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 Q8IWY8

Entry ID Method Resolution Chain Position Source
AF-Q8IWY8-F1 Predicted AlphaFoldDB

724 variants for Q8IWY8

Variant ID(s) Position Change Description Diseaes Association Provenance
rs1377520189
CA392110589
2 M>I No ClinGen
gnomAD
CA392110565
rs1021267379
3 A>D No ClinGen
TOPMed
gnomAD
TCGA novel 3 A>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA392110576
rs1166879692
3 A>T No ClinGen
gnomAD
rs1021267379
CA269978538
3 A>V No ClinGen
TOPMed
gnomAD
CA269978529
rs773356187
4 K>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA392110549
rs773356187
4 K>T No ClinGen
TOPMed
gnomAD
rs1422552155
CA392110500
6 A>G No ClinGen
gnomAD
rs192858183
CA7523597
6 A>P No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1236081814
CA392110463
9 E>Q No ClinGen
TOPMed
CA392110436
rs1284257277
10 N>D No ClinGen
TOPMed
rs1317728909
CA392110397
11 G>D No ClinGen
TOPMed
CA7523595
rs140261564
12 T>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1194860322
CA392110351
14 S>Y No ClinGen
gnomAD
rs768203572
CA7523593
15 E>Q No ClinGen
ExAC
CA7523591
rs746612822
16 T>N No ClinGen
ExAC
TOPMed
gnomAD
rs746612822
CA392110321
16 T>S No ClinGen
ExAC
TOPMed
gnomAD
CA269978461
rs577380357
17 F>L No ClinGen
gnomAD
CA269978470
rs541663171
17 F>Y No ClinGen
Ensembl
CA7523590
rs779852952
18 R>* Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA269978444
rs958076670
19 Q>H No ClinGen
TOPMed
gnomAD
CA392110246
rs1415484435
22 R>G No ClinGen
gnomAD
rs371123760
CA7523587
23 R>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA392110193
rs1238052006
25 H>Y No ClinGen
gnomAD
CA7523586
rs778773510
31 G>W No ClinGen
ExAC
gnomAD
COSM1168806
CA7523584
rs752724376
33 R>Q pancreas [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
rs767577009
CA7523583
36 F>C No ClinGen
ExAC
gnomAD
rs755273991
CA7523582
37 S>I No ClinGen
ExAC
TOPMed
gnomAD
CA7523581
rs145523535
38 Q>* No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1457141763
CA392109973
38 Q>R No ClinGen
TOPMed
rs1438076068
CA392109810
45 R>G No ClinGen
TOPMed
gnomAD
rs763463071
CA7523579
45 R>Q No ClinGen
ExAC
gnomAD
CA392109807
rs1438076068
45 R>W No ClinGen
TOPMed
gnomAD
rs199823856
CA7523576
50 E>A No ClinGen
ExAC
TOPMed
gnomAD
rs199823856
CA7523575
50 E>G No ClinGen
ExAC
TOPMed
gnomAD
rs1273811782
CA392109682
50 E>K No ClinGen
gnomAD
rs199823856
CA392109667
50 E>V No ClinGen
ExAC
TOPMed
gnomAD
rs1595470119
CA392109635
51 V>G No ClinGen
Ensembl
CA392109625
rs1280566361
52 R>C No ClinGen
TOPMed
rs201276901
CA7523573
52 R>H No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA392109630
rs1280566361
52 R>S No ClinGen
TOPMed
rs775168852
CA7523572
53 T>A No ClinGen
ExAC
gnomAD
rs1331069563
CA392109507
57 I>M No ClinGen
gnomAD
rs1340956253
CA392109512
57 I>T No ClinGen
TOPMed
gnomAD
rs1385519738
CA392109485
59 E>G No ClinGen
gnomAD
TCGA novel 59 E>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs745728301
CA7523570
63 L>P No ClinGen
ExAC
rs1463445854
CA392109402
65 Q>H No ClinGen
gnomAD
CA269978381
rs375291931
66 F>L No ClinGen
ESP
rs749200711
CA392109359
69 V>I No ClinGen
ExAC
gnomAD
rs749200711
CA7523567
69 V>L No ClinGen
ExAC
gnomAD
CA7523566
rs781161811
71 P>L No ClinGen
ExAC
gnomAD
rs1487303858
CA392109287
73 E>D No ClinGen
TOPMed
rs1196305818
CA392109265
74 I>M No ClinGen
gnomAD
rs1195551413
CA392109273
74 I>N No ClinGen
TOPMed
rs373539308
CA7523564
77 W>* No ClinGen
ESP
ExAC
rs766768290
CA7523563
78 V>I No ClinGen
ExAC
gnomAD
CA392109177
rs758692064
79 Q>* No ClinGen
ExAC
TOPMed
gnomAD
CA269978287
rs758692064
79 Q>E No ClinGen
ExAC
TOPMed
gnomAD
CA7523562
rs758692064
79 Q>K No ClinGen
ExAC
TOPMed
gnomAD
rs1327038972
CA392109173
79 Q>R No ClinGen
gnomAD
rs866467782
CA269978275
82 C>F No ClinGen
Ensembl
CA392109095
rs369750307
82 C>G No ClinGen
ExAC
TOPMed
gnomAD
CA7523560
rs369750307
82 C>R No ClinGen
ExAC
TOPMed
gnomAD
rs762255048
CA7523559
83 P>T No ClinGen
ExAC
gnomAD
rs369660593
CA7523558
84 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1157573899
CA392109004
85 N>S No ClinGen
TOPMed
CA392108930
rs1418471920
88 E>K No ClinGen
TOPMed
rs760234602
CA7523556
92 L>F No ClinGen
ExAC
gnomAD
CA7523555
rs760234602
92 L>V No ClinGen
ExAC
gnomAD
CA392108790
rs1387103172
93 V>A No ClinGen
gnomAD
CA7523551
rs774037467
95 D>Y No ClinGen
ExAC
TOPMed
gnomAD
CA7523549
rs749006936
96 L>I No ClinGen
ExAC
TOPMed
gnomAD
CA7523550
rs749006936
96 L>V No ClinGen
ExAC
TOPMed
gnomAD
CA392108681
rs1170501287
98 R>G No ClinGen
gnomAD
rs1359529853
CA392108658
98 R>S No ClinGen
gnomAD
CA392108669
rs1247445559
98 R>T No ClinGen
TOPMed
gnomAD
rs376561845
CA7523546
99 E>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7523548
rs200584649
99 E>K No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs200584649
CA7523547
99 E>Q No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA392108624
rs1218707590
100 P>A No ClinGen
TOPMed
TCGA novel 100 P>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA392108572
rs1195291653
102 R>T No ClinGen
gnomAD
rs3809482
CA392108536
104 R>* No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
VAR_059949
CA7523545
rs3809482
104 R>G No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA392108521
rs1241450797
104 R>S No ClinGen
gnomAD
rs1216393621
CA392108510
105 S>T No ClinGen
gnomAD
rs1447703974
CA392108507
105 S>Y No ClinGen
gnomAD
COSM1373013
rs1595469922
CA392108468
106 S>L large_intestine [Cosmic] No ClinGen
cosmic curated
Ensembl
CA392108481
rs1286390445
106 S>P No ClinGen
gnomAD
rs748044714
CA7523527
107 V>I No ClinGen
ExAC
gnomAD
CA392107974
rs1346773607
109 V>I No ClinGen
TOPMed
CA7523526
rs576124859
112 K>E No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs772315092
CA7523525
114 Q>* No ClinGen
ExAC
gnomAD
rs779251291
CA7523523
117 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA392107785
rs1411537752
117 R>H No ClinGen
gnomAD
CA7523521
rs754233342
118 L>F No ClinGen
ExAC
gnomAD
rs757414806
CA392107765
118 L>V No ClinGen
ExAC
TOPMed
gnomAD
rs778053562
CA7523520
120 K>M No ClinGen
ExAC
gnomAD
CA392107694
rs1205679022
CA392107692
121 M>I No ClinGen
gnomAD
CA7523518
rs753162944
121 M>T No ClinGen
ExAC
gnomAD
rs767981508
CA7523516
122 T>S No ClinGen
ExAC
gnomAD
CA7523515
rs759135715
123 P>S No ClinGen
ExAC
gnomAD
rs376557252
CA7523514
124 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1566884880 124 P>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 127 S>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1217020230
CA392107540
129 E>A No ClinGen
TOPMed
rs1288479087
CA392107551
129 E>K No ClinGen
TOPMed
gnomAD
rs1288479087
CA392107548
129 E>Q No ClinGen
TOPMed
gnomAD
CA7523512
rs762449386
130 L>S No ClinGen
ExAC
gnomAD
rs151307138
CA7523509
132 S>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
CA392107448
rs776755616
133 V>F No ClinGen
ExAC
TOPMed
gnomAD
CA7523507
rs776755616
133 V>I No ClinGen
ExAC
TOPMed
gnomAD
rs199628783
CA7523505
134 R>Q No ClinGen
1000Genomes
ExAC
gnomAD
COSM1373012
CA7523506
rs768461400
134 R>W Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
rs1401041732
CA392107341
137 S>P No ClinGen
TOPMed
rs1250089128
CA392107300
138 V>A No ClinGen
TOPMed
gnomAD
CA7523503
CA392107311
rs749449553
138 V>L No ClinGen
ExAC
TOPMed
gnomAD
CA7523502
rs749449553
138 V>M No ClinGen
ExAC
TOPMed
gnomAD
CA392107257
rs1353395313
140 P>R No ClinGen
gnomAD
CA7523501
rs200482375
142 P>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs28493274
COSM1373011
CA392107168
143 R>S Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
gnomAD
CA7523500
rs756501449
143 R>T No ClinGen
ExAC
gnomAD
CA392107150
rs1213414630
144 G>V No ClinGen
gnomAD
rs1566884803
CA392107132
145 V>A No ClinGen
Ensembl
rs936695329
CA269977630
145 V>I No ClinGen
gnomAD
rs144922562
CA7523499
146 P>S No ClinGen
ESP
ExAC
TOPMed
CA7523497
rs755371545
147 K>N No ClinGen
ExAC
gnomAD
CA392107013
rs1195616284
148 K>R No ClinGen
Ensembl
rs558053205
CA7523495
149 E>D No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA269977602
rs925201934
149 E>K No ClinGen
TOPMed
gnomAD
CA7523494
rs758115046
150 R>M No ClinGen
ExAC
rs764938746
CA7523492
159 Q>* No ClinGen
ExAC
gnomAD
rs776504510
CA7523490
162 M>T No ClinGen
ExAC
gnomAD
CA7523491
rs761717947
162 M>V No ClinGen
ExAC
gnomAD
CA392106402
rs1451805425
164 P>L No ClinGen
gnomAD
CA7523489
rs770899128
166 E>D No ClinGen
ExAC
gnomAD
CA7523488
rs760518253
167 K>Q No ClinGen
ExAC
TOPMed
rs1160172191
CA392106095
173 R>T No ClinGen
gnomAD
rs753746345
CA7523470
175 G>A No ClinGen
ExAC
gnomAD
CA7523485
rs770885404
175 G>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs763775948
CA7523468
178 F>I No ClinGen
ExAC
gnomAD
rs968176116
CA269976121
182 G>C No ClinGen
TOPMed
CA392104527
rs968176116
182 G>S No ClinGen
TOPMed
rs1372771215
CA392104500
183 V>G No ClinGen
TOPMed
CA7523466
rs775321384
185 S>F No ClinGen
ExAC
gnomAD
CA7523464
rs141062118
186 R>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1349849738
CA392104405
188 E>K No ClinGen
gnomAD
CA392104374
rs773208736
189 Q>E Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7523461
rs770067127
189 Q>H No ClinGen
ExAC
TOPMed
gnomAD
CA7523462
rs773208736
189 Q>K No ClinGen
ExAC
TOPMed
gnomAD
CA7523460
rs762006823
191 E>K No ClinGen
ExAC
gnomAD
CA392104331
rs1566883952
191 E>V No ClinGen
Ensembl
rs1435534780
CA392104317
193 W>R No ClinGen
TOPMed
gnomAD
TCGA novel 194 I>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA269976083
rs1020072427
196 D>N No ClinGen
TOPMed
VAR_057459
CA7523455
rs3917221
199 G>S No ClinGen
UniProt
1000Genomes
ESP
TOPMed
dbSNP
rs145368334
CA7523454
200 S>F No ClinGen
ESP
ExAC
rs540688919
CA7523452
202 E>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs780443175
CA7523453
202 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs531848637
CA7523451
203 K>E No ClinGen
ExAC
gnomAD
rs139941693
CA7523450
204 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs1005261450
CA269976033
206 P>L No ClinGen
Ensembl
CA7523449
rs757020953
207 S>I No ClinGen
ExAC
TOPMed
gnomAD
CA7523447
rs777442540
211 I>L No ClinGen
ExAC
gnomAD
CA7523446
rs755884310
211 I>T No ClinGen
ExAC
TOPMed
gnomAD
rs777442540
CA269976012
211 I>V No ClinGen
ExAC
gnomAD
rs1027944571
CA269975991
214 R>T No ClinGen
Ensembl
rs752477835
CA7523444
215 R>* No ClinGen
ExAC
gnomAD
CA7523443
rs767359082
215 R>Q No ClinGen
ExAC
gnomAD
rs1342502555
CA392104040
216 V>G No ClinGen
gnomAD
rs1327026015
CA392104016
218 A>S No ClinGen
gnomAD
TCGA novel 219 D>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA392103977
rs1397641673
221 L>S No ClinGen
gnomAD
rs750557726
CA7523441
222 P>T No ClinGen
ExAC
gnomAD
rs1165025712
CA392103937
224 K>R No ClinGen
gnomAD
rs776745172
CA392103896
226 D>E No ClinGen
ExAC
TOPMed
gnomAD
CA7523439
rs762058112
226 D>N No ClinGen
ExAC
gnomAD
CA7523437
rs144725049
228 R>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA269975908
rs879099839
228 R>T No ClinGen
Ensembl
rs1038826924
CA269975900
229 S>N No ClinGen
TOPMed
gnomAD
rs772767271
CA7523433
232 E>D No ClinGen
ExAC
gnomAD
CA7523434
rs73401911
232 E>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA392103795
rs1566883850
235 H>Q No ClinGen
Ensembl
rs759020326
CA269975873
235 H>Y No ClinGen
TOPMed
gnomAD
rs746356675
CA7523432
236 W>* No ClinGen
ExAC
gnomAD
CA7523431
rs778609011
238 F>L No ClinGen
ExAC
gnomAD
rs770598072
CA7523430
241 E>K No ClinGen
ExAC
TOPMed
gnomAD
CA392103746
rs1333828912
242 K>E No ClinGen
gnomAD
rs561229494
CA392103743
242 K>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs561229494
CA7523429
242 K>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1327160119
CA392103726
245 G>C No ClinGen
gnomAD
CA7523426
rs746567067
246 V>A No ClinGen
ExAC
TOPMed
gnomAD
rs1433413358
CA392103676
248 W>L No ClinGen
TOPMed
gnomAD
CA7523424
rs781026218
249 G>D No ClinGen
ExAC
gnomAD
CA7523425
rs376441921
249 G>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA392103649
rs1189083721
250 Y>D No ClinGen
gnomAD
CA392103629
rs1453504496
251 E>G No ClinGen
gnomAD
rs754955840
CA7523423
254 R>G No ClinGen
ExAC
TOPMed
gnomAD
rs139569236
CA7523422
255 T>M No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs139569236
CA392103558
255 T>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs150573966
CA7523421
256 L>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs753893132
CA7523419
258 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7523418
rs142621348
259 I>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7523417
rs373614639
260 L>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA269975809
rs769125986
261 S>T No ClinGen
Ensembl
TCGA novel 265 F>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1276011286
CA392103262
268 A>T No ClinGen
TOPMed
gnomAD
rs767963686
CA7523414
268 A>V No ClinGen
ExAC
gnomAD
CA392103233
rs1343903657
269 L>F No ClinGen
gnomAD
rs759941128
CA7523413
269 L>P No ClinGen
ExAC
TOPMed
gnomAD
rs1342023929
CA392103208
270 R>K No ClinGen
TOPMed
rs775020957
CA7523411
271 N>H No ClinGen
ExAC
gnomAD
CA392103149
rs1171362939
271 N>K No ClinGen
gnomAD
rs1595468072
CA392103175
271 N>T No ClinGen
Ensembl
rs1262185817
CA392103131
272 C>F No ClinGen
Ensembl
rs1433934378
CA392103091
273 H>Q No ClinGen
gnomAD
TCGA novel 273 H>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs748751481
CA7523409
274 R>S No ClinGen
ExAC
gnomAD
CA7523408
rs772772295
275 N>Y No ClinGen
ExAC
CA392102987
rs1241400400
277 Q>* No ClinGen
TOPMed
gnomAD
CA392102991
rs1241400400
277 Q>E No ClinGen
TOPMed
gnomAD
CA392102994
rs1241400400
277 Q>K No ClinGen
TOPMed
gnomAD
rs747811705
CA7523406
278 V>M No ClinGen
ExAC
gnomAD
rs1465712659
CA392102901
279 Y>N No ClinGen
TOPMed
rs781002210
CA7523405
281 A>T No ClinGen
ExAC
gnomAD
CA7523404
rs754795408
282 V>A No ClinGen
ExAC
gnomAD
rs758356056
CA7523401
285 R>Q No ClinGen
ExAC
gnomAD
CA7523402
rs779975572
285 R>W No ClinGen
ExAC
TOPMed
gnomAD
COSM1678408
CA392102741
rs1270061721
CA392102739
287 R>S large_intestine [Cosmic] No ClinGen
cosmic curated
TOPMed
gnomAD
CA392102718
rs1400152829
288 E>* No ClinGen
gnomAD
CA7523395
rs769580660
293 R>P No ClinGen
ExAC
gnomAD
CA7523394
rs769580660
293 R>Q No ClinGen
ExAC
gnomAD
CA7523397
rs767799510
COSM961952
293 R>W Variant assessed as Somatic; 0.0 impact. central_nervous_system endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs767059638
CA7523393
294 T>I No ClinGen
ExAC
TOPMed
gnomAD
rs772644551
CA7523391
295 L>P No ClinGen
ExAC
rs1595468012
CA392102509
296 E>K No ClinGen
Ensembl
CA392102483
rs1168411746
297 Q>* No ClinGen
TOPMed
gnomAD
rs1168411746
CA392102486
297 Q>E No ClinGen
TOPMed
gnomAD
CA7523389
rs138128428
297 Q>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs776283994
CA7523387
298 C>R No ClinGen
ExAC
gnomAD
rs768236774
CA7523386
299 R>Q No ClinGen
ExAC
gnomAD
rs1185839817
CA392102448
299 R>W No ClinGen
TOPMed
gnomAD
rs746876609
CA7523385
300 T>A No ClinGen
ExAC
TOPMed
gnomAD
rs1212686192
CA392102429
300 T>I No ClinGen
gnomAD
rs746876609
CA392102437
300 T>P No ClinGen
ExAC
TOPMed
gnomAD
rs1306124515
CA392102413
301 K>N No ClinGen
gnomAD
rs779816000
CA7523384
302 F>V No ClinGen
ExAC
CA392102391
rs1307199286
303 K>* No ClinGen
TOPMed
rs928012902
CA269975631
303 K>R No ClinGen
gnomAD
rs1319436808
CA392102364
304 G>A No ClinGen
gnomAD
rs1219763596
CA392102368
304 G>S No ClinGen
gnomAD
CA7523383
rs758318956
308 S>G No ClinGen
ExAC
gnomAD
CA392102292
rs1348189569
308 S>R No ClinGen
TOPMed
rs745788661
CA392102272
309 Y>* No ClinGen
ExAC
gnomAD
CA392102280
rs1304218926
309 Y>C No ClinGen
gnomAD
CA392102287
rs1366060784
309 Y>H No ClinGen
gnomAD
rs778677754
CA392102267
310 R>G No ClinGen
ExAC
TOPMed
gnomAD
rs199803410
CA7523379
310 R>Q No ClinGen
TOPMed
gnomAD
CA7523381
rs778677754
310 R>W No ClinGen
ExAC
TOPMed
gnomAD
CA269975604
rs1027610683
312 V>A No ClinGen
Ensembl
rs1415512343
CA392102218
313 K>R No ClinGen
gnomAD
CA392102181
COSM1478135
rs1414884019
315 G>D Variant assessed as Somatic; 0.0 impact. breast [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs143066980
CA7523376
315 G>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1566883590
CA392102122
319 E>Q No ClinGen
Ensembl
rs766743066
CA7523373
322 P>L No ClinGen
ExAC
gnomAD
rs752026910
CA7523374
322 P>S No ClinGen
ExAC
gnomAD
CA269975586
rs1008661276
325 E>K No ClinGen
Ensembl
rs1459497761
CA392101987
326 E>D No ClinGen
gnomAD
CA7523372
rs553606667
327 M>I No ClinGen
1000Genomes
ExAC
gnomAD
CA392101917
rs1232156640
331 M>L No ClinGen
gnomAD
CA7523371
rs750968798
333 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA392101864
rs1314489660
334 Q>* No ClinGen
gnomAD
CA392101852
rs1221685637
334 Q>L No ClinGen
gnomAD
CA392101841
rs1372107490
335 V>L No ClinGen
gnomAD
CA7523370
rs765609657
336 I>L No ClinGen
ExAC
gnomAD
rs1413054963
CA392101801
337 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA392101764
rs1392205433
340 S>G No ClinGen
gnomAD
rs1325130587
CA392101753
340 S>R No ClinGen
gnomAD
rs776117761
CA7523368
342 G>D No ClinGen
ExAC
gnomAD
CA392101704
rs1432671202
343 L>V No ClinGen
TOPMed
CA7523366
rs760301969
344 E>K No ClinGen
ExAC
gnomAD
CA392101661
rs1417590950
345 A>S No ClinGen
gnomAD
CA7523365
rs370250426
345 A>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1179669692
CA392101609
347 A>V No ClinGen
gnomAD
rs1379241429
CA392101591
348 S>F No ClinGen
TOPMed
CA7523364
rs771934402
349 H>L No ClinGen
ExAC
gnomAD
rs1466510958
CA392101523
351 G>S No ClinGen
TOPMed
TCGA novel 352 L>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7523362
rs557927379
353 V>A No ClinGen
ExAC
TOPMed
gnomAD
CA392101441
rs1488544029
354 G>D No ClinGen
TOPMed
gnomAD
rs770707647
CA7523361
355 S>T No ClinGen
ExAC
gnomAD
CA7523358
rs755298355
356 D>G No ClinGen
ExAC
gnomAD
rs781407532
COSM3401743
CA7523359
356 D>N Variant assessed as Somatic; 0.0 impact. central_nervous_system [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
rs780096611
CA7523356
357 A>G No ClinGen
ExAC
TOPMed
gnomAD
CA7523357
rs377129589
357 A>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 359 T>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA392101250
rs1387251295
361 E>K No ClinGen
TOPMed
gnomAD
rs750691361
CA7523354
363 G>A No ClinGen
ExAC
gnomAD
CA269975516
rs772248793
363 G>W No ClinGen
Ensembl
rs765774960
CA7523353
364 Q>H No ClinGen
ExAC
gnomAD
rs753398749
CA7523352
365 R>S No ClinGen
ExAC
gnomAD
rs1421955508
CA392101097
368 Q>* No ClinGen
TOPMed
gnomAD
rs568348919
CA7523348
369 H>P No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7523349
rs568348919
369 H>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7523350
rs763566787
369 H>Y No ClinGen
ExAC
CA7523347
rs771566330
370 E>K No ClinGen
ExAC
gnomAD
rs896662041
CA269975464
372 G>V No ClinGen
TOPMed
CA392100871
rs1488287720
375 E>K No ClinGen
TOPMed
CA7523345
rs759381129
377 V>M No ClinGen
ExAC
gnomAD
CA7523344
rs372802206
379 Q>* No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs770959404
CA7523343
379 Q>H No ClinGen
ExAC
gnomAD
CA392100745
rs1216249586
379 Q>R No ClinGen
Ensembl
CA392100695
rs1595467828
381 S>A No ClinGen
Ensembl
rs1218316867
CA392100684
381 S>F No ClinGen
gnomAD
rs1269600048
CA392100659
382 D>E No ClinGen
TOPMed
CA7523342
rs749214283
384 D>V No ClinGen
ExAC
gnomAD
rs1313895896
CA392100545
386 M>V No ClinGen
gnomAD
TCGA novel 390 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7523340
rs548365788
390 A>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7523337
rs758479000
391 T>I No ClinGen
ExAC
TOPMed
gnomAD
rs758479000
CA7523338
391 T>N No ClinGen
ExAC
TOPMed
gnomAD
CA269975421
rs948395910
392 P>L No ClinGen
Ensembl
rs750860549
CA7523336
393 Q>* No ClinGen
ExAC
TOPMed
gnomAD
CA392100352
rs750860549
393 Q>K No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 393 Q>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1373810179
CA392100297
395 P>L No ClinGen
gnomAD
CA7523334
rs779129277
397 S>L No ClinGen
ExAC
TOPMed
gnomAD
CA7523332
rs754376278
398 A>P No ClinGen
ExAC
gnomAD
rs1595467782
CA392100097
402 V>A No ClinGen
Ensembl
CA7523330
rs755636366
404 R>I No ClinGen
ExAC
gnomAD
CA392100007
rs1195163608
405 S>R No ClinGen
TOPMed
gnomAD
rs752082508
CA7523329
406 P>Q No ClinGen
ExAC
gnomAD
rs759097117
CA7523327
407 G>D No ClinGen
ExAC
gnomAD
CA7523328
rs145808054
407 G>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs772079307
CA7523298
409 V>I No ClinGen
ExAC
gnomAD
CA392098388
rs1412093546
410 H>P No ClinGen
TOPMed
gnomAD
rs1041720675
CA269974140
410 H>Q No ClinGen
Ensembl
CA392098340
rs1191644780
412 G>V No ClinGen
gnomAD
CA7523297
rs745915469
413 Y>C No ClinGen
ExAC
TOPMed
gnomAD
CA392098219
rs1179249544
420 L>V No ClinGen
gnomAD
CA392098191
rs1358758715
421 A>G No ClinGen
gnomAD
rs1210459216
CA392098202
421 A>T No ClinGen
gnomAD
CA7523295
rs771075009
422 I>V No ClinGen
ExAC
TOPMed
gnomAD
CA7523294
rs749722206
424 S>N No ClinGen
ExAC
gnomAD
CA392098097
rs1350619323
425 E>D No ClinGen
TOPMed
CA392098106
rs1274292869
425 E>K No ClinGen
TOPMed
rs369554008
CA7523292
426 T>N No ClinGen
ESP
ExAC
gnomAD
TCGA novel 429 Y>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs781695131
CA7523290
432 L>F No ClinGen
ExAC
gnomAD
rs1203716081
CA392097919
432 L>P No ClinGen
TOPMed
rs781695131
CA392097931
432 L>V No ClinGen
ExAC
gnomAD
CA7523288
rs751019557
433 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs754467254
CA7523289
433 R>W No ClinGen
ExAC
TOPMed
gnomAD
rs1420128202
CA392097865
434 N>K No ClinGen
gnomAD
CA392097847
rs1381900513
435 C>R No ClinGen
gnomAD
CA7523286
rs758116202
436 H>Q No ClinGen
ExAC
gnomAD
rs750297466
CA7523285
437 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA392097722
rs1255761033
440 Q>K No ClinGen
TOPMed
CA7523284
rs764305921
441 L>P No ClinGen
ExAC
gnomAD
CA392097700
rs1595466980
441 L>V No ClinGen
Ensembl
rs1203252723
CA392097652
443 G>* No ClinGen
gnomAD
rs1451578696
CA392097626
444 A>E No ClinGen
TOPMed
CA7523281
rs753745948
444 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs1451578696
CA392097620
444 A>V No ClinGen
TOPMed
rs1354921709
CA392097578
COSM1493437
447 E>K kidney Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
CA7523280
rs146772052
448 R>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA392097526
rs1595466957
449 L>V No ClinGen
Ensembl
rs1245463763
CA392097490
450 W>* No ClinGen
gnomAD
rs1320988913
CA392097470
451 E>G No ClinGen
gnomAD
rs576666978
CA7523279
453 G>D No ClinGen
ExAC
TOPMed
gnomAD
CA269973978
rs79105877
455 L>F No ClinGen
gnomAD
rs1297240432
CA392097395
455 L>R No ClinGen
gnomAD
rs79105877
CA392097402
455 L>V No ClinGen
gnomAD
rs202186966
CA7523278
457 T>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7523276
rs771201858
460 Q>E No ClinGen
ExAC
gnomAD
rs1025700275
CA269973921
462 R>Q No ClinGen
TOPMed
gnomAD
rs142610145
CA7523275
462 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA392097241
rs1333521234
463 T>N No ClinGen
TOPMed
CA392097232
rs1566882810
464 K>E No ClinGen
Ensembl
CA392097180
rs1237499131
466 K>T No ClinGen
TOPMed
rs1479078547
CA392097097
469 Q>H No ClinGen
gnomAD
CA7523273
rs770086195
470 T>I No ClinGen
ExAC
gnomAD
rs1192976856
CA392097038
473 R>Q No ClinGen
TOPMed
gnomAD
rs369750925
COSM167540
CA269973896
473 R>W Variant assessed as Somatic; 0.0 impact. large_intestine endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ESP
NCI-TCGA
TOPMed
gnomAD
TCGA novel 476 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA7523270
rs769137066
480 A>T No ClinGen
ExAC
gnomAD
CA392096880
rs1280013037
481 P>L No ClinGen
gnomAD
CA392096703
rs1316549759
490 M>V No ClinGen
gnomAD
CA269973815
rs939213299
491 D>H No ClinGen
TOPMed
gnomAD
CA7523267
rs758167367
492 A>T No ClinGen
ExAC
gnomAD
TCGA novel 493 L>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs750133880
CA7523266
494 V>L No ClinGen
ExAC
TOPMed
gnomAD
rs750133880
CA269973801
494 V>M No ClinGen
ExAC
TOPMed
gnomAD
rs946353904
CA269973800
495 S>I No ClinGen
TOPMed
gnomAD
rs757019551
CA7523264
497 R>Q No ClinGen
ExAC
TOPMed
gnomAD
CA7523265
rs778664376
497 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs753603052
CA7523263
498 V>I No ClinGen
ExAC
gnomAD
TCGA novel 499 A>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA392096551
rs1422759036
500 A>S No ClinGen
gnomAD
CA392096533
rs1478184493
501 P>R No ClinGen
gnomAD
CA7523262
rs201009870
501 P>S No ClinGen
1000Genomes
ExAC
gnomAD
CA269973790
rs201009870
501 P>T No ClinGen
1000Genomes
ExAC
gnomAD
CA392096514
rs1453500849
503 N>D No ClinGen
TOPMed
CA7523261
rs147749773
503 N>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7523260
rs377268526
504 D>H No ClinGen
ESP
ExAC
gnomAD
rs377268526
CA392096494
504 D>N No ClinGen
ESP
ExAC
gnomAD
rs766414519
CA7523259
505 G>C No ClinGen
ExAC
TOPMed
gnomAD
rs3917222
CA269973767
506 Q>L No ClinGen
Ensembl
CA7523257
rs201902651
508 E>D No ClinGen
1000Genomes
ExAC
gnomAD
rs762977866
CA392096424
508 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs762977866
CA7523258
508 E>Q No ClinGen
ExAC
TOPMed
gnomAD
rs769999057
CA7523256
509 T>I No ClinGen
ExAC
TOPMed
gnomAD
rs769999057
CA392096401
509 T>S No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 510 A>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1257906463
CA392096385
510 A>V No ClinGen
gnomAD
CA392096361
rs1198799110
512 C>Y No ClinGen
gnomAD
TCGA novel 513 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 513 P>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs145699954
CA7523254
514 V>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA392096324
rs1293543839
515 Q>* No ClinGen
TOPMed
gnomAD
rs1293543839
CA392096322
515 Q>E No ClinGen
TOPMed
gnomAD
CA392096305
CA7523253
rs769098912
516 G>R No ClinGen
ExAC
gnomAD
rs747492950
CA7523252
517 T>P No ClinGen
ExAC
TOPMed
gnomAD
rs780669763
CA7523251
518 S>G No ClinGen
ExAC
TOPMed
gnomAD
rs750350792
CA269973720
520 A>S No ClinGen
ExAC
TOPMed
gnomAD
rs750350792
CA7523250
520 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs1331936692
CA392096205
522 A>P No ClinGen
gnomAD
rs745319191
CA7523249
522 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA7523248
rs778438562
523 Q>R No ClinGen
ExAC
gnomAD
rs756930650
CA7523247
524 K>R No ClinGen
ExAC
gnomAD
rs1348713021
CA392096159
525 Q>K No ClinGen
gnomAD
rs1479695351
CA392096131
526 A>G No ClinGen
TOPMed
rs749095806
CA7523246
528 E>K No ClinGen
ExAC
gnomAD
rs139243405
CA7523245
529 A>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7523243
rs371535992
531 E>K No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs767392497
CA7523242
532 A>D No ClinGen
ExAC
gnomAD
rs767392497
CA392096032
532 A>G No ClinGen
ExAC
gnomAD
CA269973659
rs532162092
532 A>S No ClinGen
1000Genomes
CA392096008
rs1179793898
534 E>Q No ClinGen
gnomAD
rs758485935
CA7523241
535 E>K No ClinGen
ExAC
gnomAD
rs750431845
CA7523240
536 D>G No ClinGen
ExAC
gnomAD
CA269973652
rs984379697
538 D>G No ClinGen
TOPMed
gnomAD
rs560406082
CA7523237
541 E>D No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs761663803
CA7523238
541 E>G No ClinGen
ExAC
TOPMed
gnomAD
rs1370991669
CA392095817
544 T>I No ClinGen
TOPMed
rs1365343763
CA392095813
545 E>Q No ClinGen
TOPMed
gnomAD
CA269973639
rs370272155
546 I>T No ClinGen
gnomAD
CA7523234
rs761074357
547 P>A No ClinGen
ExAC
gnomAD
rs201083890
CA269973628
547 P>L No ClinGen
TOPMed
rs201083890
CA392095771
547 P>R No ClinGen
TOPMed
rs1268168245
CA392095760
548 P>Q No ClinGen
gnomAD
rs772644607
CA7523232
549 G>R No ClinGen
ExAC
TOPMed
gnomAD
CA392095725
rs1373630465
551 V>I No ClinGen
TOPMed
rs773899606
CA7523229
554 R>H No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 555 A>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs770540121
CA7523228
558 L>S No ClinGen
ExAC
gnomAD
CA392095592
rs1463178482
560 Q>* No ClinGen
Ensembl
rs1035798249
CA269973553
561 S>R No ClinGen
TOPMed
rs148746894
CA269973551
562 P>L No ClinGen
ESP
TOPMed
gnomAD
rs1265819008
CA392095553
562 P>S No ClinGen
gnomAD
rs143986040
CA7523226
563 R>C No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7523225
rs755923103
563 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
CA392094150
rs1333746566
564 G>V No ClinGen
TOPMed
rs142581706
CA7523208
568 G>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs368938451
CA7523206
570 E>D No ClinGen
1000Genomes
ESP
ExAC
gnomAD
rs1595465842
CA392094095
570 E>G No ClinGen
Ensembl
rs549066454
CA392094097
570 E>K No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7523207
rs549066454
570 E>Q No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7523205
rs769369588
571 N>K No ClinGen
ExAC
gnomAD
CA392094075
rs1216819260
573 D>N No ClinGen
gnomAD
rs748000591
CA7523204
574 N>D No ClinGen
ExAC
gnomAD
CA7523203
rs375945705
576 K>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1037149140
CA269971862
576 K>R No ClinGen
gnomAD
rs888510264
CA269971857
577 R>Q No ClinGen
TOPMed
gnomAD
rs545133458
CA7523202
577 R>W No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs764178423
CA7523201
578 D>G No ClinGen
ExAC
TOPMed
gnomAD
rs1467022255
CA392094035
578 D>H No ClinGen
gnomAD
TCGA novel 578 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs371680057
CA7523200
583 V>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA392093963
rs1200496716
586 H>R No ClinGen
TOPMed
rs757374709
CA7523199
587 R>G No ClinGen
ExAC
gnomAD
rs138731321
CA7523198
587 R>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA269971812
rs921257955
587 R>T No ClinGen
TOPMed
CA392093944
rs1421879518
589 L>V No ClinGen
gnomAD
CA7523197
rs200716301
590 L>P No ClinGen
1000Genomes
ExAC
gnomAD
CA7523196
rs756391602
591 A>T No ClinGen
ExAC
gnomAD
CA392093925
rs1595465804
591 A>V No ClinGen
Ensembl
CA392093916
rs1462612196
592 R>I No ClinGen
gnomAD
CA392093911
rs1256006409
593 S>P No ClinGen
gnomAD
CA392093907
rs1595465801
593 S>Y No ClinGen
Ensembl
rs1317347777
CA392093894
595 R>G No ClinGen
gnomAD
CA392093891
rs1269036018
595 R>T No ClinGen
TOPMed
rs146267149
CA7523195
596 K>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1192336467
CA392093866
598 P>L No ClinGen
TOPMed
TCGA novel 599 R>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs141880595
CA7523193
599 R>P No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
COSM109671
CA7523192
rs141880595
599 R>Q liver skin [Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs192532525
CA7523194
599 R>W No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA392093851
rs1312473699
600 Y>C No ClinGen
gnomAD
rs1396906518
CA392093821
602 H>Y No ClinGen
gnomAD
rs572072217
CA7523190
603 Q>* No ClinGen
1000Genomes
ExAC
gnomAD
rs1464693922
CA392093803
603 Q>R No ClinGen
TOPMed
gnomAD
rs1400355489
CA392093792
604 G>S No ClinGen
gnomAD
TCGA novel 606 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs772593046
CA7523189
607 N>D No ClinGen
ExAC
gnomAD
CA7523188
rs138379738
607 N>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs776448467
CA7523186
608 E>G No ClinGen
ExAC
gnomAD
CA7523187
rs368170187
608 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1566881939
CA392093703
609 S>N No ClinGen
Ensembl
rs768468072
CA7523185
611 C>Y No ClinGen
ExAC
TOPMed
gnomAD
rs780048155
CA7523183
612 R>K No ClinGen
ExAC
gnomAD
rs1458125014
CA392093638
613 S>* No ClinGen
gnomAD
rs771903211
CA7523182
614 G>E No ClinGen
ExAC
gnomAD
CA392093606
rs1405590589
615 R>T No ClinGen
TOPMed
TCGA novel 618 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA392093541
rs1297624535
619 K>M No ClinGen
TOPMed
CA392093498
rs1566881929
622 G>R No ClinGen
Ensembl
CA392093481
rs150098604
623 E>* Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
CA7523179
rs150098604
623 E>K No ClinGen
ESP
ExAC
TOPMed
CA392093476
rs1296212688
623 E>V No ClinGen
TOPMed
TCGA novel 624 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1307769720
CA392093395
628 L>M No ClinGen
TOPMed
gnomAD
rs752609459
CA269971729
630 L>I No ClinGen
Ensembl
CA7523175
rs753000031
630 L>P No ClinGen
ExAC
gnomAD
rs781517782
CA7523174
631 P>L No ClinGen
ExAC
TOPMed
gnomAD
rs201391518
CA7523172
632 E>G No ClinGen
1000Genomes
ExAC
rs1566881908
CA392093326
635 L>F No ClinGen
Ensembl
CA269971715
rs924983824
638 V>I No ClinGen
Ensembl
rs908482454
CA392093215
643 R>K No ClinGen
TOPMed
gnomAD
CA269971713
rs908482454
643 R>T No ClinGen
TOPMed
gnomAD
CA7523171
rs766976345
647 G>R No ClinGen
ExAC
gnomAD
CA7523170
rs763351789
649 R>S No ClinGen
ExAC
gnomAD
CA7523169
rs749981326
650 P>S No ClinGen
ExAC
gnomAD
rs867793790
CA269971683
651 Y>H No ClinGen
Ensembl
CA392093054
rs1297883135
652 K>I No ClinGen
TOPMed
CA392093056
rs1297883135
652 K>R No ClinGen
TOPMed
CA392093032
rs776281990
653 Y>* No ClinGen
ExAC
gnomAD
CA7523167
rs148013567
653 Y>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7523165
rs763672739
654 L>P No ClinGen
ExAC
gnomAD
rs1449925232
CA392092965
656 Y>C No ClinGen
gnomAD
TCGA novel 657 S>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs142885180
CA7523163
660 F>C No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA392092826
rs1223465627
662 P>L No ClinGen
gnomAD
rs772096076
CA7523162
663 N>K No ClinGen
ExAC
gnomAD
CA7523160
rs537398238
665 L>F No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7523159
rs537398238
665 L>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1352041777
CA392092744
667 M>L No ClinGen
gnomAD
CA7523157
rs781568758
669 Q>H No ClinGen
ExAC
TOPMed
gnomAD
CA392092684
rs1230515260
670 V>I No ClinGen
TOPMed
gnomAD
CA392092660
rs1329967614
671 S>F Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA7523156
rs374146791
672 H>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7523155
rs780255136
673 Q>* No ClinGen
ExAC
gnomAD
rs780255136
CA7523154
673 Q>K No ClinGen
ExAC
gnomAD
CA392092619
rs1238965962
673 Q>R No ClinGen
TOPMed
CA7523153
rs758980263
674 V>L No ClinGen
ExAC
TOPMed
gnomAD
CA392092607
rs758980263
674 V>M No ClinGen
ExAC
TOPMed
gnomAD
CA392092553
rs1420076800
676 N>K No ClinGen
gnomAD
rs1297358846
CA392092559
676 N>S No ClinGen
gnomAD
CA392092529
rs1410145814
678 Y>H No ClinGen
gnomAD
CA392092506
rs1170720105
679 K>E No ClinGen
gnomAD
rs765681915
CA7523151
679 K>N No ClinGen
ExAC
gnomAD
rs750956069
CA7523152
679 K>R No ClinGen
ExAC
gnomAD
CA392092477
rs1355159490
680 C>Y No ClinGen
TOPMed
rs1243161381
CA392092407
683 C>* No ClinGen
TOPMed
CA7523149
rs571452426
683 C>S No ClinGen
1000Genomes
ExAC
gnomAD
CA7523148
rs763869282
683 C>Y No ClinGen
ExAC
gnomAD
rs1216435229
CA392092380
685 K>E No ClinGen
gnomAD
CA269971596
rs868055140
688 S>N No ClinGen
Ensembl
CA7523146
rs557989661
689 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7523147
rs760226206
689 R>W No ClinGen
ExAC
TOPMed
gnomAD
rs534618732
CA392092289
690 S>G No ClinGen
1000Genomes
ExAC
gnomAD
rs759328165
CA392092271
CA7523144
690 S>R No ClinGen
ExAC
gnomAD
CA7523145
rs534618732
690 S>R No ClinGen
1000Genomes
ExAC
gnomAD
rs1283378978
CA392092249
692 R>* No ClinGen
TOPMed
gnomAD
CA7523143
rs774446390
692 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs748304231
CA7523141
693 L>F No ClinGen
ExAC
gnomAD
CA7523139
rs138662722
694 I>N No ClinGen
1000Genomes
ExAC
gnomAD
CA7523140
rs138662722
694 I>S No ClinGen
1000Genomes
ExAC
gnomAD
CA7523136
rs747165159
696 H>D No ClinGen
ExAC
gnomAD
CA392092159
rs1464699751
696 H>P No ClinGen
gnomAD
rs140834077
CA7523134
697 R>Q No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA7523135
rs144818669
697 R>W No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA392092131
rs1481458724
698 R>G No ClinGen
gnomAD
CA7523133
rs746167303
698 R>K No ClinGen
ExAC
gnomAD
CA392092066
rs1193195066
701 T>A No ClinGen
TOPMed
gnomAD
rs200617858
CA269971512
701 T>I No ClinGen
ExAC
gnomAD
CA7523132
rs200617858
701 T>S No ClinGen
ExAC
gnomAD
rs1244213597
CA392092042
703 E>K No ClinGen
TOPMed
gnomAD
CA392092040
rs1244213597
703 E>Q No ClinGen
TOPMed
gnomAD
CA392092031
rs1208382356
703 E>V No ClinGen
gnomAD
rs757751770
CA7523131
704 K>E No ClinGen
ExAC
gnomAD
rs1264296789
CA392091990
705 P>R No ClinGen
gnomAD
CA7523130
rs371950140
706 Y>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 707 K>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1214829963
CA392091911
710 D>H No ClinGen
gnomAD
TCGA novel 713 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1029029875
CA269971499
714 S>T No ClinGen
TOPMed
rs755610316
CA7523128
716 R>C No ClinGen
ExAC
TOPMed
gnomAD
CA7523127
rs368532710
716 R>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 717 D>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA269971483
rs374579190
720 N>D No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs759407427
CA7523125
720 N>T No ClinGen
ExAC
TOPMed
gnomAD
CA7523126
rs374579190
720 N>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA392091621
rs1471027481
725 R>K No ClinGen
gnomAD
TCGA novel 725 R>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 726 R>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA392091606
rs1566881752
726 R>K No ClinGen
Ensembl
CA392091581
rs1342361445
728 H>N No ClinGen
gnomAD
CA392091553
rs1410756533
730 G>R No ClinGen
gnomAD
CA392091510
rs762961093
733 P>L No ClinGen
ExAC
TOPMed
gnomAD
rs762961093
CA7523121
733 P>R No ClinGen
ExAC
TOPMed
gnomAD
CA392091515
rs1276166034
733 P>S No ClinGen
TOPMed
gnomAD
rs776807655
CA7523120
737 G>S No ClinGen
ExAC
gnomAD
CA392091439
rs1244346801
737 G>V No ClinGen
gnomAD
rs868086848
CA269971443
738 E>D No ClinGen
gnomAD
CA7523119
rs768645431
738 E>V No ClinGen
ExAC
gnomAD
CA7523118
rs187725072
739 C>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs944031359
CA269971442
740 G>E No ClinGen
gnomAD
CA392091326
rs1227593639
744 N>S No ClinGen
gnomAD
CA392091313
rs1296111851
745 Q>* No ClinGen
TOPMed
gnomAD
CA392091317
rs1296111851
745 Q>K No ClinGen
TOPMed
gnomAD
CA392091284
rs1412835836
748 S>I No ClinGen
TOPMed
CA7523116
rs772337108
748 S>R No ClinGen
ExAC
gnomAD
rs1317130905
CA392091289
748 S>R No ClinGen
gnomAD
TCGA novel 749 L>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 750 I>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs746292251
CA7523115
751 I>N No ClinGen
ExAC
TOPMed
gnomAD
rs749825808
CA7523113
753 Q>H No ClinGen
ExAC
TOPMed
gnomAD
CA7523114
rs779231401
753 Q>R No ClinGen
ExAC
CA392091238
rs1424472047
755 T>N No ClinGen
gnomAD
rs1386282500
CA392091222
757 T>I No ClinGen
gnomAD
TCGA novel 758 G>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA392091203
rs1438400871
760 K>R No ClinGen
gnomAD
rs1402258921
CA392091199
761 P>T No ClinGen
TOPMed
rs1566881680
CA392091190
762 Y>C No ClinGen
Ensembl
CA7523111
rs201501335
762 Y>H No ClinGen
ExAC
TOPMed
gnomAD
rs755594702
CA7523110
763 Q>* No ClinGen
ExAC
gnomAD
rs1244673966
CA392091166
765 E>V No ClinGen
TOPMed
gnomAD
rs200216810
CA269971358
766 E>G No ClinGen
1000Genomes
rs559211825
CA7523108
767 C>Y No ClinGen
ExAC
TOPMed
gnomAD
CA392091139
rs1293685955
769 K>R No ClinGen
gnomAD
rs751448544
CA7523106
771 F>S No ClinGen
ExAC
gnomAD
CA7523107
rs754663565
771 F>V No ClinGen
ExAC
TOPMed
gnomAD
CA7523104
rs762792714
772 N>S No ClinGen
ExAC
TOPMed
gnomAD
rs1394523590
CA392091108
773 N>K No ClinGen
gnomAD
rs1256542554
CA392091105
774 S>G No ClinGen
TOPMed
rs765195394
CA7523103
774 S>I No ClinGen
ExAC
gnomAD
rs765163078
CA7523102
775 S>P No ClinGen
ExAC
rs1291819288
CA392091092
776 H>Y No ClinGen
gnomAD
CA392091085
rs1366366330
777 F>L No ClinGen
gnomAD
CA269971295
rs146581346
778 S>N No ClinGen
ESP
TOPMed
gnomAD
rs775627654
CA7523100
779 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA7523099
rs376118926
780 H>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA7523096
rs771311895
781 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA7523097
rs774520763
781 R>W No ClinGen
ExAC
gnomAD
rs749599822
CA7523095
782 R>K No ClinGen
ExAC
TOPMed
gnomAD
CA7523094
rs778150222
783 I>T No ClinGen
ExAC
TOPMed
gnomAD
rs747666309
CA7523092
785 T>R No ClinGen
ExAC
gnomAD
CA392091028
rs1429244183
786 G>E No ClinGen
gnomAD
TCGA novel 789 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs144329084
CA392091001
790 H>P No ClinGen
1000Genomes
ESP
ExAC
TOPMed
CA7523090
rs144329084
790 H>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
CA269971187
rs967575936
791 V>M No ClinGen
TOPMed
CA7523088
rs751287294
792 C>R No ClinGen
ExAC
TOPMed
gnomAD
rs202117016
CA269971169
793 P>L No ClinGen
1000Genomes
rs1566881613
CA392090983
793 P>S No ClinGen
Ensembl
CA392090979
rs1222911805
794 D>Y No ClinGen
gnomAD
TCGA novel 795 C>W Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA269971156
rs912098583
798 S>C No ClinGen
TOPMed
gnomAD
CA7523087
rs199524651
798 S>N No ClinGen
ExAC
TOPMed
gnomAD
rs1384664848
CA392090926
801 K>* No ClinGen
gnomAD
rs1384664848
CA392090927
801 K>E No ClinGen
gnomAD
CA269971137
rs1027546393
805 L>S No ClinGen
Ensembl
CA7523085
rs139281371
806 R>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs146256400
CA7523084
806 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA392090876
rs1186491707
808 H>Q No ClinGen
gnomAD
rs765148236
CA7523083
808 H>R No ClinGen
ExAC
gnomAD
rs1019713475
CA269971093
809 H>R No ClinGen
TOPMed
CA392090873
rs1480469246
809 H>Y Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs752761161
CA7523081
810 R>G No ClinGen
ExAC
gnomAD
CA7523079
rs759568097
813 T>I No ClinGen
ExAC
CA7523080
rs767615218
813 T>S No ClinGen
ExAC
gnomAD
rs183729618
CA7523078
814 G>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs148692928
CA7523076
815 E>K No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7523077
rs148692928
815 E>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA7523073
rs577733957
817 P>L No ClinGen
1000Genomes
ExAC
gnomAD
CA7523074
rs770249788
817 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs777234394
CA7523072
818 Y>C No ClinGen
ExAC
gnomAD
TCGA novel 818 Y>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs866743360
CA269970993
819 G>E No ClinGen
Ensembl
rs746459746
CA7523070
821 H>D No ClinGen
ExAC
TOPMed
gnomAD
CA269970982
rs936554556
821 H>R No ClinGen
Ensembl
CA392090783
rs1162399784
823 C>Y No ClinGen
TOPMed
rs779855498
CA7523069
824 G>D No ClinGen
ExAC
gnomAD
CA392090770
rs1411418252
825 K>R No ClinGen
TOPMed
CA7523068
rs758112106
827 F>S No ClinGen
ExAC
gnomAD
CA392090738
rs866291185
828 S>I No ClinGen
gnomAD
rs866291185
CA269970973
828 S>N No ClinGen
gnomAD
rs1566881545
CA392090713
830 S>G No ClinGen
Ensembl
CA7523067
rs745700387
832 A>S No ClinGen
ExAC
gnomAD
TCGA novel 832 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs756962367
CA7523065
833 L>F No ClinGen
ExAC
gnomAD
TCGA novel 835 K>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs35278805
CA392090623
836 H>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA392090613
rs1359268042
837 G>A No ClinGen
TOPMed
rs149461798
CA7523063
837 G>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA392090604
rs1172341777
838 E>G No ClinGen
gnomAD
CA7523062
rs755058248
838 E>Q No ClinGen
ExAC
gnomAD
rs751637493
CA7523061
840 H>D No ClinGen
ExAC
gnomAD
rs766644002
CA7523060
840 H>R No ClinGen
ExAC
gnomAD
CA7523057
rs137944091
842 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs202173229
CA7523058
842 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1328741607
CA392090524
844 K>* No ClinGen
TOPMed
rs940480583
CA269970911
844 K>N No ClinGen
Ensembl
CA7523056
rs762034528
845 L>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs370490171
CA269970901
847 T>I No ClinGen
ESP
TOPMed
gnomAD
CA392090484
rs370490171
847 T>K No ClinGen
ESP
TOPMed
gnomAD
CA392090478
rs1230129270
848 Q>* No ClinGen
TOPMed
gnomAD
rs187742338
CA7523055
849 S>* No ClinGen
1000Genomes
ExAC
gnomAD
CA7523054
rs769218009
851 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA269970880
rs1055360301
852 K>R No ClinGen
TOPMed
rs746583185
CA7523053
853 K>Q No ClinGen
ExAC
gnomAD
rs775119312
CA7523052
853 K>S No ClinGen
ExAC
TOPMed
gnomAD

No associated diseases with Q8IWY8

9 regional properties for Q8IWY8

Type Name Position InterPro Accession
domain SCAN domain 14 - 126 IPR003309
domain Zinc finger C2H2-type 678 - 705 IPR013087-1
domain Zinc finger C2H2-type 706 - 733 IPR013087-2
domain Zinc finger C2H2-type 734 - 761 IPR013087-3
domain Zinc finger C2H2-type 762 - 789 IPR013087-4
domain Zinc finger C2H2-type 790 - 817 IPR013087-5
domain Zinc finger C2H2-type 818 - 845 IPR013087-6
domain Myb/SANT-like DNA-binding domain 4 246 - 330 IPR044822-1
domain Myb/SANT-like DNA-binding domain 4 409 - 493 IPR044822-2

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.

4 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.
sequence-specific double-stranded DNA binding Binding to double-stranded 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.

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
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
Q63HK3 ZKSCAN2 Zinc finger protein with KRAB and SCAN domains 2 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
MMAKSALREN GTNSETFRQR FRRFHYQEVA GPREAFSQLW ELCCRWLRPE VRTKEQIVEL
70 80 90 100 110 120
LVLEQFLTVL PGEIQNWVQE QCPENGEEAV TLVEDLEREP GRPRSSVTVS VKGQEVRLEK
130 140 150 160 170 180
MTPPKSSQEL LSVRQESVEP QPRGVPKKER ARSPDLGPQE QMNPKEKLKP FQRSGLPFPK
190 200 210 220 230 240
SGVVSRLEQG EPWIPDLLGS KEKELPSGSH IGDRRVHADL LPSKKDRRSW VEQDHWSFED
250 260 270 280 290 300
EKVAGVHWGY EETRTLLAIL SQTEFYEALR NCHRNSQVYG AVAERLREYG FLRTLEQCRT
310 320 330 340 350 360
KFKGLQKSYR KVKSGHPPET CPFFEEMEAL MSAQVIALPS NGLEAAASHS GLVGSDAETE
370 380 390 400 410 420
EPGQRGWQHE EGAEEAVAQE SDSDDMDLEA TPQDPNSAAP VVFRSPGGVH WGYEETKTYL
430 440 450 460 470 480
AILSETQFYE ALRNCHRNSQ LYGAVAERLW EYGFLRTPEQ CRTKFKSLQT SYRKVKNGQA
490 500 510 520 530 540
PETCPFFEEM DALVSVRVAA PPNDGQEETA SCPVQGTSEA EAQKQAEEAD EATEEDSDDD
550 560 570 580 590 600
EEDTEIPPGA VITRAPVLFQ SPRGFEAGFE NEDNSKRDIS EEVQLHRTLL ARSERKIPRY
610 620 630 640 650 660
LHQGKGNESD CRSGRQWAKT SGEKRGKLTL PEKSLSEVLS QQRPCLGERP YKYLKYSKSF
670 680 690 700 710 720
GPNSLLMHQV SHQVENPYKC ADCGKSFSRS ARLIRHRRIH TGEKPYKCLD CGKSFRDSSN
730 740 750 760 770 780
FITHRRIHTG EKPYQCGECG KCFNQSSSLI IHQRTHTGEK PYQCEECGKS FNNSSHFSAH
790 800 810 820 830 840
RRIHTGERPH VCPDCGKSFS KSSDLRAHHR THTGEKPYGC HDCGKCFSKS SALNKHGEIH
850
AREKLLTQSA PK