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

1 structures for Q63HK3

Entry ID Method Resolution Chain Position Source
AF-Q63HK3-F1 Predicted AlphaFoldDB

842 variants for Q63HK3

Variant ID(s) Position Change Description Diseaes Association Provenance
rs201538791
CA279663187
3 V>G No ClinGen
Ensembl
rs371195148
CA7972867
3 V>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395295761
rs1386908780
4 A>V No ClinGen
gnomAD
rs1423210207
CA395295754
5 L>P No ClinGen
gnomAD
CA395295748
rs767832318
6 D>A No ClinGen
ExAC
gnomAD
CA7972865
rs767832318
6 D>G No ClinGen
ExAC
gnomAD
TCGA novel 7 S>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972863
rs752024633
7 S>P No ClinGen
ExAC
gnomAD
rs752024633
CA7972864
7 S>T No ClinGen
ExAC
gnomAD
CA7972862
rs200532772
8 Q>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1322767994
CA395295729
9 I>S No ClinGen
TOPMed
gnomAD
CA395295723
rs1203354517
10 D>G No ClinGen
TOPMed
gnomAD
CA395295714
rs1456643755
11 A>V No ClinGen
gnomAD
rs1244456462
CA395295706
13 L>M No ClinGen
gnomAD
CA7972857
rs771945227
15 V>A No ClinGen
ExAC
gnomAD
CA7972856
rs771945227
15 V>D No ClinGen
ExAC
gnomAD
rs771945227
CA395295691
15 V>G No ClinGen
ExAC
gnomAD
rs1350631679
CA395295686
16 E>G No ClinGen
gnomAD
CA395295690
rs1229541953
16 E>K No ClinGen
gnomAD
CA395295667
rs1189713151
19 L>V No ClinGen
TOPMed
CA7972855
rs139400165
20 I>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972854
rs778927843
20 I>T No ClinGen
ExAC
gnomAD
CA395295653
rs1293922211
21 M>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs963862200
CA279663158
21 M>T No ClinGen
TOPMed
gnomAD
CA7972852
rs748885460
23 V>G No ClinGen
ExAC
TOPMed
gnomAD
rs770576000
CA7972853
23 V>M No ClinGen
ExAC
gnomAD
rs981629559
CA279663142
25 K>E No ClinGen
TOPMed
gnomAD
CA7972849
rs376019545
31 S>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972848
rs781555739
32 E>D No ClinGen
ExAC
gnomAD
rs755271057
CA7972847
34 I>F No ClinGen
ExAC
TOPMed
gnomAD
CA395295568
rs755271057
34 I>L No ClinGen
ExAC
TOPMed
gnomAD
CA7972846
rs752077333
37 G>R No ClinGen
ExAC
gnomAD
rs1299056587
CA395295540
38 S>W No ClinGen
TOPMed
TCGA novel 40 S>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA395295525
rs1328518250
40 S>I No ClinGen
TOPMed
rs1231573195
CA395295523
40 S>R No ClinGen
TOPMed
CA7972845
rs766932600
43 T>I No ClinGen
ExAC
gnomAD
CA395295492
rs1287191451
45 R>L No ClinGen
gnomAD
rs201842445
CA279663045
49 R>T No ClinGen
Ensembl
rs1385875203
CA395295439
52 C>S No ClinGen
gnomAD
rs1385875203
CA395295438
52 C>Y No ClinGen
gnomAD
rs368529222
CA395295428
53 Y>* No ClinGen
ESP
ExAC
TOPMed
CA7972838
rs201913124
54 E>D No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA395295423
rs1365301110
54 E>G No ClinGen
gnomAD
rs774274750
CA7972837
55 D>N No ClinGen
ExAC
gnomAD
rs1157049099
CA395295402
57 T>I No ClinGen
TOPMed
gnomAD
rs896086651
CA279662993
59 P>S No ClinGen
TOPMed
CA7972835
rs749145060
61 E>K No ClinGen
ExAC
gnomAD
rs1431629301
CA395295372
62 A>V No ClinGen
gnomAD
CA7972833
rs747844460
63 F>L No ClinGen
ExAC
TOPMed
gnomAD
CA7972834
rs772825288
63 F>V No ClinGen
ExAC
gnomAD
TCGA novel 64 S>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA279662902
rs957000061
64 S>T No ClinGen
Ensembl
rs199951945
CA7972830
65 K>N No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1266723003
CA395295347
66 L>F No ClinGen
gnomAD
rs780366560
CA7972828
72 R>L No ClinGen
ExAC
TOPMed
gnomAD
CA395295302
rs780366560
72 R>Q Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1567355449
CA395295275
76 P>L No ClinGen
Ensembl
CA7972827
rs376252162
78 M>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1567355443
CA395295241
81 K>T No ClinGen
Ensembl
rs1323300715
CA395295232
82 E>A No ClinGen
TOPMed
CA395295235
rs1385395959
82 E>Q No ClinGen
TOPMed
CA7972825
rs567096144
84 I>M No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1222689871
CA395295192
88 L>P No ClinGen
gnomAD
CA279662821
rs996380981
90 I>V No ClinGen
Ensembl
CA279662803
rs757215750
91 E>A No ClinGen
ExAC
TOPMed
gnomAD
CA7972824
rs757215750
91 E>G No ClinGen
ExAC
TOPMed
gnomAD
CA395295178
rs1225550975
91 E>K No ClinGen
TOPMed
TCGA novel 91 E>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972823
rs754124135
94 L>F No ClinGen
ExAC
gnomAD
CA7972822
rs764468680
95 T>A No ClinGen
ExAC
TOPMed
gnomAD
CA7972821
rs760973628
95 T>I No ClinGen
ExAC
TOPMed
gnomAD
rs774323991
CA7972820
100 K>E No ClinGen
ExAC
gnomAD
CA7972819
rs766061561
101 I>T No ClinGen
ExAC
rs762967904
CA7972818
103 A>T No ClinGen
ExAC
gnomAD
CA279662709
rs900711890
106 Q>R No ClinGen
TOPMed
gnomAD
rs143539580
CA7972815
107 K>N No ClinGen
ESP
ExAC
gnomAD
CA7972816
rs769362356
107 K>R No ClinGen
ExAC
gnomAD
CA7972817
rs769362356
107 K>T No ClinGen
ExAC
gnomAD
rs1567355402
CA395295062
108 Q>R No ClinGen
Ensembl
CA395295055
rs1490792977
109 C>Y No ClinGen
TOPMed
CA7972812
rs746643483
110 P>L No ClinGen
ExAC
gnomAD
rs746643483
CA395295047
110 P>R No ClinGen
ExAC
gnomAD
CA7972813
rs768341226
110 P>S No ClinGen
ExAC
gnomAD
CA395295043
rs1199351883
111 Q>R No ClinGen
gnomAD
rs780419562
CA7972811
112 S>N No ClinGen
ExAC
TOPMed
gnomAD
rs1228674068
CA395295031
113 G>R No ClinGen
gnomAD
rs1472596131
CA395295008
116 A>P No ClinGen
TOPMed
CA395295004
rs1385170947
116 A>V No ClinGen
TOPMed
gnomAD
rs746389645
CA7972809
118 A>S No ClinGen
ExAC
gnomAD
rs371020193
CA279662682
118 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ESP
NCI-TCGA
rs1597648763
CA395294985
120 V>G No ClinGen
Ensembl
rs779228119
CA7972808
121 V>A No ClinGen
ExAC
gnomAD
rs1163235125
CA395294973
122 H>R No ClinGen
TOPMed
TCGA novel 122 H>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972806
rs754038117
124 E>V No ClinGen
ExAC
gnomAD
TCGA novel 125 K>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972804
rs143433902
126 E>D No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1407176576
CA395294946
126 E>Q No ClinGen
TOPMed
rs1388760463
CA395294935
127 T>I No ClinGen
TOPMed
gnomAD
CA395294936
rs1388760463
127 T>S No ClinGen
TOPMed
gnomAD
rs766224298
CA7972802
128 G>E No ClinGen
ExAC
gnomAD
CA395294929
rs1368353019
129 R>G No ClinGen
gnomAD
rs1186228883
CA395294926
129 R>K No ClinGen
gnomAD
rs1166607810
CA395294913
131 R>I No ClinGen
TOPMed
gnomAD
rs1484441806
CA395294907
132 Q>L No ClinGen
gnomAD
CA7972800
rs750222002
133 Q>K No ClinGen
ExAC
gnomAD
rs1277399876
CA395294870
135 S>R No ClinGen
gnomAD
rs760122199
CA7972777
137 P>L No ClinGen
ExAC
TOPMed
gnomAD
rs370532156
CA7972776
138 V>M No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA279661432
rs148836306
140 R>P No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972774
rs148836306
140 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972775
rs771688659
140 R>W No ClinGen
ExAC
TOPMed
gnomAD
CA395294841
rs1456185714
141 E>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA7972772
rs771368883
143 H>P No ClinGen
ExAC
TOPMed
gnomAD
CA7972771
rs768530095
143 H>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1347156684
CA395294823
143 H>Y No ClinGen
gnomAD
rs1191473272
CA395294815
144 S>F No ClinGen
gnomAD
rs770414251
CA7972769
144 S>T No ClinGen
ExAC
gnomAD
rs538720527
CA7972768
146 L>V No ClinGen
ExAC
TOPMed
gnomAD
CA7972767
rs781305628
147 G>A Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1208193978
CA395294798
148 A>T No ClinGen
gnomAD
CA395294793
rs1315259352
148 A>V No ClinGen
gnomAD
rs755207927
CA7972766
149 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA7972765
rs377236803
149 A>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1597647860
CA395294772
151 E>D No ClinGen
Ensembl
rs116148718
CA7972762
152 V>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs571004941
CA279661383
152 V>L No ClinGen
gnomAD
CA7972761
rs764075345
153 A>V No ClinGen
ExAC
gnomAD
rs150169460
CA7972760
154 D>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs767031341
CA7972759
155 F>L No ClinGen
ExAC
gnomAD
CA7972758
rs767031341
155 F>V No ClinGen
ExAC
gnomAD
rs1342979226
CA395294747
156 Q>* No ClinGen
gnomAD
rs1177571113
CA395294746
156 Q>R No ClinGen
gnomAD
CA395294734
COSM389172
rs1199122648
158 E>Q lung [Cosmic] No ClinGen
cosmic curated
gnomAD
CA395294725
rs1423971678
159 Q>* No ClinGen
gnomAD
CA395294723
rs1171542596
159 Q>R No ClinGen
TOPMed
gnomAD
rs1567354888
CA395294704
162 T>A No ClinGen
Ensembl
CA395294686
rs1249179705
164 P>L No ClinGen
gnomAD
CA7972753
rs201820034
165 R>S No ClinGen
ExAC
TOPMed
gnomAD
rs748972478
CA7972755
165 R>W No ClinGen
ExAC
gnomAD
COSM969159
CA7972752
rs140961331
166 A>V endometrium [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs1210841698
CA395294665
168 S>C No ClinGen
gnomAD
CA395294663
rs776600069
169 R>G No ClinGen
ExAC
TOPMed
gnomAD
CA395294661
COSM471540
rs779774087
169 R>L kidney [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
rs779774087
CA7972749
169 R>Q No ClinGen
ExAC
TOPMed
gnomAD
CA7972750
rs776600069
169 R>W No ClinGen
ExAC
TOPMed
gnomAD
rs769395523
CA279661309
170 E>K No ClinGen
Ensembl
CA279661296
rs747201915
171 E>D No ClinGen
ExAC
TOPMed
gnomAD
CA395294637
rs1597647772
173 G>E No ClinGen
Ensembl
rs1352195139
CA395294640
173 G>R No ClinGen
TOPMed
CA7972746
rs534092020
176 H>L No ClinGen
1000Genomes
ExAC
gnomAD
rs534092020
CA7972745
176 H>P No ClinGen
1000Genomes
ExAC
gnomAD
rs758581080
CA279661290
177 S>T No ClinGen
Ensembl
CA395294603
rs1304102539
179 H>N No ClinGen
TOPMed
gnomAD
rs752627095
CA7972742
181 E>K No ClinGen
ExAC
gnomAD
rs766964408
CA7972741
182 Q>* No ClinGen
ExAC
gnomAD
rs956739704
CA279661229
184 N>S No ClinGen
TOPMed
gnomAD
rs1567354833
CA395294560
185 R>* No ClinGen
Ensembl
rs371976843
CA7972740
185 R>Q No ClinGen
ESP
ExAC
gnomAD
rs201521475
CA279661200
186 K>N No ClinGen
1000Genomes
TOPMed
gnomAD
rs1167684631
CA395294549
187 R>* No ClinGen
TOPMed
gnomAD
CA395294547
rs1426684240
187 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs751182407
COSM969158
CA7972739
189 R>C Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
rs113273135
CA7972738
189 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972737
rs113273135
189 R>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972735
rs765652025
190 R>Q No ClinGen
ExAC
TOPMed
gnomAD
CA7972736
rs188902981
190 R>W No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1483488660
CA395294508
194 K>R No ClinGen
gnomAD
rs531783165
CA7972716
197 R>Q No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs762180503
CA7972717
197 R>W No ClinGen
ExAC
rs1597646447
CA395294470
198 P>L No ClinGen
Ensembl
CA395294466
rs775594356
COSM434977
199 S>F Variant assessed as Somatic; impact. breast [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs761053407
CA7972714
199 S>P No ClinGen
ExAC
gnomAD
rs775594356
CA7972713
199 S>Y No ClinGen
ExAC
TOPMed
gnomAD
rs772090808
CA7972712
201 W>C No ClinGen
ExAC
gnomAD
rs1369522563
CA395294446
202 V>G No ClinGen
gnomAD
rs1293868979
CA395294439
204 A>T No ClinGen
gnomAD
CA7972711
rs367736337
205 L>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395294414
rs1161479729
208 E>K No ClinGen
gnomAD
rs1012899397
CA279659087
209 W>R No ClinGen
Ensembl
rs769487211
CA395294397
210 N>D No ClinGen
ExAC
gnomAD
TCGA novel 210 N>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs769487211
CA7972709
210 N>Y No ClinGen
ExAC
gnomAD
CA395294349
rs1159318834
217 T>P No ClinGen
TOPMed
CA395294343
rs1409261093
218 T>A No ClinGen
gnomAD
CA7972708
rs183473588
218 T>S No ClinGen
1000Genomes
ExAC
CA7972705
rs746898043
COSM702871
220 R>Q lung [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
rs768691519
CA7972707
220 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA395294317
rs757915595
223 A>P No ClinGen
ExAC
TOPMed
gnomAD
rs757915595
CA7972703
223 A>S No ClinGen
ExAC
TOPMed
gnomAD
CA395294308
rs1250373828
224 G>V No ClinGen
TOPMed
gnomAD
rs1442799185
CA395294302
225 S>F No ClinGen
TOPMed
rs1464815250
CA395294274
227 E>D No ClinGen
TOPMed
gnomAD
rs571530241
CA7972685
228 P>S No ClinGen
1000Genomes
ExAC
gnomAD
CA395294237
rs1202185748
233 H>L No ClinGen
gnomAD
CA395294233
rs200631425
233 H>Q No ClinGen
ESP
ExAC
gnomAD
rs374243689
CA279658290
234 V>M No ClinGen
ESP
TOPMed
gnomAD
CA7972683
rs143661348
235 A>D No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1051066580
CA279658274
236 R>G No ClinGen
TOPMed
gnomAD
TCGA novel 236 R>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs199548433
CA279658273
238 F>S No ClinGen
gnomAD
CA395294198
rs1454824462
239 S>F No ClinGen
TOPMed
CA7972682
rs745440078
240 Y>C No ClinGen
ExAC
gnomAD
CA7972681
rs778258437
242 K>R No ClinGen
ExAC
gnomAD
rs185234191
CA7972680
243 S>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs538166803
CA7972679
244 V>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA395294169
rs1325732773
244 V>M No ClinGen
gnomAD
CA395294158
rs778230521
245 H>Q No ClinGen
ExAC
gnomAD
rs547769682
CA279658251
247 I>F No ClinGen
Ensembl
CA7972677
rs756399282
247 I>M No ClinGen
ExAC
TOPMed
gnomAD
rs1334780891
CA395294138
248 P>L No ClinGen
gnomAD
rs568826414
CA7972676
249 A>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs2112811
CA7972675
VAR_033597
253 L>F No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs1324901953
CA395294103
254 Y>H No ClinGen
TOPMed
rs375897910
CA7972672
255 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972673
rs201469560
255 R>W No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972671
rs755342489
256 D>H No ClinGen
ExAC
gnomAD
rs755342489
CA7972670
256 D>N No ClinGen
ExAC
gnomAD
rs760605658
CA7972668
262 V>I No ClinGen
ExAC
gnomAD
rs775422144
CA395294030
264 N>K No ClinGen
ExAC
TOPMed
gnomAD
rs151071438
CA7972666
265 V>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972665
rs745776824
COSM1658890
266 V>F salivary_gland [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
CA395294014
rs1484469369
267 S>F No ClinGen
gnomAD
rs1410604263
CA395294012
268 L>V No ClinGen
gnomAD
CA279658148
rs868233963
269 G>* Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
rs762427083
CA7972644
269 G>E No ClinGen
ExAC
TOPMed
gnomAD
CA279652298
rs922012959
270 S>N No ClinGen
TOPMed
rs375748621
CA395293717
271 A>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA279652295
rs772773910
271 A>S No ClinGen
ExAC
TOPMed
gnomAD
rs772773910
CA7972643
271 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA7972642
rs375748621
271 A>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1259666017
CA395293715
272 V>M No ClinGen
TOPMed
CA395293703
rs1163584084
274 T>A No ClinGen
TOPMed
gnomAD
rs1158836601
CA395293692
275 S>F No ClinGen
gnomAD
rs763789877
CA7972640
275 S>R No ClinGen
ExAC
gnomAD
rs756958366
CA7972639
276 N>H No ClinGen
ExAC
TCGA novel 276 N>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972637
rs186241681
278 I>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1200670023
CA395293669
279 T>A No ClinGen
gnomAD
CA7972636
rs780488131
279 T>N No ClinGen
ExAC
gnomAD
rs369935233
CA395293665
280 R>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972634
rs199626499
280 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972635
rs369935233
280 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972633
rs779116261
285 K>N No ClinGen
ExAC
TOPMed
gnomAD
CA7972630
rs767421332
288 W>* No ClinGen
ExAC
TOPMed
gnomAD
rs61742723
CA7972631
288 W>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA279652249
rs369759537
289 T>I No ClinGen
Ensembl
rs148509747
CA7972629
289 T>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs766292694
CA7972627
290 L>P No ClinGen
ExAC
gnomAD
rs751355674
CA7972628
290 L>V No ClinGen
ExAC
TOPMed
gnomAD
CA395293582
rs1318359842
293 H>R No ClinGen
TOPMed
gnomAD
rs1389293689
CA395293574
294 S>C No ClinGen
TOPMed
rs144813841
CA7972625
295 S>F No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA395293571
rs1399775124
295 S>P No ClinGen
TOPMed
gnomAD
CA395293566
rs1240647580
296 N>D No ClinGen
TOPMed
CA395293544
rs1321214229
299 S>R No ClinGen
gnomAD
TCGA novel 300 I>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972622
rs776208714
302 R>* No ClinGen
ExAC
gnomAD
rs138595438
CA7972621
302 R>Q No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7972620
rs572372469
303 S>T No ClinGen
1000Genomes
ExAC
gnomAD
rs376803326
CA279652158
304 N>S No ClinGen
ESP
TOPMed
gnomAD
CA7972617
COSM3387334
rs746340371
306 V>I pancreas [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
rs746340371
CA7972618
306 V>L No ClinGen
ExAC
TOPMed
gnomAD
CA7972616
rs779163047
307 K>Q No ClinGen
ExAC
gnomAD
rs947749969
CA279652152
308 E>K No ClinGen
gnomAD
rs1428443710
CA395293474
309 K>N No ClinGen
TOPMed
gnomAD
rs1383236292
CA395293464
311 V>A No ClinGen
TOPMed
TCGA novel 311 V>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972615
rs757336756
311 V>I No ClinGen
ExAC
TOPMed
gnomAD
CA395293467
rs757336756
311 V>L No ClinGen
ExAC
TOPMed
gnomAD
CA395293461
rs1443972637
312 H>D No ClinGen
TOPMed
rs1301662407
CA395293458
312 H>R No ClinGen
gnomAD
rs754122239
CA7972614
313 A>P No ClinGen
ExAC
gnomAD
rs1366492704
CA395293450
313 A>V No ClinGen
TOPMed
gnomAD
rs1476449323
CA395293445
314 I>T No ClinGen
gnomAD
rs1351387632
COSM1749512
CA395293447
314 I>V urinary_tract [Cosmic] No ClinGen
cosmic curated
TOPMed
CA395293419
rs1597643082
316 V>A No ClinGen
Ensembl
CA279652110
rs890365937
316 V>I No ClinGen
TOPMed
rs778194416
CA7972613
317 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA7972612
rs756355033
318 A>V No ClinGen
ExAC
gnomAD
rs558961917
CA7972610
320 S>N No ClinGen
1000Genomes
ExAC
gnomAD
TCGA novel 320 S>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs372123893
CA7972609
321 A>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395293353
rs1171483890
322 G>R No ClinGen
gnomAD
TCGA novel 324 T>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA395293295
rs1420074756
326 R>K No ClinGen
TOPMed
gnomAD
rs1567352391
CA395293280
327 E>A No ClinGen
Ensembl
CA279652104
rs764621026
332 G>C No ClinGen
Ensembl
rs141526402
CA7972606
335 D>E No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA395293119
rs1245840256
338 I>T No ClinGen
TOPMed
CA395293109
rs1316409832
339 A>S No ClinGen
TOPMed
rs776117830
CA7972605
341 V>L No ClinGen
ExAC
TOPMed
gnomAD
rs777212497
CA279652095
345 Y>F No ClinGen
Ensembl
rs1250901874
CA395292941
352 L>M No ClinGen
TOPMed
TCGA novel 352 L>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA279652075
rs61746638
353 A>G No ClinGen
Ensembl
CA7972603
rs201142510
354 I>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1483077425
CA395292897
356 K>E No ClinGen
TOPMed
CA395292893
rs1483077425
356 K>Q No ClinGen
TOPMed
CA7972602
rs61746579
356 K>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972601
rs775742455
357 E>Q No ClinGen
ExAC
TOPMed
gnomAD
CA7972600
rs772439377
359 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA279652046
rs1022421687
359 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA7972599
rs746378839
363 T>A No ClinGen
ExAC
gnomAD
rs1415055762
CA395292815
364 L>R No ClinGen
gnomAD
rs1426450315
CA395292802
366 A>S No ClinGen
TOPMed
rs1354379366
CA395292784
369 R>* Variant assessed as Somatic; 4.62e-05 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs774937230
CA7972597
369 R>Q No ClinGen
ExAC
gnomAD
CA7972596
rs138008866
371 S>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395292765
rs1466891528
371 S>R No ClinGen
TOPMed
rs749445830
CA7972595
372 Q>E No ClinGen
ExAC
gnomAD
CA7972594
rs777968369
373 V>L No ClinGen
ExAC
gnomAD
CA395292736
rs777968369
373 V>M No ClinGen
ExAC
gnomAD
CA395292722
rs1416090766
374 Y>C No ClinGen
gnomAD
rs536523496
CA7972593
379 E>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA395292670
rs1452803702
379 E>K No ClinGen
TOPMed
CA7972592
rs748351738
382 R>Q No ClinGen
ExAC
gnomAD
rs1481198951
CA395292606
383 E>D No ClinGen
gnomAD
TCGA novel 383 E>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA279651998
rs954052974
384 C>R No ClinGen
Ensembl
rs1213115004
CA395292575
386 F>L No ClinGen
TOPMed
CA7972589
rs750206818
387 L>R No ClinGen
ExAC
gnomAD
CA7972587
rs757159120
391 E>G No ClinGen
ExAC
gnomAD
rs1295331620
CA395292513
391 E>K No ClinGen
TOPMed
CA395292499
rs1308493062
392 Q>* No ClinGen
TOPMed
rs753398621
CA7972586
394 R>* Variant assessed as Somatic; 0.0001386 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7972585
rs150756150
394 R>Q No ClinGen
ESP
ExAC
gnomAD
rs868584723
CA279651968
395 T>I No ClinGen
Ensembl
TCGA novel 401 Q>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1373831145
CA395292350
403 S>R No ClinGen
gnomAD
CA7972582
rs767784122
COSM294970
404 Y>C Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1460927614
CA395292347
404 Y>D No ClinGen
TOPMed
CA395292341
rs1439961923
COSM183907
405 R>* Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
CA7972581
rs760033233
405 R>Q No ClinGen
ExAC
gnomAD
CA7972580
rs774847431
408 R>K No ClinGen
ExAC
gnomAD
CA7972579
rs771605936
409 N>T No ClinGen
ExAC
TOPMed
gnomAD
CA7972576
rs148194807
CA395292291
412 M>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972577
rs773185486
412 M>V No ClinGen
ExAC
TOPMed
gnomAD
CA7972575
rs748332653
413 L>P No ClinGen
ExAC
gnomAD
rs1254105520
CA395292282
414 E>G No ClinGen
gnomAD
rs781534931
CA7972574
415 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA7972573
rs755189025
416 C>S No ClinGen
ExAC
gnomAD
CA395292265
rs141132571
417 A>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972571
rs141132571
417 A>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395292254
rs1221787243
418 F>L No ClinGen
gnomAD
rs1306039726
CA395292257
418 F>S No ClinGen
gnomAD
rs1317088313
CA395292259
418 F>V No ClinGen
gnomAD
CA395292246
rs1469805056
419 F>L No ClinGen
TOPMed
rs753737349
CA7972569
422 M>I No ClinGen
ExAC
gnomAD
CA395292229
rs1440054330
422 M>V No ClinGen
TOPMed
gnomAD
CA395292220
rs1290669425
423 D>H No ClinGen
TOPMed
gnomAD
rs755589722
CA7972567
425 L>F No ClinGen
ExAC
gnomAD
CA395292206
rs1157383329
425 L>V No ClinGen
TOPMed
gnomAD
rs1396043667
CA395292198
426 L>W No ClinGen
gnomAD
CA7972565
rs767264303
427 N>K No ClinGen
ExAC
gnomAD
CA7972564
rs759231746
COSM969155
431 R>C Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA7972562
rs143300766
431 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs143300766
CA7972563
431 R>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1259850847
CA395292164
432 A>S No ClinGen
gnomAD
rs763585057
CA7972561
433 P>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
TCGA novel 435 T>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972559
rs770190485
436 D>E No ClinGen
ExAC
TOPMed
gnomAD
CA279651816
rs1048820360
436 D>G No ClinGen
Ensembl
CA395292126
rs1233518471
438 P>Q No ClinGen
gnomAD
TCGA novel 441 M>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA395292103
rs1297838631
441 M>T No ClinGen
gnomAD
rs1481970199
CA395292106
441 M>V No ClinGen
TOPMed
gnomAD
CA7972557
rs776542820
442 I>T No ClinGen
ExAC
gnomAD
CA395292091
rs1384346980
443 P>A No ClinGen
gnomAD
CA395292076
rs1436779752
445 P>R No ClinGen
gnomAD
rs778713893
CA7972555
446 R>I No ClinGen
ExAC
TOPMed
gnomAD
rs778713893
CA7972554
446 R>T No ClinGen
ExAC
TOPMed
gnomAD
rs1214957280
CA395292069
447 L>M No ClinGen
TOPMed
CA395292066
rs1173348293
447 L>P No ClinGen
gnomAD
CA279651769
rs1015033012
450 I>T No ClinGen
TOPMed
gnomAD
CA7972553
rs373941531
451 A>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1392497299
CA395292043
451 A>S Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs373941531
CA395292039
451 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7972551
rs368887634
452 I>M No ClinGen
ExAC
TOPMed
gnomAD
rs1184448617
CA395292031
453 S>G No ClinGen
gnomAD
rs1275959581
CA395292029
453 S>N No ClinGen
gnomAD
rs201935635
CA7972550
454 A>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7972549
rs752287717
455 K>E No ClinGen
ExAC
TOPMed
gnomAD
CA395292019
rs752287717
455 K>Q No ClinGen
ExAC
TOPMed
gnomAD
CA7972548
rs780545200
457 H>R No ClinGen
ExAC
TOPMed
gnomAD
rs551448101
CA7972545
458 I>M No ClinGen
1000Genomes
ExAC
gnomAD
rs544630865
CA7972546
458 I>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs754700341
CA7972547
458 I>V No ClinGen
ExAC
gnomAD
rs750750284
CA7972543
459 S>N No ClinGen
ExAC
gnomAD
CA395291988
rs1293467870
459 S>R No ClinGen
TOPMed
gnomAD
rs750750284
CA7972544
459 S>T No ClinGen
ExAC
gnomAD
CA395291979
CA7972542
rs765813907
461 V>L No ClinGen
ExAC
gnomAD
rs1567352120
CA395291971
462 E>G No ClinGen
Ensembl
rs1567352120
CA395291972
462 E>V No ClinGen
Ensembl
CA7972540
rs762208179
463 E>V No ClinGen
ExAC
gnomAD
CA395291947
rs1312656118
465 E>V No ClinGen
gnomAD
rs1301707220
CA395291940
466 A>G No ClinGen
TOPMed
rs1323714206
CA395291943
466 A>T No ClinGen
gnomAD
rs768685041
CA7972539
467 A>E No ClinGen
ExAC
TOPMed
gnomAD
CA395291938
rs1345076886
467 A>T No ClinGen
TOPMed
CA7972538
rs768685041
467 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA7972537
rs760894861
468 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs1284836974
CA395291926
469 D>Y Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs140368025
CA279651604
470 S>Y No ClinGen
ESP
COSM1376957
rs996016910
CA279651599
471 D>G large_intestine [Cosmic] No ClinGen
cosmic curated
TOPMed
CA7972535
rs772266628
472 D>G No ClinGen
ExAC
gnomAD
rs777396575
CA7972534
473 D>E No ClinGen
ExAC
gnomAD
CA395291873
rs1167859606
476 G>V No ClinGen
gnomAD
rs149172025
CA395291866
477 I>M No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs78714728
CA7972531
478 E>K No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA395291841
rs1350305139
481 R>C No ClinGen
TOPMed
gnomAD
rs145224473
CA7972530
481 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972529
rs754469759
482 K>R No ClinGen
ExAC
gnomAD
rs954125144
CA279651569
483 S>A No ClinGen
Ensembl
CA395291817
rs1309136792
485 I>V No ClinGen
gnomAD
rs1196336047
CA395291810
486 H>N No ClinGen
gnomAD
CA7972528
rs375607715
486 H>R No ClinGen
ESP
ExAC
gnomAD
CA395291801
rs1445074635
487 G>D No ClinGen
TOPMed
gnomAD
CA395291803
rs1249699886
487 G>S No ClinGen
gnomAD
rs150009750
CA7972527
488 A>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1000931338
CA279651553
489 P>S No ClinGen
TOPMed
CA7972526
rs145658902
492 F>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1597642585
CA395291761
493 Q>H No ClinGen
Ensembl
CA395291754
rs11649280
CA395291753
494 N>K No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs961391486
CA279651536
495 L>F No ClinGen
TOPMed
rs961391486
CA395291751
495 L>V No ClinGen
TOPMed
CA395291745
rs1406375620
496 S>C No ClinGen
TOPMed
TCGA novel 497 G>= Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972508
rs267604478
498 V>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395291313
rs1176574935
500 W>* No ClinGen
TOPMed
rs1363046912
CA395291280
502 Y>C No ClinGen
TOPMed
CA395291224
rs1453974621
506 K>E No ClinGen
TOPMed
CA395291180
rs1567351474
508 F>S No ClinGen
Ensembl
rs75048235
CA279649566
509 L>P No ClinGen
Ensembl
CA7972504
rs757509119
513 R>C No ClinGen
ExAC
TOPMed
gnomAD
CA7972503
rs377678835
513 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 514 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs61744407
CA7972502
515 T>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs370863799
CA7972500
516 R>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972501
rs544572365
516 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7972499
rs767445128
520 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA395290968
rs1349049647
523 A>G No ClinGen
gnomAD
CA7972493
rs768764112
526 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs372737772
CA7972494
526 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972490
rs11642611
527 K>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs775174500
CA7972491
527 K>T No ClinGen
ExAC
gnomAD
CA7972488
rs778491540
528 S>C No ClinGen
ExAC
gnomAD
CA7972487
rs200508217
528 S>I No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs116889865
CA7972486
528 S>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972484
rs370783262
530 L>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs145544553
CA7972485
530 L>S No ClinGen
ESP
ExAC
gnomAD
CA395290923
rs1366364698
531 Y>N No ClinGen
TOPMed
rs1165051074
CA395290909
533 A>T No ClinGen
TOPMed
CA279649415
rs868519819
533 A>V No ClinGen
Ensembl
rs1242757133
CA395290892
536 E>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA7972481
COSM460571
rs754954301
539 R>Q cervix Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7972480
rs751644314
541 C>R No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 541 C>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972479
rs766550853
COSM1233500
542 G>S large_intestine [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
CA395290847
rs1347602407
542 G>V No ClinGen
gnomAD
CA279649361
rs938894108
543 F>Y No ClinGen
TOPMed
CA395290832
rs1363503251
545 R>Q No ClinGen
gnomAD
CA7972477
rs753709533
545 R>W No ClinGen
ExAC
gnomAD
TCGA novel 547 P>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs772036573
CA7972473
551 R>* No ClinGen
ExAC
gnomAD
CA7972472
rs759031829
551 R>Q No ClinGen
ExAC
gnomAD
TCGA novel 552 T>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972471
rs773877242
555 K>R No ClinGen
ExAC
gnomAD
rs773877242
CA395290765
555 K>T No ClinGen
ExAC
gnomAD
rs531491662
CA279649279
556 S>R No ClinGen
Ensembl
CA395290753
rs1173928896
557 L>F No ClinGen
gnomAD
rs748887876
CA7972469
562 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs770075484
CA7972467
562 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs770075484
CA7972468
562 R>L No ClinGen
ExAC
gnomAD
CA7972466
rs748667250
563 K>E No ClinGen
ExAC
gnomAD
COSM1323625
CA395290708
rs1411468877
563 K>N ovary [Cosmic] No ClinGen
cosmic curated
gnomAD
CA7972465
rs781607090
563 K>R No ClinGen
ExAC
gnomAD
CA395290693
rs1567351339
566 N>H No ClinGen
Ensembl
CA279649244
rs947821248
568 H>Y No ClinGen
TOPMed
CA7972462
rs147540232
569 V>M No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs750609886
CA7972460
573 C>F No ClinGen
ExAC
gnomAD
rs1196666665
CA395290647
573 C>R No ClinGen
TOPMed
CA395290642
rs144470614
573 C>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs760609581
CA7972458
574 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA7972457
rs61746620
574 A>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395290625
rs1354629675
576 Y>C No ClinGen
TOPMed
gnomAD
CA395290628
rs1414998048
576 Y>H No ClinGen
gnomAD
CA395290624
rs1354629675
576 Y>S No ClinGen
TOPMed
gnomAD
CA395290620
rs1300828899
577 K>E No ClinGen
gnomAD
rs1188288976
CA395290590
580 D>H No ClinGen
TOPMed
CA395290488
rs544640469
586 R>P No ClinGen
ExAC
TOPMed
gnomAD
CA7972451
rs544640469
586 R>Q No ClinGen
ExAC
TOPMed
gnomAD
COSM1233501
CA395290493
rs1476558388
586 R>W large_intestine Variant assessed as Somatic; impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
CA7972450
rs769422879
588 S>F Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs748577396
CA7972449
589 A>G No ClinGen
ExAC
gnomAD
CA279649113
rs112785166
589 A>S No ClinGen
Ensembl
TCGA novel 589 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972448
rs138363498
590 P>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1300236482
CA395290423
591 S>F Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
TCGA novel 593 S>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA395290397
rs769066261
593 S>I No ClinGen
ExAC
gnomAD
CA7972447
rs769066261
593 S>N No ClinGen
ExAC
gnomAD
TCGA novel 593 S>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972446
rs747511930
594 T>I No ClinGen
ExAC
TOPMed
gnomAD
CA7972445
rs201508777
595 P>L No ClinGen
1000Genomes
ExAC
gnomAD
rs1414379604
CA395290351
596 E>V No ClinGen
TOPMed
rs771884544
CA7972444
597 E>D No ClinGen
ExAC
TOPMed
gnomAD
rs745934236
CA7972443
598 V>I No ClinGen
ExAC
gnomAD
CA395290287
rs1308038742
600 S>L Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
rs757518433
CA7972441
600 S>P No ClinGen
ExAC
TOPMed
gnomAD
rs1229572349
CA395290209
606 R>* No ClinGen
TOPMed
rs1597641037
CA395290207
606 R>K No ClinGen
Ensembl
rs988950462
CA395290185
607 G>A No ClinGen
TOPMed
CA279649081
rs913418159
607 G>R No ClinGen
TOPMed
gnomAD
rs988950462
CA279649068
607 G>V No ClinGen
TOPMed
CA7972439
rs767291214
608 G>C No ClinGen
ExAC
gnomAD
rs548103236
CA7972438
608 G>V No ClinGen
1000Genomes
ExAC
gnomAD
rs1006674837
CA279649040
609 I>V No ClinGen
TOPMed
rs765885053
CA7972435
611 V>F No ClinGen
ExAC
TOPMed
gnomAD
rs369024502
CA7972433
613 P>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs369024502
CA7972434
613 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395290100
rs1348290826
613 P>S No ClinGen
gnomAD
rs764919978
CA7972432
614 Q>R No ClinGen
ExAC
gnomAD
rs8059494
CA7972431
VAR_033598
615 E>D No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs1429602905
CA395290073
615 E>K No ClinGen
TOPMed
CA395290038
rs1177361888
617 T>K No ClinGen
gnomAD
rs568858340
CA395290030
618 G>C No ClinGen
gnomAD
rs568858340
CA279648993
618 G>S No ClinGen
gnomAD
CA279648987
rs1021716603
619 W>* No ClinGen
TOPMed
rs1393650192
CA395290018
619 W>R No ClinGen
TOPMed
CA395290006
rs1213698174
620 E>G No ClinGen
gnomAD
rs1377524053
CA395289539
624 T>I No ClinGen
TOPMed
CA7972428
rs370948693
626 Q>* No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395289504
rs370948693
626 Q>E No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 626 Q>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs776124376
CA7972427
627 E>V No ClinGen
ExAC
gnomAD
CA7972426
rs772706151
629 V>L No ClinGen
ExAC
rs377141133
CA279648978
630 I>M No ClinGen
ESP
TOPMed
gnomAD
rs779110093
CA7972424
634 C>F No ClinGen
ExAC
gnomAD
CA7972425
rs745989274
634 C>G No ClinGen
ExAC
gnomAD
CA7972421
rs780850171
636 E>G No ClinGen
ExAC
TOPMed
gnomAD
CA7972420
rs374102276
637 R>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs751296845
CA7972419
639 S>N No ClinGen
ExAC
TOPMed
gnomAD
rs199539113
CA7972417
640 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs749958997
CA7972416
641 E>K No ClinGen
ExAC
gnomAD
rs1425283583
CA395289092
643 I>T No ClinGen
TOPMed
gnomAD
rs761378390
CA7972414
643 I>V No ClinGen
ExAC
gnomAD
rs138128307
CA7972413
644 V>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs763643043
CA7972412
645 Q>R No ClinGen
ExAC
gnomAD
CA7972411
rs190936908
646 E>V No ClinGen
1000Genomes
ExAC
gnomAD
rs1186048862
CA395289035
648 E>G No ClinGen
gnomAD
CA395289011
rs1188733296
651 G>E No ClinGen
TOPMed
CA395289015
rs1232400956
651 G>R No ClinGen
gnomAD
CA395289005
rs1297749474
652 P>L No ClinGen
gnomAD
rs772751162
CA395289008
652 P>S No ClinGen
ExAC
gnomAD
rs772751162
CA7972409
652 P>T No ClinGen
ExAC
gnomAD
CA395289004
rs1383018561
653 P>T No ClinGen
gnomAD
TCGA novel 657 Q>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs891006801
CA279648800
659 P>A No ClinGen
Ensembl
rs1340033736
CA395288963
659 P>R No ClinGen
gnomAD
CA7972407
rs774601872
660 N>D No ClinGen
ExAC
TOPMed
gnomAD
CA395288961
rs774601872
660 N>H No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 661 D>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1465425933
CA395288236
662 F>C No ClinGen
TOPMed
CA395288188
rs763157758
665 G>A No ClinGen
ExAC
TOPMed
gnomAD
rs763157758
CA7972381
665 G>E No ClinGen
ExAC
TOPMed
gnomAD
CA7972382
rs373353040
665 G>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1029315649
CA279645857
667 S>G No ClinGen
gnomAD
CA395288154
rs1319692860
667 S>N No ClinGen
TOPMed
CA7972380
rs370059069
670 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1597639062
CA395288074
671 D>E No ClinGen
Ensembl
rs377065788
CA395288091
671 D>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs377065788
CA7972378
671 D>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972377
rs779830282
675 I>L No ClinGen
ExAC
gnomAD
rs140315480
CA279645804
675 I>T No ClinGen
ESP
TOPMed
rs745650819
CA7972375
677 Y>C No ClinGen
ExAC
gnomAD
rs1243144462
CA395287961
678 K>R No ClinGen
gnomAD
TCGA novel 679 D>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7972374
rs144166062
679 D>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs753440463
CA7972372
683 H>N No ClinGen
ExAC
gnomAD
CA7972371
rs562726254
684 R>S No ClinGen
1000Genomes
ExAC
gnomAD
rs755818686
CA7972370
686 L>S No ClinGen
ExAC
TOPMed
gnomAD
CA279645730
rs1004608927
687 I>M No ClinGen
Ensembl
CA7972369
rs542953652
687 I>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs140318360
CA7972368
688 E>G No ClinGen
1000Genomes
ExAC
gnomAD
CA7972366
rs751967517
689 K>E No ClinGen
ExAC
CA279645686
rs1048729898
689 K>N No ClinGen
TOPMed
rs1179207352
CA395287697
690 S>P No ClinGen
gnomAD
CA7972365
COSM969153
rs766949580
690 S>Y Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA7972364
rs763347455
691 K>E No ClinGen
ExAC
TOPMed
gnomAD
CA7972363
rs143690617
691 K>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972362
rs143690617
691 K>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395287642
rs1431317075
692 R>I No ClinGen
TOPMed
CA395287614
rs1289516707
693 V>A No ClinGen
gnomAD
rs1468956747
CA395287630
693 V>I No ClinGen
gnomAD
rs762037481
CA7972361
694 V>A No ClinGen
ExAC
gnomAD
CA279645649
rs370426284
697 S>T No ClinGen
Ensembl
CA7972359
COSM3402208
rs148950715
699 D>N Variant assessed as Somatic; 0.0 impact. central_nervous_system [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs113175046
CA7972358
699 D>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs773999282
CA7972357
700 P>S No ClinGen
ExAC
gnomAD
rs1442538292
CA395287390
703 Y>C No ClinGen
TOPMed
gnomAD
rs777337504
CA7972354
704 R>C No ClinGen
ExAC
TOPMed
gnomAD
rs777337504
CA7972355
704 R>G No ClinGen
ExAC
TOPMed
gnomAD
rs144615670
CA7972353
704 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1403196994
CA395287357
705 K>E No ClinGen
gnomAD
rs1386911547
CA395287317
706 R>S No ClinGen
TOPMed
gnomAD
CA395287324
rs1597638920
706 R>T No ClinGen
Ensembl
rs371532046
CA7972351
709 I>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395287219
rs1597638892
710 S>L No ClinGen
Ensembl
rs752018693
CA279645524
713 Q>P No ClinGen
ExAC
TOPMed
gnomAD
rs752018693
CA7972349
713 Q>R No ClinGen
ExAC
TOPMed
gnomAD
CA395287110
rs1478419669
714 W>C No ClinGen
gnomAD
rs915276851
CA279645511
715 E>K No ClinGen
TOPMed
CA7972348
rs766603737
716 N>D No ClinGen
ExAC
gnomAD
TCGA novel 717 L>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1263933857
CA395287059
717 L>V No ClinGen
TOPMed
rs886134557
CA279645492
718 Q>* No ClinGen
TOPMed
rs1223296113
CA395287022
718 Q>R No ClinGen
TOPMed
CA395286985
rs1271214955
COSM3817624
719 G>E Variant assessed as Somatic; impact. breast [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
TCGA novel 721 R>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs750838403
CA7972346
722 Q>K No ClinGen
ExAC
TOPMed
gnomAD
rs201513889
CA7972345
722 Q>R No ClinGen
ExAC
gnomAD
CA395286883
rs1351938507
723 G>E No ClinGen
gnomAD
CA279645464
rs755776438
723 G>R No ClinGen
Ensembl
CA7972344
rs372401144
725 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395286785
rs1345142524
726 M>I No ClinGen
gnomAD
TCGA novel 727 S>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1273692380
CA395286738
729 P>S No ClinGen
gnomAD
CA7972341
rs760841873
730 R>G No ClinGen
ExAC
gnomAD
CA395286702
rs1298419223
731 D>N No ClinGen
gnomAD
CA395286640
rs1420682960
733 G>E No ClinGen
TOPMed
CA7972339
rs370464579
736 V>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA279645392
rs373105891
737 V>M No ClinGen
gnomAD
rs773079147
CA7972337
740 R>G No ClinGen
ExAC
TOPMed
gnomAD
CA7972335
rs769848907
740 R>K No ClinGen
ExAC
gnomAD
rs769848907
CA395286492
740 R>M No ClinGen
ExAC
gnomAD
rs780826829
CA7972333
741 P>A No ClinGen
ExAC
TOPMed
gnomAD
CA7972332
rs754700429
741 P>L No ClinGen
ExAC
gnomAD
rs746576599
CA279645339
742 F>L No ClinGen
ExAC
TOPMed
gnomAD
CA395286460
rs1279514063
742 F>S No ClinGen
TOPMed
CA279645337
rs965912826
744 G>E No ClinGen
TOPMed
gnomAD
TCGA novel 744 G>W Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
COSM557344
rs780482313
CA7972330
745 K>R lung [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
CA395286353
rs1358985353
746 R>S No ClinGen
TOPMed
CA279645326
rs974651725
747 P>A No ClinGen
TOPMed
rs1442285928
CA395286334
747 P>L No ClinGen
gnomAD
CA7972328
rs750797229
751 L>P No ClinGen
ExAC
CA7972329
rs376082233
751 L>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972327
rs757743340
753 Y>C No ClinGen
ExAC
gnomAD
CA7972326
rs757743340
753 Y>S No ClinGen
ExAC
gnomAD
CA395286163
rs1217609210
756 S>G No ClinGen
gnomAD
rs1338172381
CA395286094
758 G>A No ClinGen
gnomAD
rs1567350068
CA395286107
758 G>R No ClinGen
Ensembl
rs1233352099
CA395286043
760 S>G No ClinGen
TOPMed
CA279645274
rs979537533
762 R>C Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA7972324
rs142369579
762 R>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395285937
rs1358445642
764 M>I No ClinGen
gnomAD
rs752800344
CA7972322
766 R>G No ClinGen
ExAC
TOPMed
gnomAD
rs767763352
CA7972321
766 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs752800344
CA395285899
766 R>W No ClinGen
ExAC
TOPMed
gnomAD
CA279645203
rs960701650
768 T>I No ClinGen
TOPMed
CA395285852
rs1597638665
768 T>P No ClinGen
Ensembl
rs762720788
CA7972320
769 H>D No ClinGen
ExAC
gnomAD
rs773026685
CA7972319
770 H>D No ClinGen
ExAC
gnomAD
rs1476943700
CA395285816
770 H>R No ClinGen
gnomAD
rs1420483081
CA395285781
772 E>A No ClinGen
gnomAD
rs769900266
CA7972318
772 E>D No ClinGen
ExAC
gnomAD
CA395285788
rs1355606627
772 E>K No ClinGen
TOPMed
CA395285719
rs147734922
776 K>E No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972317
rs147734922
776 K>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395285689
rs1236307384
777 C>Y No ClinGen
gnomAD
CA7972316
rs145665207
778 G>D No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1382506714
CA395285623
781 G>V No ClinGen
TOPMed
rs768223317
CA7972315
782 K>R No ClinGen
ExAC
TOPMed
gnomAD
CA279645131
rs963226729
783 C>F No ClinGen
TOPMed
gnomAD
rs963226729
CA395285595
783 C>Y No ClinGen
TOPMed
gnomAD
CA7972314
rs746516370
785 G>V No ClinGen
ExAC
TOPMed
gnomAD
rs1214035374
CA395285551
786 R>G No ClinGen
TOPMed
COSM3794718
CA395285543
rs1314627262
786 R>K Variant assessed as Somatic; 0.0 impact. urinary_tract [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
CA7972312
rs771726233
787 S>G No ClinGen
ExAC
gnomAD
rs746270039
CA7972311
787 S>N No ClinGen
ExAC
TOPMed
gnomAD
CA395285486
rs1309181442
789 S>R No ClinGen
TOPMed
rs779203003
CA7972310
790 L>R No ClinGen
ExAC
gnomAD
rs1401168985
CA395285460
791 I>M No ClinGen
gnomAD
CA395285395
rs1464278201
795 R>I No ClinGen
TOPMed
gnomAD
rs777840147
CA7972307
795 R>S No ClinGen
ExAC
gnomAD
CA395285345
rs1165747341
798 T>K No ClinGen
gnomAD
CA7972305
rs199536276
800 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs767671587
CA395285225
807 D>H No ClinGen
ExAC
gnomAD
rs767671587
CA7972304
807 D>N No ClinGen
ExAC
gnomAD
CA395285208
rs1597638553
808 C>Y No ClinGen
Ensembl
CA7972303
rs759781177
809 G>E No ClinGen
ExAC
gnomAD
rs1456056436
CA395285194
810 K>N No ClinGen
gnomAD
rs772673796
CA279645038
810 K>Q No ClinGen
Ensembl
rs538818316
CA7972302
810 K>R No ClinGen
1000Genomes
ExAC
gnomAD
TCGA novel 811 S>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs765084098
CA7972301
811 S>T No ClinGen
ExAC
TOPMed
gnomAD
CA7972300
rs139344700
812 F>L No ClinGen
ESP
ExAC
CA7972299
rs776768102
813 N>S No ClinGen
ExAC
gnomAD
rs1287425161
CA395285171
814 D>N No ClinGen
gnomAD
CA395285160
rs763476151
815 S>C No ClinGen
TOPMed
gnomAD
CA279644995
rs763476151
815 S>F No ClinGen
TOPMed
gnomAD
rs1176767730
CA621663068
818 F>* No ClinGen
gnomAD
CA395285128
rs760144443
820 A>D No ClinGen
ExAC
gnomAD
rs768711275
CA7972298
820 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA7972297
rs760144443
820 A>V No ClinGen
ExAC
gnomAD
rs1369783027
CA395285126
821 H>N No ClinGen
gnomAD
rs997146346
CA279644991
822 Q>R No ClinGen
TOPMed
CA7972294
rs745496581
824 I>L No ClinGen
ExAC
TOPMed
gnomAD
rs1253292750
CA395285096
825 H>Y Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA7972293
rs569916415
826 T>A No ClinGen
1000Genomes
ExAC
gnomAD
CA7972292
rs749636452
826 T>I No ClinGen
ExAC
gnomAD
rs749636452
CA7972291
826 T>R No ClinGen
ExAC
gnomAD
CA279644958
rs762550611
828 E>G No ClinGen
Ensembl
CA7972290
rs778315570
829 K>T No ClinGen
ExAC
TOPMed
gnomAD
CA395285065
rs1380287051
830 P>T No ClinGen
gnomAD
CA279644937
rs946858117
831 Y>C Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
CA7972289
rs756610738
832 R>I No ClinGen
ExAC
TOPMed
gnomAD
rs150882404
CA7972287
834 G>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395285033
rs1268807889
835 E>* No ClinGen
gnomAD
CA7972286
rs755185597
835 E>D No ClinGen
ExAC
gnomAD
CA395285030
rs1430360062
835 E>V No ClinGen
TOPMed
CA7972285
rs751765632
836 C>Y No ClinGen
ExAC
TOPMed
gnomAD
CA395285021
rs1244782136
837 G>R No ClinGen
gnomAD
CA395285006
rs1205858760
839 C>R No ClinGen
TOPMed
gnomAD
CA395284946
rs1286293577
847 I>L No ClinGen
gnomAD
rs142423208
CA7972282
847 I>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1286293577
CA395284947
847 I>V No ClinGen
gnomAD
TCGA novel 848 I>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs752022614 848 I>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA395284931
rs1324244512
849 H>R No ClinGen
TOPMed
rs201757675
CA7972281
849 H>Y No ClinGen
ExAC
TOPMed
gnomAD
CA7972280
rs760615283
850 Q>R No ClinGen
ExAC
TOPMed
gnomAD
rs1401058673
CA395284917
851 R>T No ClinGen
gnomAD
rs774891458
CA7972279
COSM1233502
852 T>M Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7972276
rs774051331
853 H>R No ClinGen
ExAC
gnomAD
CA395284895
rs115298610
855 G>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7972274
rs115298610
855 G>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA395284873
rs1432083134
858 P>A No ClinGen
gnomAD
rs142344043
CA7972273
859 Y>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1195358639
CA395284850
861 C>Y No ClinGen
gnomAD
rs748650122
CA7972271
863 E>G No ClinGen
ExAC
gnomAD
CA395284829
rs1214402397
864 C>Y No ClinGen
TOPMed
gnomAD
TCGA novel 868 F>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs992212575
CA279644809
868 F>S No ClinGen
TOPMed
gnomAD
CA395284793
rs1256675118
869 T>A No ClinGen
gnomAD
CA7972269
rs61742936
871 S>G No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs990989745
CA279644795
874 F>L No ClinGen
Ensembl
CA7972268
rs377468868
875 S>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972266
rs146263630
876 A>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs753705688
CA7972265
876 A>V No ClinGen
ExAC
TOPMed
gnomAD
rs61742943
CA395284731
878 R>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs61742943
CA7972262
878 R>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972263
rs756005840
878 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
TCGA novel 880 V>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1346055214
CA395284708
882 T>A No ClinGen
TOPMed
CA7972260
rs759116702
883 G>V No ClinGen
ExAC
TOPMed
rs902799442
CA279644767
884 E>K No ClinGen
Ensembl
rs201613662
CA279644759
887 Y>C No ClinGen
1000Genomes
TOPMed
gnomAD
CA7972259
rs142448363
888 K>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs142448363
CA395284667
888 K>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs764164005
CA7972258
889 C>F No ClinGen
ExAC
gnomAD
rs1449559418
CA395284650
891 D>N No ClinGen
TOPMed
CA395284641
rs1191165413
892 C>R No ClinGen
TOPMed
gnomAD
rs373514402
CA7972257
892 C>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs373514402
CA7972256
892 C>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs369171450
CA7972255
893 E>V No ClinGen
ESP
ExAC
gnomAD
rs1199772164
CA395284628
894 K>E No ClinGen
TOPMed
gnomAD
rs1482343710
CA395284619
895 S>C No ClinGen
gnomAD
CA7972254
rs748616506
895 S>T No ClinGen
ExAC
gnomAD
rs1362373687
CA395284610
896 F>S No ClinGen
TOPMed
rs777261667
CA7972253
897 N>H No ClinGen
ExAC
TOPMed
gnomAD
rs769011354
CA7972252
897 N>S No ClinGen
ExAC
gnomAD
TCGA novel 898 N>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA279644734
rs997199076
899 C>G No ClinGen
TOPMed
rs138666050
CA7972251
899 C>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7972249
rs780230737
900 T>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA279644680
rs780230737
900 T>R No ClinGen
ExAC
TOPMed
gnomAD
CA279644669
rs932733214
903 R>* Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs746018009
CA7972247
903 R>Q No ClinGen
ExAC
TOPMed
gnomAD
CA7972246
rs150134367
905 H>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs755990861
CA7972245
906 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs781233246
CA7972243
907 R>S No ClinGen
ExAC
gnomAD
CA395284533
rs1368803048
908 I>M No ClinGen
gnomAD
CA395284538
rs1459284887
908 I>V No ClinGen
gnomAD
rs901233200
CA279644594
909 H>R No ClinGen
gnomAD
TCGA novel 912 E>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs754889766
CA7972242
914 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA395284495
rs1463655391
914 P>S No ClinGen
gnomAD
CA395284487
rs551460206
915 Y>* No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs751093524
CA7972241
915 Y>C No ClinGen
ExAC
gnomAD
rs867258537
CA279644562
916 G>E No ClinGen
Ensembl
TCGA novel 917 C>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA395284471
rs1256447589
918 A>P No ClinGen
gnomAD
rs762599191
CA7972239
919 Q>* No ClinGen
ExAC
gnomAD
rs1265187933
CA395284448
921 G>D No ClinGen
gnomAD
CA395284451
rs1357525199
921 G>S No ClinGen
gnomAD
rs750034251
CA7972238
922 K>R No ClinGen
ExAC
TOPMed
gnomAD
CA7972237
COSM969146
rs764792410
923 R>C Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs878895014
CA279644518
923 R>H No ClinGen
TOPMed
gnomAD
rs878895014
CA395284435
923 R>L No ClinGen
TOPMed
gnomAD
CA279644510
rs1047624859
925 S>R No ClinGen
Ensembl
CA395284417
rs1442939783
926 K>* No ClinGen
TOPMed
CA395284413
rs1446968989
926 K>N No ClinGen
gnomAD
CA395284395
rs1163194817
927 S>N No ClinGen
TOPMed
rs945201512
CA279644493
929 V>D No ClinGen
TOPMed
CA7972235
rs776836279
930 L>H No ClinGen
ExAC
gnomAD
CA7972233
rs369090600
931 T>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA395284336
rs369090600
931 T>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs369090600
CA7972234
931 T>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1395663283
CA395284331
932 K>Q No ClinGen
TOPMed
rs376654450
CA7972231
933 H>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs141758597
CA7972229
934 R>Q No ClinGen
ESP
ExAC
gnomAD
CA7972230
rs772217177
934 R>W No ClinGen
ExAC
TOPMed
gnomAD
CA395284287
rs1315059833
935 E>G No ClinGen
gnomAD
rs771030814
CA279644413
937 H>L No ClinGen
ExAC
TOPMed
gnomAD
CA395284227
rs1567349618
937 H>Q No ClinGen
Ensembl
rs771030814
CA7972227
937 H>R No ClinGen
ExAC
TOPMed
gnomAD
rs148807631
CA7972225
942 P>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs751432855
CA7972223
944 P>L No ClinGen
ExAC
gnomAD
CA7972224
rs754941718
944 P>S No ClinGen
ExAC
gnomAD
TCGA novel 945 H>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1361201671
CA395284010
946 P>A No ClinGen
TOPMed
rs1356286944
CA395284003
946 P>L No ClinGen
gnomAD
rs7197424
CA7972220
VAR_057460
947 P>S No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs761321272
CA7972218
949 L>V No ClinGen
ExAC
gnomAD
rs202019779
CA7972215
951 C>R No ClinGen
1000Genomes
ExAC
gnomAD
CA395283901
rs1322470765
952 P>L No ClinGen
gnomAD
CA279644297
rs982966510
952 P>S No ClinGen
TOPMed
CA279644270
rs772698016
953 E>D No ClinGen
ExAC
TOPMed
gnomAD
rs1021243869
CA279644264
956 H>Y No ClinGen
Ensembl
CA7972212
rs199651270
957 K>E No ClinGen
ExAC
TOPMed
gnomAD
CA395283762
rs1555489218
961 D>N No ClinGen
Ensembl
rs774275525
CA7972211
962 E>Q No ClinGen
ExAC
gnomAD
rs1460281264
CA395283722
963 F>C No ClinGen
TOPMed
CA7972210
rs771209111
964 R>K No ClinGen
ExAC
gnomAD
CA7972209
rs749433110
965 K>R No ClinGen
ExAC
TOPMed
gnomAD
CA279644241
rs958276998
966 T>N No ClinGen
Ensembl
rs1386411487
CA395283668
967 F>S No ClinGen
TOPMed
gnomAD
rs768382257
CA7972207
968 F>C No ClinGen
ExAC
TOPMed
gnomAD
CA395283657
rs768382257
968 F>W No ClinGen
ExAC
TOPMed
gnomAD

No associated diseases with Q63HK3

1 regional properties for Q63HK3

Type Name Position InterPro Accession
domain Fork head domain 174 - 266 IPR001766

Functions

Description
EC Number
Subcellular Localization
  • Nucleus
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

1 GO annotations of cellular component

Name Definition
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.

3 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.
metal ion binding Binding to a metal ion.
RNA polymerase II cis-regulatory region sequence-specific DNA binding Binding to a specific upstream regulatory DNA sequence (transcription factor recognition sequence or binding site) located in cis relative to the transcription start site (i.e., on the same strand of DNA) of a gene transcribed by RNA polymerase II.

1 GO annotations of biological process

Name Definition
regulation of transcription by RNA polymerase II Any process that modulates the frequency, rate or extent of transcription mediated by RNA polymerase II.

177 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
P08151 GLI1 Zinc finger protein GLI1 Homo sapiens (Human) PR
Q9UFB7 ZBTB47 Zinc finger and BTB domain-containing protein 47 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
Q96SZ4 ZSCAN10 Zinc finger and SCAN domain-containing protein 10 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
Q8TBJ5 FEZF2 Fez family zinc finger protein 2 Homo sapiens (Human) PR
Q96SR6 ZNF382 Zinc finger protein 382 Homo sapiens (Human) PR
Q9ULJ3 ZBTB21 Zinc finger and BTB domain-containing protein 21 Homo sapiens (Human) PR
O75840 KLF7 Krueppel-like factor 7 Homo sapiens (Human) PR
Q13127 REST RE1-silencing transcription factor Homo sapiens (Human) PR
Q8IZM8 ZNF654 Zinc finger protein 654 Homo sapiens (Human) PR
Q14526 HIC1 Hypermethylated in cancer 1 protein Homo sapiens (Human) PR
Q06889 EGR3 Early growth response protein 3 Homo sapiens (Human) PR
Q08ER8 ZNF543 Zinc finger protein 543 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
Q96BV0 ZNF775 Zinc finger protein 775 Homo sapiens (Human) PR
Q5FWF6 ZNF789 Zinc finger protein 789 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
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
Q9Y2D9 ZNF652 Zinc finger protein 652 Homo sapiens (Human) PR
Q5TC79 ZBTB37 Zinc finger and BTB domain-containing protein 37 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
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
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
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
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
A1YPR0 ZBTB7C Zinc finger and BTB domain-containing protein 7C 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
Q8NAM6 ZSCAN4 Zinc finger and SCAN domain-containing protein 4 Homo sapiens (Human) PR
Q9NPC7 MYNN Myoneurin Homo sapiens (Human) PR
O14978 ZNF263 Zinc finger protein 263 Homo sapiens (Human) PR
P17022 ZNF18 Zinc finger protein 18 Homo sapiens (Human) PR
Q6P9G9 ZNF449 Zinc finger protein 449 Homo sapiens (Human) PR
O60304 ZNF500 Zinc finger protein 500 Homo sapiens (Human) PR
Q9NX65 ZSCAN32 Zinc finger and SCAN domain-containing protein 32 Homo sapiens (Human) PR
Q96IT1 ZNF496 Zinc finger protein 496 Homo sapiens (Human) PR
O14771 ZNF213 Zinc finger protein 213 Homo sapiens (Human) PR
O95125 ZNF202 Zinc finger protein 202 Homo sapiens (Human) PR
Q8IWY8 ZSCAN29 Zinc finger and SCAN domain-containing protein 29 Homo sapiens (Human) PR
Q8N0Y2 ZNF444 Zinc finger protein 444 Homo sapiens (Human) PR
A6NGD5 ZSCAN5C Zinc finger and SCAN domain-containing protein 5C Homo sapiens (Human) PR
A6NJL1 ZSCAN5B Zinc finger and SCAN domain-containing protein 5B Homo sapiens (Human) PR
Q8NF99 ZNF397 Zinc finger protein 397 Homo sapiens (Human) PR
Q86XF7 ZNF575 Zinc finger protein 575 Homo sapiens (Human) PR
Q9NWS9 ZNF446 Zinc finger protein 446 Homo sapiens (Human) PR
Q96N95 ZNF396 Zinc finger protein 396 Homo sapiens (Human) PR
Q9UL58 ZNF215 Zinc finger protein 215 Homo sapiens (Human) PR
P17029 ZKSCAN1 Zinc finger protein with KRAB and SCAN domains 1 Homo sapiens (Human) PR
Q53GI3 ZNF394 Zinc finger protein 394 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
Q6NSZ9 ZSCAN25 Zinc finger and SCAN domain-containing protein 25 Homo sapiens (Human) PR
Q9UNY5 ZNF232 Zinc finger protein 232 Homo sapiens (Human) PR
P17028 ZNF24 Zinc finger protein 24 Homo sapiens (Human) PR
P49910 ZNF165 Zinc finger protein 165 Homo sapiens (Human) PR
Q15776 ZKSCAN8 Zinc finger protein with KRAB and SCAN domains 8 Homo sapiens (Human) PR
Q9H9D4 ZNF408 Zinc finger protein 408 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
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
MAVALDSQID APLEVEGCLI MKVEKDPEWA SEPILEGSDS SETFRKCFRQ FCYEDVTGPH
70 80 90 100 110 120
EAFSKLWELC CRWLKPEMRS KEQILELLVI EQFLTILPEK IQAWAQKQCP QSGEEAVALV
130 140 150 160 170 180
VHLEKETGRL RQQVSSPVHR EKHSPLGAAW EVADFQPEQV ETQPRAVSRE EPGSLHSGHQ
190 200 210 220 230 240
EQLNRKRERR PLPKNARPSP WVPALADEWN TLDQEVTTTR LPAGSQEPVK DVHVARGFSY
250 260 270 280 290 300
RKSVHQIPAQ RDLYRDFRKE NVGNVVSLGS AVSTSNKITR LEQRKEPWTL GLHSSNKRSI
310 320 330 340 350 360
LRSNYVKEKS VHAIQVPARS AGKTWREQQQ WGLEDEKIAG VHWSYEETKT FLAILKESRF
370 380 390 400 410 420
YETLQACPRN SQVYGAVAEW LRECGFLRTP EQCRTKFKSL QKSYRKVRNG HMLEPCAFFE
430 440 450 460 470 480
DMDALLNPAA RAPSTDKPKE MIPVPRLKRI AISAKEHISL VEEEEAAEDS DDDEIGIEFI
490 500 510 520 530 540
RKSEIHGAPV LFQNLSGVHW GYEETKTFLD ILRETRFYEA LQACHRKSKL YGAVAEQLRE
550 560 570 580 590 600
CGFLRTPEQC RTKFKSLQKS YRKVKNGHVL ESCAFYKEMD ALINSRASAP SPSTPEEVPS
610 620 630 640 650 660
PSRQERGGIE VEPQEPTGWE PEETSQEAVI EDSCSERMSE EEIVQEPEFQ GPPGLLQSPN
670 680 690 700 710 720
DFEIGSSIKE DPTQIVYKDM EQHRALIEKS KRVVSQSTDP SKYRKRECIS GRQWENLQGI
730 740 750 760 770 780
RQGKPMSQPR DLGKAVVHQR PFVGKRPYRL LKYGESFGRS TRLMCRMTHH KENPYKCGVC
790 800 810 820 830 840
GKCFGRSRSL IRHQRIHTGE KPFKCLDCGK SFNDSSNFGA HQRIHTGEKP YRCGECGKCF
850 860 870 880 890 900
SQSSSLIIHQ RTHTGEKPYQ CGECGKSFTN SSHFSAHRRV HTGENPYKCV DCEKSFNNCT
910 920 930 940 950 960
RFREHRRIHT GEKPYGCAQC GKRFSKSSVL TKHREVHVRE KPLPHPPSLY CPENPHKGKT
DEFRKTF