q No ClinGen
TOPMed
rs1396522820
CA410346112
890 A>T No ClinGen
TOPMed
rs372053446
CA10038500
891 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038501
rs747545877
891 P>S No ClinGen
ExAC
gnomAD
CA10038498
rs150969897
892 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA410346085
rs749409453
894 S>I No ClinGen
ExAC
gnomAD
CA10038495
rs749409453
894 S>N No ClinGen
ExAC
gnomAD
CA410346082
rs1322313076
895 T>A No ClinGen
TOPMed
gnomAD
rs1401147421
CA410346077
895 T>I No ClinGen
TOPMed
gnomAD
CA10038494
rs780085357
896 A>V No ClinGen
ExAC
gnomAD
CA410346070
rs1156841826
897 P>A No ClinGen
gnomAD
rs1226908869
CA410346066
897 P>L No ClinGen
TOPMed
CA10038493
rs756137647
898 K>R No ClinGen
ExAC
gnomAD
TCGA novel 899 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs934712862
CA321458005
900 A>T No ClinGen
Ensembl
rs375162411
CA10038491
900 A>V No ClinGen
ESP
ExAC
gnomAD
CA410346042
rs1250218835
901 G>A No ClinGen
TOPMed
gnomAD
CA410346043
rs1250218835
901 G>D No ClinGen
TOPMed
gnomAD
rs751296592
CA10038489
902 P>L No ClinGen
ExAC
gnomAD
CA10038488
rs763850795
903 S>G No ClinGen
ExAC
rs1601630023
CA410346030
903 S>R No ClinGen
Ensembl
CA10038487
rs762676052
906 A>G No ClinGen
ExAC
gnomAD
CA10038486
rs775237726
907 S>C No ClinGen
ExAC
gnomAD
CA10038485
rs372046037
907 S>R No ClinGen
ESP
ExAC
gnomAD
rs1268338291
CA410345998
908 L>P No ClinGen
TOPMed
CA410345981
rs1490648925
911 C>R No ClinGen
TOPMed
rs1233033090
CA410345973
912 E>K No ClinGen
TOPMed
gnomAD
CA410345858
rs1428309057
917 M>T No ClinGen
TOPMed
CA10038482
rs368359632
919 T>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1431227424
CA410345778
921 H>Y No ClinGen
TOPMed
gnomAD
rs1161108523
CA410345745
922 K>E No ClinGen
TOPMed
CA410345647
rs1325763816
926 R>C No ClinGen
gnomAD
CA321457932
rs762954242
COSM1030960
926 R>H Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
gnomAD
CA10038480
rs374211935
928 Q>R No ClinGen
ExAC
gnomAD
COSM1030959
CA321457930
rs947543260
929 E>D Variant assessed as Somatic; impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
CA321457923
rs921538877
930 L>F No ClinGen
TOPMed
gnomAD
TCGA novel 930 L>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10038478
rs749534177
933 S>A No ClinGen
ExAC
gnomAD
rs1601629760
TCGA novel
CA410345510
933 S>C Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
Ensembl
TCGA novel 938 I>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1569101340
CA410345394
939 C>S No ClinGen
Ensembl
CA321457889
rs112728032
940 H>R No ClinGen
Ensembl
rs745874227
CA10038474
941 V>M No ClinGen
ExAC
TOPMed
gnomAD
rs781245566
CA10038473
943 N>S No ClinGen
ExAC
gnomAD
rs751422900
CA10038471
947 R>C No ClinGen
ExAC
TOPMed
gnomAD
rs777737264
CA10038470
947 R>H No ClinGen
ExAC
gnomAD
CA410345216
rs1268329894
949 N>D No ClinGen
TOPMed
gnomAD
rs911512275
CA321457822
951 R>Q No ClinGen
Ensembl
CA321457804
rs936275478
956 F>I No ClinGen
TOPMed
CA10038467
rs764926439
958 S>L No ClinGen
ExAC
gnomAD
rs375385271
CA321457781
960 M>T No ClinGen
ESP
TOPMed
rs1372615388
CA410345063
960 M>V No ClinGen
gnomAD
rs768107216
CA10038463
961 S>F No ClinGen
ExAC
gnomAD
CA321457774
rs17855811
961 S>P No ClinGen
Ensembl
rs1187459808
CA410345039
962 Q>E No ClinGen
TOPMed
CA321457762
rs950487773
962 Q>R No ClinGen
TOPMed
CA410345024
rs1450911282
963 A>P No ClinGen
TOPMed
CA410345016
rs1410602030
963 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs762202196
CA10038462
966 E>A No ClinGen
ExAC
gnomAD
CA410344988
rs1384024418
966 E>K No ClinGen
TOPMed
CA10038461
rs774872553
967 S>L No ClinGen
ExAC
TOPMed
gnomAD
rs546838794
CA10038459
973 E>Q No ClinGen
1000Genomes
ExAC
gnomAD
rs767404797
CA10038457
975 C>F No ClinGen
ExAC
TOPMed
gnomAD
rs775700350
CA10038458
975 C>R No ClinGen
ExAC
gnomAD
rs767404797
CA410344875
975 C>Y No ClinGen
ExAC
TOPMed
gnomAD
CA10038456
rs746025143
976 P>R No ClinGen
ExAC
gnomAD
rs142917163
CA10038454
977 V>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10038455
rs773271632
977 V>F No ClinGen
ExAC
gnomAD
rs773271632
CA321457726
977 V>I No ClinGen
ExAC
gnomAD
CA10038452
rs140576114
978 P>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038453
rs140576114
978 P>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1555909996
CA10038450
979 T>A No ClinGen
Ensembl
CA410344837
rs1298835339
979 T>K No ClinGen
gnomAD
rs752527926
CA10038448
980 N>S No ClinGen
ExAC
gnomAD
CA10038449
rs752527926
980 N>T No ClinGen
ExAC
gnomAD
CA410344814
rs1353006124
981 S>C No ClinGen
gnomAD
rs1601629269
CA410344819
981 S>P No ClinGen
Ensembl
CA410344773
rs1390609419
985 P>S No ClinGen
TOPMed
CA10038445
rs144240028
986 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA321457676
rs144240028
986 P>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA410344739
rs1473930722
988 P>Q No ClinGen
gnomAD
rs1159094214
CA410344745
988 P>S No ClinGen
TOPMed
gnomAD
CA321457655
rs1013212435
989 P>L No ClinGen
TOPMed
rs950567077
CA321457644
990 P>A No ClinGen
TOPMed
CA410344708
rs1569100914
990 P>R No ClinGen
Ensembl
CA410344698
rs765828457
991 P>A No ClinGen
ExAC
TOPMed
rs765828457
CA10038443
991 P>S No ClinGen
ExAC
TOPMed
rs764523483
CA10038438
995 K>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1601629028
CA410344592
996 I>T No ClinGen
Ensembl
TCGA novel 997 Q>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410344557
rs763362990
999 L>V No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 1000 E>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs770052989
CA10038435
1001 P>A No ClinGen
ExAC
gnomAD
CA10038434
rs759702653
1004 P>L No ClinGen
ExAC
gnomAD
rs1307740872
CA410344422
1005 T>A No ClinGen
gnomAD
rs770924280
CA10038432
1006 G>D No ClinGen
ExAC
gnomAD
CA10038433
rs776875600
1006 G>S No ClinGen
ExAC
TOPMed
gnomAD
CA10038431
rs747052597
1007 L>P No ClinGen
ExAC
gnomAD
rs1455743977
CA410344365
1009 E>K No ClinGen
TOPMed
gnomAD
rs778826027
CA321457590
1010 N>S No ClinGen
ExAC
gnomAD
rs778826027
CA10038427
1010 N>T No ClinGen
ExAC
gnomAD
rs373779800
CA10038426
1011 P>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs142014954
CA10038423
1012 T>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10038422
rs749920367
1012 T>I No ClinGen
ExAC
TOPMed
gnomAD
rs142014954
CA10038424
1012 T>P No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs142014954
CA10038425
1012 T>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs758869396
CA10038420
1013 P>A No ClinGen
ExAC
rs758869396
CA10038419
1013 P>S No ClinGen
ExAC
rs200489904
CA10038417
1014 A>P No ClinGen
1000Genomes
ExAC
gnomAD
rs1215115542
CA410344100
1023 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs1215115542
CA410344097
1023 E>Q No ClinGen
TOPMed
gnomAD
CA410344055
rs1282724056
1025 D>G No ClinGen
gnomAD
rs562308514
CA410344029
1026 T>I No ClinGen
1000Genomes
ExAC
gnomAD
CA10038413
rs562308514
1026 T>S No ClinGen
1000Genomes
ExAC
gnomAD
TCGA novel 1027 L>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10038410
rs765937096
1027 L>V No ClinGen
ExAC
gnomAD
rs1363235634 1029 Y>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No NCI-TCGA
CA10038407
rs774387444
1031 A>G No ClinGen
ExAC
gnomAD
CA10038408
rs748116197
1031 A>S No ClinGen
ExAC
gnomAD
rs1442615054
CA410343946
1032 P>A No ClinGen
TOPMed
CA10038406
rs370559494
1035 S>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA321457491
rs769996089
1036 A>V No ClinGen
Ensembl
TCGA novel 1036 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA410343890
rs1173665121
1037 I>V No ClinGen
TOPMed
gnomAD
rs779631015
CA10038404
1038 T>R No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 1041 R>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs745420430
CA10038401
1044 M>I No ClinGen
ExAC
TOPMed
gnomAD
rs1347403189
CA410343743
1047 L>F No ClinGen
gnomAD
rs1569100351
CA410343738
1047 L>R No ClinGen
Ensembl
rs1347403189
CA410343744
1047 L>V No ClinGen
gnomAD
CA410343667
rs1230065350
1052 F>L No ClinGen
gnomAD
rs1308507840
CA410343646
1054 T>S No ClinGen
gnomAD
CA10038398
rs753207923
1057 S>G No ClinGen
ExAC
gnomAD
CA410343596
rs1213261502
1058 L>F No ClinGen
TOPMed
gnomAD
CA321457449
rs201673550
1059 W>R No ClinGen
Ensembl
CA321457431
rs145089510
1066 N>D No ClinGen
ESP
TOPMed
gnomAD
CA10038394
rs766552756
1066 N>K No ClinGen
ExAC
TOPMed
gnomAD
rs754229429
CA10038395
1066 N>S No ClinGen
ExAC
gnomAD

No associated diseases with Q9ULJ3

11 regional properties for Q9ULJ3

Type Name Position InterPro Accession
domain BTB/POZ domain 20 - 126 IPR000210
domain Zinc finger C2H2-type 546 - 574 IPR013087-1
domain Zinc finger C2H2-type 575 - 598 IPR013087-2
domain Zinc finger C2H2-type 670 - 697 IPR013087-3
domain Zinc finger C2H2-type 722 - 742 IPR013087-4
domain Zinc finger C2H2-type 748 - 768 IPR013087-5
domain Zinc finger C2H2-type 775 - 803 IPR013087-6
domain Zinc finger C2H2-type 909 - 936 IPR013087-7
domain Zinc finger C2H2-type 937 - 964 IPR013087-8
domain Zinc finger C2H2-type 1043 - 1066 IPR013087-9
domain ZBTB21, zinc finger domain 746 - 773 IPR041011

Functions

Description
EC Number
Subcellular Localization
  • Nucleus
  • Colocalizes with ZBTB14 in nucleus in HEK293 cells
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

3 GO annotations of cellular component

Name Definition
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
nucleoplasm That part of the nuclear content other than the chromosomes or the nucleolus.
nucleus A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent.

7 GO annotations of molecular function

Name Definition
DNA-binding transcription factor activity, RNA polymerase II-specific A DNA-binding transcription factor activity that modulates the transcription of specific gene sets transcribed by RNA polymerase II.
DNA-binding transcription repressor activity, RNA polymerase II-specific A DNA-binding transcription factor activity that represses or decreases the transcription of specific gene sets transcribed by RNA polymerase II.
identical protein binding Binding to an identical protein or proteins.
metal ion binding Binding to a metal ion.
methyl-CpG binding Binding to a methylated cytosine/guanine dinucleotide.
POZ domain binding Binding to a POZ (poxvirus and zinc finger) domain of a protein, a protein-protein interaction domain found in many transcription factors.
sequence-specific DNA binding Binding to DNA of a specific nucleotide composition, e.g. GC-rich DNA binding, or with a specific sequence motif or type of DNA e.g. promotor binding or rDNA binding.

3 GO annotations of biological process

Name Definition
negative regulation of DNA-templated transcription Any process that stops, prevents, or reduces the frequency, rate or extent of cellular DNA-templated transcription.
negative regulation of transcription by RNA polymerase II Any process that stops, prevents, or reduces the frequency, rate or extent of transcription mediated by RNA polymerase II.
regulation of transcription by RNA polymerase II Any process that modulates the frequency, rate or extent of transcription mediated by RNA polymerase II.

178 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q08DS3 OSR1 Protein odd-skipped-related 1 Bos taurus (Bovine) PR
Q2VWH6 FEZF2 Fez family zinc finger protein 2 Bos taurus (Bovine) PR
A6QNZ0 ZSCAN26 Zinc finger and SCAN domain-containing protein 26 Bos taurus (Bovine) PR
A7MBI1 ZFP69 Zinc finger protein 69 homolog Bos taurus (Bovine) PR
Q08705 CTCF Transcriptional repressor CTCF Gallus gallus (Chicken) PR
O42409 GFI1B Zinc finger protein Gfi-1b Gallus gallus (Chicken) PR
A2T6W2 ZNF449 Zinc finger protein 449 Pan troglodytes (Chimpanzee) PR
Q9U405 grau Transcription factor grauzone Drosophila melanogaster (Fruit fly) PR
Q7K0S9 sug Zinc finger protein GLIS2 homolog Drosophila melanogaster (Fruit fly) PR
P20385 Cf2 Chorion transcription factor Cf2 Drosophila melanogaster (Fruit fly) PR
Q86P48 ATbp AT-rich binding protein Drosophila melanogaster (Fruit fly) PR
P28698 MZF1 Myeloid zinc finger 1 Homo sapiens (Human) PR
Q9NTW7 ZFP64 Zinc finger protein 64 Homo sapiens (Human) PR
O14978 ZNF263 Zinc finger protein 263 Homo sapiens (Human) PR
O60304 ZNF500 Zinc finger protein 500 Homo sapiens (Human) PR
P08151 GLI1 Zinc finger protein GLI1 Homo sapiens (Human) PR
P18146 EGR1 Early growth response protein 1 Homo sapiens (Human) PR
Q9Y5W3 KLF2 Krueppel-like factor 2 Homo sapiens (Human) PR
Q9UNY5 ZNF232 Zinc finger protein 232 Homo sapiens (Human) PR
Q96SZ4 ZSCAN10 Zinc finger and SCAN domain-containing protein 10 Homo sapiens (Human) PR
P17028 ZNF24 Zinc finger protein 24 Homo sapiens (Human) PR
P57682 KLF3 Krueppel-like factor 3 Homo sapiens (Human) PR
P25490 YY1 Transcriptional repressor protein YY1 Homo sapiens (Human) SS
O43296 ZNF264 Zinc finger protein 264 Homo sapiens (Human) PR
P49711 CTCF Transcriptional repressor CTCF Homo sapiens (Human) PR
Q9NQX1 PRDM5 PR domain zinc finger protein 5 Homo sapiens (Human) PR
Q9HBE1 PATZ1 POZ-, AT hook-, and zinc finger-containing protein 1 Homo sapiens (Human) PR
Q8TAX0 OSR1 Protein odd-skipped-related 1 Homo sapiens (Human) PR
Q9UL58 ZNF215 Zinc finger protein 215 Homo sapiens (Human) PR
Q8TBJ5 FEZF2 Fez family zinc finger protein 2 Homo sapiens (Human) PR
Q96SR6 ZNF382 Zinc finger protein 382 Homo sapiens (Human) PR
Q96IT1 ZNF496 Zinc finger protein 496 Homo sapiens (Human) PR
Q96N95 ZNF396 Zinc finger protein 396 Homo sapiens (Human) PR
O75840 KLF7 Krueppel-like factor 7 Homo sapiens (Human) PR
Q9H9D4 ZNF408 Zinc finger protein 408 Homo sapiens (Human) PR
Q13127 REST RE1-silencing transcription factor Homo sapiens (Human) PR
Q8IZM8 ZNF654 Zinc finger protein 654 Homo sapiens (Human) PR
P17022 ZNF18 Zinc finger protein 18 Homo sapiens (Human) PR
Q86XF7 ZNF575 Zinc finger protein 575 Homo sapiens (Human) PR
Q06889 EGR3 Early growth response protein 3 Homo sapiens (Human) PR
Q8NAM6 ZSCAN4 Zinc finger and SCAN domain-containing protein 4 Homo sapiens (Human) PR
Q08ER8 ZNF543 Zinc finger protein 543 Homo sapiens (Human) PR
P17029 ZKSCAN1 Zinc finger protein with KRAB and SCAN domains 1 Homo sapiens (Human) PR
Q8N680 ZBTB2 Zinc finger and BTB domain-containing protein 2 Homo sapiens (Human) PR
O95625 ZBTB11 Zinc finger and BTB domain-containing protein 11 Homo sapiens (Human) PR
Q9NPC7 MYNN Myoneurin Homo sapiens (Human) PR
Q96BV0 ZNF775 Zinc finger protein 775 Homo sapiens (Human) PR
Q8NF99 ZNF397 Zinc finger protein 397 Homo sapiens (Human) PR
Q63HK3 ZKSCAN2 Zinc finger protein with KRAB and SCAN domains 2 Homo sapiens (Human) PR
Q5FWF6 ZNF789 Zinc finger protein 789 Homo sapiens (Human) PR
Q15776 ZKSCAN8 Zinc finger protein with KRAB and SCAN domains 8 Homo sapiens (Human) PR
Q53GI3 ZNF394 Zinc finger protein 394 Homo sapiens (Human) PR
O95125 ZNF202 Zinc finger protein 202 Homo sapiens (Human) PR
Q05516 ZBTB16 Zinc finger and BTB domain-containing protein 16 Homo sapiens (Human) PR
Q9H116 GZF1 GDNF-inducible zinc finger protein 1 Homo sapiens (Human) PR
Q8N0Y2 ZNF444 Zinc finger protein 444 Homo sapiens (Human) PR
Q6P9G9 ZNF449 Zinc finger protein 449 Homo sapiens (Human) PR
Q8IW36 ZNF695 Zinc finger protein 695 Homo sapiens (Human) PR
Q5VTD9 GFI1B Zinc finger protein Gfi-1b Homo sapiens (Human) PR
Q6PG37 ZNF790 Zinc finger protein 790 Homo sapiens (Human) PR
Q9NQV6 PRDM10 PR domain zinc finger protein 10 Homo sapiens (Human) PR
Q9Y4E5 ZNF451 E3 SUMO-protein ligase ZNF451 Homo sapiens (Human) PR
Q8ND82 ZNF280C Zinc finger protein 280C Homo sapiens (Human) PR
Q49AA0 ZFP69 Zinc finger protein 69 homolog Homo sapiens (Human) PR
O43298 ZBTB43 Zinc finger and BTB domain-containing protein 43 Homo sapiens (Human) PR
Q9Y330 ZBTB12 Zinc finger and BTB domain-containing protein 12 Homo sapiens (Human) PR
Q13105 ZBTB17 Zinc finger and BTB domain-containing protein 17 Homo sapiens (Human) PR
P51508 ZNF81 Zinc finger protein 81 Homo sapiens (Human) PR
Q5JNZ3 ZNF311 Zinc finger protein 311 Homo sapiens (Human) PR
Q9BRR0 ZKSCAN3 Zinc finger protein with KRAB and SCAN domains 3 Homo sapiens (Human) PR
Q969J2 ZKSCAN4 Zinc finger protein with KRAB and SCAN domains 4 Homo sapiens (Human) PR
P49910 ZNF165 Zinc finger protein 165 Homo sapiens (Human) PR
Q9Y4X4 KLF12 Krueppel-like factor 12 Homo sapiens (Human) PR
P10074 ZBTB48 Telomere zinc finger-associated protein Homo sapiens (Human) PR
P17010 ZFX Zinc finger X-chromosomal protein Homo sapiens (Human) PR
Q9H5H4 ZNF768 Zinc finger protein 768 Homo sapiens (Human) PR
Q6NSZ9 ZSCAN25 Zinc finger and SCAN domain-containing protein 25 Homo sapiens (Human) PR
Q9Y2L8 ZKSCAN5 Zinc finger protein with KRAB and SCAN domains 5 Homo sapiens (Human) PR
Q86UZ6 ZBTB46 Zinc finger and BTB domain-containing protein 46 Homo sapiens (Human) PR
Q9NX65 ZSCAN32 Zinc finger and SCAN domain-containing protein 32 Homo sapiens (Human) PR
O14771 ZNF213 Zinc finger protein 213 Homo sapiens (Human) PR
Q8IWY8 ZSCAN29 Zinc finger and SCAN domain-containing protein 29 Homo sapiens (Human) PR
Q8NCP5 ZBTB44 Zinc finger and BTB domain-containing protein 44 Homo sapiens (Human) PR
P41182 BCL6 B-cell lymphoma 6 protein Homo sapiens (Human) PR
Q9NQX0 PRDM6 Putative histone-lysine N-methyltransferase PRDM6 Homo sapiens (Human) PR
Q9BU19 ZNF692 Zinc finger protein 692 Homo sapiens (Human) PR
Q08AG5 ZNF844 Zinc finger protein 844 Homo sapiens (Human) PR
Q6R2W3 ZBED9 SCAN domain-containing protein 3 Homo sapiens (Human) PR
P98182 ZNF200 Zinc finger protein 200 Homo sapiens (Human) PR
Q9UK11 ZNF223 Zinc finger protein 223 Homo sapiens (Human) PR
O15156 ZBTB7B Zinc finger and BTB domain-containing protein 7B Homo sapiens (Human) PR
Q6ZMS7 ZNF783 Zinc finger protein 783 Homo sapiens (Human) PR
P59923 ZNF445 Zinc finger protein 445 Homo sapiens (Human) PR
Q8N859 ZNF713 Zinc finger protein 713 Homo sapiens (Human) PR
Q99612 KLF6 Krueppel-like factor 6 Homo sapiens (Human) PR
Q8TD17 ZNF398 Zinc finger protein 398 Homo sapiens (Human) PR
P52739 ZNF131 Zinc finger protein 131 Homo sapiens (Human) PR
A6NGD5 ZSCAN5C Zinc finger and SCAN domain-containing protein 5C Homo sapiens (Human) PR
Q05215 EGR4 Early growth response protein 4 Homo sapiens (Human) PR
Q7Z398 ZNF550 Zinc finger protein 550 Homo sapiens (Human) PR
Q9Y2K1 ZBTB1 Zinc finger and BTB domain-containing protein 1 Homo sapiens (Human) PR
Q96N20 ZNF75A Zinc finger protein 75A Homo sapiens (Human) PR
A6NJL1 ZSCAN5B Zinc finger and SCAN domain-containing protein 5B Homo sapiens (Human) PR
A1YPR0 ZBTB7C Zinc finger and BTB domain-containing protein 7C Homo sapiens (Human) PR
Q9NWS9 ZNF446 Zinc finger protein 446 Homo sapiens (Human) PR
P24278 ZBTB25 Zinc finger and BTB domain-containing protein 25 Homo sapiens (Human) PR
Q96N38 ZNF714 Zinc finger protein 714 Homo sapiens (Human) PR
Q86YH2 ZNF280B Zinc finger protein 280B Homo sapiens (Human) PR
Q5TC79 ZBTB37 Zinc finger and BTB domain-containing protein 37 Homo sapiens (Human) PR
Q9UFB7 ZBTB47 Zinc finger and BTB domain-containing protein 47 Homo sapiens (Human) PR
Q14526 HIC1 Hypermethylated in cancer 1 protein Homo sapiens (Human) PR
Q9Y2D9 ZNF652 Zinc finger protein 652 Homo sapiens (Human) PR
O08584 Klf6 Krueppel-like factor 6 Mus musculus (Mouse) PR
Q61164 Ctcf Transcriptional repressor CTCF Mus musculus (Mouse) PR
Q810A1 Znf18 Zinc finger protein 18 Mus musculus (Mouse) PR
Q8BGS3 Zkscan1 Zinc finger protein with KRAB and SCAN domains 1 Mus musculus (Mouse) PR
Q00899 Yy1 Transcriptional repressor protein YY1 Mus musculus (Mouse) PR
P41183 Bcl6 B-cell lymphoma 6 protein homolog Mus musculus (Mouse) PR
Q9DAI4 Zbtb43 Zinc finger and BTB domain-containing protein 43 Mus musculus (Mouse) PR
O70237 Gfi1b Zinc finger protein Gfi-1b Mus musculus (Mouse) PR
Q99KZ6 Znf639 Zinc finger protein 639 Mus musculus (Mouse) PR
Q9Z1D9 Znf394 Zinc finger protein 394 Mus musculus (Mouse) PR
Q9CXE0 Prdm5 PR domain zinc finger protein 5 Mus musculus (Mouse) PR
P43300 Egr3 Early growth response protein 3 Mus musculus (Mouse) PR
Q9DAU9 Znf654 Zinc finger protein 654 Mus musculus (Mouse) PR
Q9R1Y5 Hic1 Hypermethylated in cancer 1 protein Mus musculus (Mouse) PR
Q8R0T2 Znf768 Zinc finger protein 768 Mus musculus (Mouse) PR
Q9WVG7 Osr1 Protein odd-skipped-related 1 Mus musculus (Mouse) PR
Q8BI73 Znf775 Zinc finger protein 775 Mus musculus (Mouse) PR
Q8VCZ7 Zbtb7c Zinc finger and BTB domain-containing protein 7C Mus musculus (Mouse) PR
Q91VN1 Znf24 Zinc finger protein 24 Mus musculus (Mouse) PR
Q9DB38 Znf580 Zinc finger protein 580 Mus musculus (Mouse) PR
A7KBS4 Zscan4d Zinc finger and SCAN domain containing protein 4D Mus musculus (Mouse) PR
Q91VW9 Zkscan3 Zinc finger protein with KRAB and SCAN domains 3 Mus musculus (Mouse) PR
P10925 Zfy1 Zinc finger Y-chromosomal protein 1 Mus musculus (Mouse) PR
P08046 Egr1 Early growth response protein 1 Mus musculus (Mouse) PR
Q3TTC2 Yy2 Transcription factor YY2 Mus musculus (Mouse) PR
Q3UTQ7 Prdm10 PR domain zinc finger protein 10 Mus musculus (Mouse) PR
Q6P3Y5 Znf280c Zinc finger protein 280C Mus musculus (Mouse) PR
Q9ERU3 Znf22 Zinc finger protein 22 Mus musculus (Mouse) PR
Q8VIG1 Rest RE1-silencing transcription factor Mus musculus (Mouse) PR
Q9Z1D8 Zkscan5 Zinc finger protein with KRAB and SCAN domains 5 Mus musculus (Mouse) PR
Q8BID6 Zbtb46 Zinc finger and BTB domain-containing protein 46 Mus musculus (Mouse) PR
P17012 Zfx Zinc finger X-chromosomal protein Mus musculus (Mouse) PR
Q9WUK6 Zbtb18 Zinc finger and BTB domain-containing protein 18 Mus musculus (Mouse) PR
O35738 Klf12 Krueppel-like factor 12 Mus musculus (Mouse) PR
B2RXC5 Znf382 Zinc finger protein 382 Mus musculus (Mouse) PR
O08900 Ikzf3 Zinc finger protein Aiolos Mus musculus (Mouse) PR
Q5DU09 Znf652 Zinc finger protein 652 Mus musculus (Mouse) PR
Q5RJ54 Zscan26 Zinc finger and SCAN domain-containing protein 26 Mus musculus (Mouse) PR
Q8BLM0 Klf8 Krueppel-like factor 8 Mus musculus (Mouse) PR
Q99JB0 Klf7 Krueppel-like factor 7 Mus musculus (Mouse) PR
Q8R0A2 Zbtb44 Zinc finger and BTB domain-containing protein 44 Mus musculus (Mouse) PR
P20662 Zfy2 Zinc finger Y-chromosomal protein 2 Mus musculus (Mouse) PR
Q80VJ6 Zscan4c Zinc finger and SCAN domain containing protein 4C Mus musculus (Mouse) PR
Q3URS2 Zscan4f Zinc finger and SCAN domain containing protein 4F Mus musculus (Mouse) PR
Q60980 Klf3 Krueppel-like factor 3 Mus musculus (Mouse) PR
Q8K3J5 Znf131 Zinc finger protein 131 Mus musculus (Mouse) PR
Q9Z2K3 Znf394 Zinc finger protein 394 Rattus norvegicus (Rat) PR
Q642B9 Znf18 Zinc finger protein 18 Rattus norvegicus (Rat) PR
B0K011 Osr1 Protein odd-skipped-related 1 Rattus norvegicus (Rat) PR
D3ZUU2 Gzf1 GDNF-inducible zinc finger protein 1 Rattus norvegicus (Rat) PR
B1WBU4 Zbtb8a Zinc finger and BTB domain-containing protein 8A Rattus norvegicus (Rat) PR
Q7TNK3 Znf24 Zinc finger protein 24 Rattus norvegicus (Rat) PR
O35819 Klf6 Krueppel-like factor 6 Rattus norvegicus (Rat) PR
Q9R1D1 Ctcf Transcriptional repressor CTCF Rattus norvegicus (Rat) PR
P43301 Egr3 Early growth response protein 3 Rattus norvegicus (Rat) PR
P08154 Egr1 Early growth response protein 1 Rattus norvegicus (Rat) PR
A0JPL0 Znf382 Zinc finger protein 382 Rattus norvegicus (Rat) PR
Q4KLI1 Zkscan1 Zinc finger protein with KRAB and SCAN domains 1 Rattus norvegicus (Rat) PR
A1L1J6 Znf652 Zinc finger protein 652 Rattus norvegicus (Rat) PR
Q9SHD0 ZAT4 Zinc finger protein ZAT4 Arabidopsis thaliana (Mouse-ear cress) PR
Q9LFU0 DOT3 BTB/POZ domain-containing protein DOT3 Arabidopsis thaliana (Mouse-ear cress) PR
Q0P4X6 zbtb44 Zinc finger and BTB domain-containing protein 44 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
A4II20 egr1 Early growth response protein 1 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q6P882 zbtb8a.2 Zinc finger and BTB domain-containing protein 8A.2 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q567C6 znf367 Zinc finger protein 367 Danio rerio (Zebrafish) (Brachydanio rerio) PR
A7Y7X5 znf711 Zinc finger protein 711 Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MEGLLHYINP AHAISLLSAL NEERLKGQLC DVLLIVGDQK FRAHKNVLAA SSEYFQSLFT
70 80 90 100 110 120
NKENESQTVF QLDFCEPDAF DNVLNYIYSS SLFVEKSSLA AVQELGYSLG ISFLTNIVSK
130 140 150 160 170 180
TPQAPFPTCP NRKKVFVEDD ENSSQKRSVI VCQSRNEAQG KTVSQNQPDV SHTSRPSPSI
190 200 210 220 230 240
AVKANTNKPH VPKPIEPLHN LSLTEKSWPK DSSVVYAKSL EHSGSLDDPN RISLVKRNAV
250 260 270 280 290 300
LPSKPLQDRE AMDDKPGVSG QLPKGKALEL ALKRPRPPVL SVCSSSETPY LLKETNKGNG
310 320 330 340 350 360
QGEDRNLLYY SKLGLVIPSS GSGSGNQSID RSGPLVKSLL RRSLSMDSQV PVYSPSIDLK
370 380 390 400 410 420
SSQGSSSVSS DAPGNVLCAL SQKSSLKDCS EKTALDDRPQ VLQPHRLRSF SASQSTDREG
430 440 450 460 470 480
ASPVTEVRIK TEPSSPLSDP SDIIRVTVGD AATTAAASSS SVTRDLSLKT EDDQKDMSRL
490 500 510 520 530 540
PAKRRFQADR RLPFKKLKVN EHGSPVSEDN FEEGSSPTLL DADFPDSDLN KDEFGELEGT
550 560 570 580 590 600
RPNKKFKCKH CLKIFRSTAG LHRHVNMYHN PEKPYACDIC HKRFHTNFKV WTHCQTQHGI
610 620 630 640 650 660
VKNPSPASSS HAVLDEKFQR KLIDIVRERE IKKALIIKLR RGKPGFQGQS SSQAQQVIKR
670 680 690 700 710 720
NLRSRAKGAY ICTYCGKAYR FLSQFKQHIK MHPGEKPLGV NKVAKPKEHA PLASPVENKE
730 740 750 760 770 780
VYQCRLCNAK LSSLLEQGSH ERLCRNAAVC PYCSLRFFSP ELKQEHESKC EYKKLTCLEC
790 800 810 820 830 840
MRTFKSSFSI WRHQVEVHNQ NNMAPTENFS LPVLDHNGDV TGSSRPQSQP EPNKVNHIVT
850 860 870 880 890 900
TKDDNVFSDS SEQVNFDSED SSCLPEDLSL SKQLKIQVKE EPVEEAEEEA PEASTAPKEA
910 920 930 940 950 960
GPSKEASLWP CEKCGKMFTV HKQLERHQEL LCSVKPFICH VCNKAFRTNF RLWSHFQSHM
970 980 990 1000 1010 1020
SQASEESAHK ESEVCPVPTN SPSPPPLPPP PPLPKIQPLE PDSPTGLSEN PTPATEKLFV
1030 1040 1050 1060
PQESDTLFYH APPLSAITFK RQFMCKLCHR TFKTAFSLWS HEQTHN