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 Q14526

Entry ID Method Resolution Chain Position Source
AF-Q14526-F1 Predicted AlphaFoldDB

599 variants for Q14526

Variant ID(s) Position Change Description Diseaes Association Provenance
TCGA novel 1 M>? Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8277705
rs759227632
2 T>I No ClinGen
ExAC
TOPMed
gnomAD
CA397608323
rs1481933957
4 P>S No ClinGen
gnomAD
CA397608330
rs1218143585
5 E>K No ClinGen
TOPMed
CA286891042
rs865795282
6 A>E No ClinGen
Ensembl
rs375835534
CA8277706
7 D>V No ClinGen
ESP
ExAC
gnomAD
rs755570032
CA8277708
8 I>F No ClinGen
ExAC
gnomAD
rs755570032
CA397608359
8 I>V No ClinGen
ExAC
gnomAD
rs201780325
CA8277709
9 L>F No ClinGen
ExAC
TOPMed
gnomAD
CA286891049
rs538995868
10 L>F No ClinGen
TOPMed
gnomAD
CA8277710
rs377629449
12 S>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs376178946
CA8277711
12 S>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA397608413
rs1463493787
13 G>R No ClinGen
gnomAD
CA286891170
rs988953921
14 E>D No ClinGen
TOPMed
gnomAD
rs1486315140
CA397609824
14 E>K No ClinGen
gnomAD
CA286891172
rs914732446
16 A>G No ClinGen
Ensembl
rs867961680
CA286891174
17 G>V No ClinGen
Ensembl
rs369608521
CA8277736
18 Q>* No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA397609885
rs1323556947
19 T>A No ClinGen
TOPMed
CA8277737
rs770371287
19 T>K No ClinGen
ExAC
TOPMed
gnomAD
CA8277738
rs778413153
21 L>P No ClinGen
ExAC
TOPMed
gnomAD
rs1597301572
CA397609930
22 D>E No ClinGen
Ensembl
rs749739446
CA8277739
22 D>N No ClinGen
ExAC
TOPMed
gnomAD
CA397609939
rs1567556205
23 T>M No ClinGen
Ensembl
rs1400206993
CA397609934
23 T>P No ClinGen
gnomAD
rs768515787
CA8277740
26 A>S No ClinGen
ExAC
TOPMed
gnomAD
CA397609987
rs1567556211
27 P>A No ClinGen
Ensembl
CA397609990
rs1285242739
27 P>R No ClinGen
gnomAD
rs1021443642
CA397609997
28 G>C No ClinGen
TOPMed
gnomAD
CA286891185
rs1021443642
28 G>S No ClinGen
TOPMed
gnomAD
CA397610007
rs1286416765
29 H>Y No ClinGen
gnomAD
CA397610037
rs775228381
31 R>S No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 33 L>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1597301612
CA397610054
33 L>V No ClinGen
Ensembl
rs775944925
CA8277744
36 Q>R No ClinGen
ExAC
gnomAD
CA397610108
rs1469557052
38 N>D No ClinGen
gnomAD
rs1175029400
CA397610115
38 N>S No ClinGen
gnomAD
CA397610122
rs1409496536
39 N>H No ClinGen
gnomAD
CA8277746
rs765223557
49 V>A No ClinGen
ExAC
gnomAD
CA397610221
rs1418807822
52 V>M No ClinGen
TOPMed
rs1335749666
CA397610251
56 A>S No ClinGen
gnomAD
CA8277749
rs200866682
56 A>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs751838541
CA8277750
57 L>V No ClinGen
ExAC
gnomAD
CA397610346
rs1597301682
64 V>M No ClinGen
Ensembl
CA397610443
rs1178481585
70 A>G No ClinGen
gnomAD
CA397610463
rs1439715958
72 L>F No ClinGen
gnomAD
rs1003950764
CA286891201
74 S>Y No ClinGen
TOPMed
rs1212291603
CA397610525
76 V>L No ClinGen
TOPMed
rs779076274
CA8277758
78 H>D No ClinGen
ExAC
TOPMed
gnomAD
rs779076274
CA397610551
78 H>Y No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 81 L>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 84 L>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1401140755
CA397610659
85 D>E No ClinGen
gnomAD
CA8277761
rs776342843
85 D>G No ClinGen
ExAC
gnomAD
rs1466164005
CA397610698
88 M>L No ClinGen
TOPMed
gnomAD
CA8277762
rs375891653
89 V>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs769269916
CA8277763
90 S>C No ClinGen
ExAC
gnomAD
CA286891212
rs959379377
90 S>N No ClinGen
TOPMed
TCGA novel 91 P>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs762840071
CA8277765
95 R>H No ClinGen
ExAC
gnomAD
CA397610798
rs1338454162
101 I>V No ClinGen
gnomAD
rs867944680
CA286891219
104 G>S No ClinGen
Ensembl
CA8277768
rs759366814
COSM3691417
COSM3691418
105 R>C Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA397610832
rs1212587447
105 R>H No ClinGen
gnomAD
CA8277769
rs767700597
107 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA8277770
rs752940567
108 D>E No ClinGen
ExAC
TOPMed
gnomAD
rs1199079684
CA397610879
109 G>D No ClinGen
gnomAD
rs756281134
CA8277771
110 A>S No ClinGen
ExAC
gnomAD
rs1030020126
CA286891235
112 A>T No ClinGen
Ensembl
rs1173462006
CA397610918
112 A>V No ClinGen
gnomAD
rs1461362736
CA397610919
113 A>T No ClinGen
TOPMed
gnomAD
CA397610932
rs1396742495
114 A>V No ClinGen
gnomAD
rs1387590285
CA397610947
115 A>V No ClinGen
gnomAD
CA397610951
rs1325649654
116 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs757644437
CA8277775
116 A>V No ClinGen
ExAC
rs1318583081
CA397610980
118 V>A Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA397610976
rs779461004
118 V>L No ClinGen
ExAC
gnomAD
CA8277776
rs779461004
118 V>M No ClinGen
ExAC
gnomAD
rs776247727
CA286891246
119 A>T No ClinGen
Ensembl
rs746282560
CA8277777
119 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA397611000
rs1259421390
120 P>S No ClinGen
gnomAD
CA397611022
rs1357790289
122 A>P No ClinGen
TOPMed
gnomAD
rs1357790289
CA397611024
122 A>S No ClinGen
TOPMed
gnomAD
rs1357790289
CA397611021
122 A>T No ClinGen
TOPMed
gnomAD
CA397611044
rs1210076297
124 P>S No ClinGen
gnomAD
CA8277779
rs780755971
131 A>S No ClinGen
ExAC
gnomAD
CA286891257
rs868096216
131 A>V No ClinGen
Ensembl
rs867279568
CA286891261
132 A>T No ClinGen
gnomAD
CA397611094
rs1303096155
132 A>V No ClinGen
TOPMed
CA397611097
rs1370286179
133 A>D No ClinGen
gnomAD
rs867843142
CA286891265
133 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
CA286891269
rs868132987
134 S>R No ClinGen
gnomAD
CA8277782
rs772643992
134 S>T No ClinGen
ExAC
TOPMed
gnomAD
rs1158067992
CA397611115
136 L>M No ClinGen
gnomAD
rs866942500
CA286891271
137 Q>K No ClinGen
Ensembl
rs867587867
CA286891275
139 P>H No ClinGen
Ensembl
rs980305162
CA286891273
139 P>S No ClinGen
Ensembl
rs1402054828
CA397611138
140 D>N No ClinGen
gnomAD
rs866530040
CA286891281
141 L>I No ClinGen
Ensembl
CA397611161
rs1414115294
143 A>G No ClinGen
TOPMed
gnomAD
CA286891286
rs867149812
143 A>T No ClinGen
gnomAD
CA397611160
rs1414115294
143 A>V No ClinGen
TOPMed
gnomAD
CA397611162
rs1323002927
144 L>M No ClinGen
gnomAD
CA286891289
rs867560930
145 C>* No ClinGen
gnomAD
CA397611170
rs1244968750
145 C>Y No ClinGen
gnomAD
CA8277785
rs774343853
146 K>Q No ClinGen
ExAC
gnomAD
rs866185516
CA286891290
149 L>P No ClinGen
Ensembl
rs960340137
CA286891292
150 K>R No ClinGen
Ensembl
rs1287225276
CA397611209
151 R>C No ClinGen
gnomAD
rs1485518057
CA397611210
151 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA397611217
rs1258968912
152 H>L No ClinGen
gnomAD
rs918572711
CA286891296
153 G>A No ClinGen
TOPMed
rs918572711
CA397611224
153 G>D No ClinGen
TOPMed
rs1489857429
CA397611232
154 K>N No ClinGen
TOPMed
rs866896900
CA286891299
155 Y>* No ClinGen
Ensembl
rs1293810774
CA397611242
156 C>R No ClinGen
TOPMed
rs945519529
CA286891300
156 C>Y No ClinGen
TOPMed
rs1181243385
CA397611252
157 H>N No ClinGen
gnomAD
CA397611270
rs1362105584
158 L>P No ClinGen
gnomAD
CA397611273
rs1421788874
159 R>W No ClinGen
gnomAD
CA397611281
rs1453540088
160 G>S No ClinGen
TOPMed
rs930001654
CA286891322
161 G>D No ClinGen
TOPMed
gnomAD
rs1343737291
CA397611295
161 G>S No ClinGen
TOPMed
rs1005212538
CA286891326
163 G>S No ClinGen
TOPMed
rs1406921584
CA397611354
167 G>S No ClinGen
TOPMed
gnomAD
rs1159422626
CA397611382
169 A>E No ClinGen
TOPMed
gnomAD
rs1344546752
CA397611379
169 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs1159422626
CA397611386
169 A>V No ClinGen
TOPMed
gnomAD
rs909999910
CA286891328
172 G>S No ClinGen
Ensembl
rs1300861331
CA397611439
175 G>D No ClinGen
gnomAD
CA397611449
rs1396510111
176 R>Q No ClinGen
gnomAD
rs1240083596
CA397611457
177 G>D No ClinGen
TOPMed
CA397611454
rs1305718105
177 G>R No ClinGen
TOPMed
gnomAD
rs966282867
CA286891332
181 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs974493544
CA286891336
182 T>A No ClinGen
TOPMed
CA397611572
rs1038869055
188 C>S No ClinGen
TOPMed
gnomAD
rs1038869055
CA286891341
188 C>Y No ClinGen
TOPMed
gnomAD
CA397611600
rs1209258018
190 P>L No ClinGen
TOPMed
gnomAD
CA397611599
rs1209258018
190 P>R No ClinGen
TOPMed
gnomAD
CA397611626
rs1483888191
193 V>F No ClinGen
TOPMed
gnomAD
rs775882169
CA8277793
196 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA286891347
rs997446732
197 P>L No ClinGen
TOPMed
CA397611716
rs1467802380
201 A>G No ClinGen
TOPMed
CA397611712
rs1452794932
201 A>S No ClinGen
gnomAD
rs1173749354
CA397611763
205 S>L No ClinGen
gnomAD
rs1417261564
CA397611811
210 A>S No ClinGen
TOPMed
rs1297486375
CA397611825
212 N>D No ClinGen
gnomAD
rs945609595
CA286891356
216 A>S No ClinGen
TOPMed
gnomAD
CA397611861
rs945609595
216 A>T No ClinGen
TOPMed
gnomAD
CA397611955
rs1217086504
220 A>E No ClinGen
TOPMed
gnomAD
TCGA novel 220 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1217086504
CA397611952
220 A>V No ClinGen
TOPMed
gnomAD
rs1303905181
CA397611965
221 S>A No ClinGen
gnomAD
rs1227358068
CA397611987
222 G>A No ClinGen
gnomAD
rs1227358068
CA397611984
222 G>E No ClinGen
gnomAD
rs750919684
CA8277799
222 G>R No ClinGen
ExAC
gnomAD
rs1227358068
CA397611990
222 G>V No ClinGen
gnomAD
rs1289614280
CA397612016
224 G>S No ClinGen
gnomAD
rs1199414678
CA397612042
225 P>L No ClinGen
gnomAD
CA8277800
rs758711363
225 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs755707715
CA8277803
228 A>T No ClinGen
ExAC
gnomAD
rs1433489374
CA397612108
229 L>F No ClinGen
TOPMed
gnomAD
rs1313928524
CA397612156
231 A>T No ClinGen
TOPMed
rs748867347
CA8277805
232 S>L No ClinGen
ExAC
TOPMed
gnomAD
rs939537964
CA286891378
233 E>G No ClinGen
TOPMed
rs1331488661
CA397612194
233 E>Q No ClinGen
gnomAD
rs1393047454
CA397612217
234 R>G No ClinGen
gnomAD
CA286891380
rs968501586
235 R>H Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
rs866319796
CA286891382
236 C>* No ClinGen
TOPMed
gnomAD
CA8277807
rs778769452
237 S>A No ClinGen
ExAC
TOPMed
gnomAD
CA397612265
rs778769452
237 S>P No ClinGen
ExAC
TOPMed
gnomAD
rs745774508
CA8277808
240 C>Y No ClinGen
ExAC
TOPMed
gnomAD
CA397612379
rs1382079308
242 L>Q No ClinGen
gnomAD
CA397612387
rs1276683798
243 D>N No ClinGen
gnomAD
CA397612408
rs1320680788
244 L>P No ClinGen
gnomAD
rs1219746423
CA397612482
248 S>N No ClinGen
gnomAD
CA397612498
rs1188300632
249 P>S No ClinGen
TOPMed
gnomAD
CA397612519
rs1332702601
250 P>L No ClinGen
TOPMed
gnomAD
CA286891392
rs895267158
250 P>S No ClinGen
TOPMed
gnomAD
CA397612534
rs1257084634
251 G>V No ClinGen
TOPMed
rs1567556697
CA397612564
253 A>T No ClinGen
Ensembl
CA397612583
rs1195344565
254 A>S No ClinGen
TOPMed
CA286891393
rs994792799
255 P>S No ClinGen
TOPMed
gnomAD
CA397612658
rs1049010510
258 P>L No ClinGen
TOPMed
gnomAD
rs1049010510
CA286891394
258 P>Q No ClinGen
TOPMed
gnomAD
CA397612674
rs1260731022
260 A>T No ClinGen
gnomAD
TCGA novel 261 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA397612726
rs1478782530
262 R>H No ClinGen
gnomAD
CA397612766
rs1034539312
265 P>H No ClinGen
TOPMed
rs1034539312
CA286891397
265 P>R No ClinGen
TOPMed
rs1359190275
CA397612762
265 P>S No ClinGen
TOPMed
CA286891398
rs960511203
266 P>R No ClinGen
Ensembl
CA397612796
rs886447137
267 R>C No ClinGen
TOPMed
gnomAD
rs886447137
CA286891400
267 R>S No ClinGen
TOPMed
gnomAD
CA397612803
rs1403028543
268 P>S No ClinGen
gnomAD
CA8277809
rs771764383
270 S>C No ClinGen
ExAC
gnomAD
rs1390347813
CA397612871
271 P>S No ClinGen
TOPMed
TCGA novel 272 P>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1452571528
CA397612947
275 G>R No ClinGen
TOPMed
gnomAD
rs1452571528
CA397612950
275 G>S No ClinGen
TOPMed
gnomAD
CA397613008
rs1555527879
279 Y>* No ClinGen
Ensembl
CA397613020
rs1296780097
280 K>R No ClinGen
gnomAD
CA397613045
rs1567556762
281 E>D No ClinGen
Ensembl
rs760530101
CA8277811
281 E>G No ClinGen
ExAC
gnomAD
CA397613075
rs1293151211
283 P>R No ClinGen
gnomAD
CA8277813
rs776960639
285 A>G No ClinGen
ExAC
TOPMed
gnomAD
CA8277812
rs769064912
285 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA397613117
rs1290656347
286 L>V No ClinGen
gnomAD
CA397613133
rs1459227384
287 P>A No ClinGen
TOPMed
rs1214681201
CA397613146
287 P>L No ClinGen
TOPMed
gnomAD
rs1214681201
CA397613147
287 P>Q No ClinGen
TOPMed
gnomAD
TCGA novel 291 P>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1597302421
CA397613216
292 L>M No ClinGen
Ensembl
rs750926221
CA8277817
293 P>S No ClinGen
ExAC
gnomAD
rs750926221
CA397613236
293 P>T No ClinGen
ExAC
gnomAD
rs1028740169
CA397613315
297 L>M No ClinGen
TOPMed
gnomAD
CA397613313
rs1028740169
297 L>V No ClinGen
TOPMed
gnomAD
CA397613332
rs1314754067
298 E>A No ClinGen
TOPMed
CA397613325
rs1237814549
298 E>K No ClinGen
TOPMed
CA286891431
rs957148101
299 E>A No ClinGen
TOPMed
gnomAD
rs989902013
CA286891437
299 E>D No ClinGen
TOPMed
gnomAD
rs1420620804
CA397613370
301 A>T No ClinGen
gnomAD
CA8277819
rs766746190
302 P>S No ClinGen
ExAC
gnomAD
CA286891442
rs766746190
302 P>T No ClinGen
ExAC
gnomAD
CA397613405
rs1357979527
303 P>L No ClinGen
TOPMed
gnomAD
CA397613400
rs1388326633
303 P>S No ClinGen
TOPMed
rs1284892106
CA397613436
305 D>G No ClinGen
gnomAD
TCGA novel 306 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA397613449
rs1372643859
306 P>S No ClinGen
gnomAD
CA397613475
rs978348590
308 R>H No ClinGen
TOPMed
gnomAD
CA286891448
rs978348590
308 R>L No ClinGen
TOPMed
gnomAD
rs1311657168
CA397613482
309 G>S No ClinGen
gnomAD
TCGA novel 310 G>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA397613544
rs1217138935
312 G>D No ClinGen
gnomAD
CA397613559
rs1425493284
313 S>G No ClinGen
gnomAD
rs1440665971
CA397613609
315 G>E No ClinGen
gnomAD
CA397613616
rs1267418781
316 P>S No ClinGen
TOPMed
CA397613615
rs1267418781
316 P>T No ClinGen
TOPMed
CA8277822
rs777445557
317 E>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1438479759
CA397613677
319 P>H No ClinGen
TOPMed
gnomAD
CA397613683
rs1438479759
319 P>R No ClinGen
TOPMed
gnomAD
CA8277823
rs753511807
319 P>S No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 320 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs756743681
CA8277824
320 G>S No ClinGen
ExAC
gnomAD
CA286891454
rs866721959
322 P>L No ClinGen
Ensembl
CA8277825
rs778416654
323 D>N No ClinGen
ExAC
gnomAD
CA397613785
rs1567556893
324 G>A No ClinGen
Ensembl
CA397613779
rs1423454091
324 G>R No ClinGen
TOPMed
gnomAD
rs780132156
CA8277828
327 L>V No ClinGen
ExAC
gnomAD
rs746838985
CA8277829
328 L>F No ClinGen
ExAC
gnomAD
rs768547596
CA8277830
330 R>C No ClinGen
ExAC
gnomAD
rs916748220
CA286891483
330 R>H No ClinGen
TOPMed
gnomAD
rs916748220
CA397613904
330 R>L No ClinGen
TOPMed
gnomAD
rs868456300
CA286891485
331 W>* No ClinGen
Ensembl
rs1380279666
CA397613911
331 W>R No ClinGen
TOPMed
rs866171316
CA286891493
334 H>Q No ClinGen
gnomAD
rs1391139410
CA397613986
334 H>R No ClinGen
TOPMed
rs1279156170
CA397613988
335 E>K No ClinGen
gnomAD
rs868502185
CA286891498
336 P>Q No ClinGen
Ensembl
CA286891496
rs867926437
336 P>T No ClinGen
Ensembl
CA397614025
rs930692347
337 G>R No ClinGen
TOPMed
gnomAD
CA286891499
rs930692347
337 G>S No ClinGen
TOPMed
gnomAD
CA286891500
rs865794936
337 G>V No ClinGen
Ensembl
CA286891502
rs886421097
338 L>R No ClinGen
TOPMed
rs373870177
CA8277831
338 L>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA286891507
rs867965018
340 S>I No ClinGen
Ensembl
CA286891509
rs867965018
340 S>N No ClinGen
Ensembl
CA286891513
rs868254796
342 G>C No ClinGen
Ensembl
CA286891515
rs867128800
342 G>D No ClinGen
Ensembl
CA397614161
rs1376300922
344 E>G No ClinGen
gnomAD
CA286891523
rs867938694
345 L>M No ClinGen
Ensembl
CA286891526
rs868112798
346 G>C No ClinGen
gnomAD
CA397614189
rs867271401
346 G>D No ClinGen
gnomAD
rs867271401
CA286891528
346 G>V No ClinGen
gnomAD
rs769768563
CA8277833
347 R>G No ClinGen
ExAC
gnomAD
rs773285181
CA8277834
347 R>L No ClinGen
ExAC
TOPMed
gnomAD
rs773285181
CA286891532
347 R>P No ClinGen
ExAC
TOPMed
gnomAD
CA397614195
rs773285181
347 R>Q No ClinGen
ExAC
TOPMed
gnomAD
CA397614200
rs1440473388
348 E>K No ClinGen
TOPMed
gnomAD
CA397614205
rs1440473388
348 E>Q No ClinGen
TOPMed
gnomAD
CA397614227
rs1438425349
349 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA397614219
rs1329139685
349 R>S No ClinGen
TOPMed
gnomAD
CA397614239
rs1317263419
350 G>C No ClinGen
TOPMed
gnomAD
rs752034419
CA8277837
350 G>D No ClinGen
ExAC
gnomAD
rs1317263419
CA397614242
350 G>R No ClinGen
TOPMed
gnomAD
rs1208878873
CA397614275
352 P>A No ClinGen
gnomAD
CA397614280
rs1264914860
352 P>H No ClinGen
gnomAD
CA397614278
rs1264914860
352 P>L No ClinGen
gnomAD
CA397614276
rs1208878873
352 P>S No ClinGen
gnomAD
CA397614289
rs1200080366
353 S>G No ClinGen
gnomAD
CA397614301
CA397614304
rs1262877509
353 S>R No ClinGen
TOPMed
gnomAD
CA8277841
rs767823724
354 E>K No ClinGen
ExAC
TOPMed
gnomAD
CA8277840
rs767823724
354 E>Q No ClinGen
ExAC
TOPMed
gnomAD
CA397614336
rs756871471
355 R>C No ClinGen
ExAC
TOPMed
gnomAD
CA8277842
rs756871471
355 R>G No ClinGen
ExAC
TOPMed
gnomAD
CA397614384
rs1482289898
357 E>D No ClinGen
gnomAD
rs764781885
CA8277843
357 E>G No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 358 E>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1597302699
CA397614421
359 R>H No ClinGen
Ensembl
rs1161529147
CA397614428
360 G>S No ClinGen
gnomAD
CA397614481
rs1336292140
363 A>T No ClinGen
TOPMed
CA397614502
rs1324003623
364 A>T No ClinGen
gnomAD
CA397614509
rs1415091611
365 V>I No ClinGen
TOPMed
CA8277844
rs750013547
367 P>L No ClinGen
ExAC
gnomAD
CA397614547
rs1396434462
367 P>S No ClinGen
TOPMed
rs757948661
CA8277846
368 G>E No ClinGen
ExAC
gnomAD
CA8277847
rs780187335
369 G>E No ClinGen
ExAC
gnomAD
rs780187335
CA397614589
369 G>V No ClinGen
ExAC
gnomAD
CA8277849
rs182733310
370 P>A No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA8277850
rs182733310
370 P>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA397614595
rs182733310
370 P>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1567557055
TCGA novel
371 P>R Variant assessed as Somatic; 0.0 impact. Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1176257409
CA397614646
373 G>D No ClinGen
gnomAD
CA397614642
rs1263139373
373 G>S No ClinGen
gnomAD
CA397614680
rs1285776132
375 A>E No ClinGen
gnomAD
CA397614682
rs1285776132
375 A>V No ClinGen
gnomAD
CA397614689
rs1487479330
376 P>A No ClinGen
gnomAD
TCGA novel 376 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1211679088
CA397614720
377 P>L No ClinGen
TOPMed
rs1401739471
CA397614713
377 P>S No ClinGen
gnomAD
rs770113556
CA8277852
378 P>A No ClinGen
ExAC
gnomAD
rs1449649413
CA397614737
378 P>L No ClinGen
gnomAD
CA286891578
rs772837738
379 R>G No ClinGen
TOPMed
gnomAD
CA286891581
rs981547690
379 R>H No ClinGen
TOPMed
rs1473262157
CA397614766
380 Y>F No ClinGen
TOPMed
gnomAD
CA286891584
rs1035274741
381 P>A No ClinGen
TOPMed
rs1158215470
CA397614784
382 G>C No ClinGen
gnomAD
rs1372984057
CA397614821
384 L>V No ClinGen
gnomAD
rs1275174545
CA397614842
385 D>E No ClinGen
TOPMed
CA397614846
rs1244940503
386 G>R No ClinGen
TOPMed
CA397614848
rs1244940503
386 G>W No ClinGen
TOPMed
rs1417707626
CA397614885
388 G>A No ClinGen
gnomAD
rs770978873
CA8277855
389 A>E No ClinGen
ExAC
gnomAD
CA8277854
rs749428578
389 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs1310631133
CA397614953
392 D>G No ClinGen
gnomAD
rs866308900
CA286891601
393 G>S No ClinGen
Ensembl
rs373366887
CA286891603
394 D>N No ClinGen
Ensembl
TCGA novel 395 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1307992765
CA397615046
396 Y>C No ClinGen
gnomAD
rs1351046226
CA397615084
398 S>I No ClinGen
TOPMed
gnomAD
CA397615089
rs1351046226
398 S>T No ClinGen
TOPMed
gnomAD
CA397615107
rs1472850001
399 S>N No ClinGen
TOPMed
rs1287162089
CA397615124
400 S>N No ClinGen
gnomAD
rs370995439
CA397615132
400 S>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA397615164
rs1484019584
402 E>G No ClinGen
TOPMed
TCGA novel 402 E>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA286891609
rs1001281747
403 T>N No ClinGen
Ensembl
CA397615207
rs1258368633
404 G>D No ClinGen
gnomAD
CA397615249
rs1178099328
406 S>R No ClinGen
gnomAD
CA286891620
rs930834471
409 P>A No ClinGen
TOPMed
gnomAD
CA286891622
rs984823575
410 S>R No ClinGen
TOPMed
rs1465501295
CA397615332
411 P>Q No ClinGen
gnomAD
CA8277864
rs750020757
411 P>T No ClinGen
ExAC
TOPMed
gnomAD
CA8277867
rs765947575
412 P>L No ClinGen
ExAC
gnomAD
rs765947575
CA8277866
412 P>R No ClinGen
ExAC
gnomAD
CA8277868
rs754906814
413 G>C No ClinGen
ExAC
gnomAD
rs1330073462
CA397615363
413 G>D No ClinGen
gnomAD
rs748045093
CA8277870
414 G>D No ClinGen
ExAC
rs749466686
CA8277873
417 E>G No ClinGen
ExAC
TOPMed
gnomAD
rs778109842
CA8277872
417 E>K No ClinGen
ExAC
gnomAD
rs1258360260
CA397615427
418 G>D No ClinGen
TOPMed
gnomAD
rs1258360260
CA397615431
418 G>V No ClinGen
TOPMed
gnomAD
rs1236402719
CA397615448
419 Y>C No ClinGen
gnomAD
CA286891649
rs745930978
419 Y>H No ClinGen
ExAC
gnomAD
CA8277876
rs745930978
419 Y>N No ClinGen
ExAC
gnomAD
rs576649513
CA8277878
420 P>A No ClinGen
1000Genomes
ExAC
gnomAD
rs576649513
CA8277877
420 P>T No ClinGen
1000Genomes
ExAC
gnomAD
rs764316328
CA8277880
423 H>Q No ClinGen
ExAC
TOPMed
gnomAD
rs761148812
CA8277879
423 H>R No ClinGen
ExAC
TOPMed
gnomAD
CA8277882
rs762627354
424 L>P No ClinGen
ExAC
gnomAD
CA8277881
rs772948679
424 L>V No ClinGen
ExAC
TOPMed
gnomAD
CA397615540
rs1470233457
425 A>D No ClinGen
TOPMed
gnomAD
CA397615533
rs1379359210
425 A>T No ClinGen
gnomAD
CA397615544
rs1470233457
425 A>V No ClinGen
TOPMed
gnomAD
CA397615555
rs1397441456
426 Y>C No ClinGen
gnomAD
CA397615595
rs1198511855
428 E>D No ClinGen
TOPMed
CA8277885
rs759114108
429 P>R No ClinGen
ExAC
gnomAD
rs1298328046
CA397615603
429 P>S No ClinGen
gnomAD
TCGA novel 431 S>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8277890
rs754069212
431 S>R No ClinGen
ExAC
gnomAD
TCGA novel 437 Y>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8277893
rs745984814
437 Y>C No ClinGen
ExAC
gnomAD
COSM1381413
rs1016949003
CA286891692
438 V>M large_intestine Variant assessed as Somatic; impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
Ensembl
NCI-TCGA
CA397615881
rs1192780961
443 G>D No ClinGen
gnomAD
CA8277897
rs769067993
443 G>S No ClinGen
ExAC
TOPMed
gnomAD
CA397615937
rs1348998750
447 P>S No ClinGen
gnomAD
rs1295688575
CA397615950
448 S>G No ClinGen
gnomAD
CA397615955
rs1346487914
448 S>N No ClinGen
gnomAD
CA397616022
rs1276779955
451 Q>R No ClinGen
gnomAD
CA397616055
rs1467658215
453 N>H No ClinGen
gnomAD
CA397616073
rs1215299206
453 N>K No ClinGen
gnomAD
rs1312064521
CA397616092
454 A>V No ClinGen
gnomAD
rs765775523
CA286891705
456 V>M Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
CA8277901
rs774117085
457 E>Q No ClinGen
ExAC
gnomAD
CA397616182
rs1267007535
460 V>M No ClinGen
gnomAD
rs759137418
CA286891712
461 E>A No ClinGen
ExAC
TOPMed
gnomAD
CA397616200
rs759137418
461 E>G No ClinGen
ExAC
TOPMed
gnomAD
rs759137418
CA8277902
461 E>V No ClinGen
ExAC
TOPMed
gnomAD
rs371242587
CA8277903
463 E>D No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1478751277
CA397616215
463 E>K No ClinGen
gnomAD
rs1412399586
CA397616228
464 E>K No ClinGen
gnomAD
CA8277904
rs752714744
465 A>P No ClinGen
ExAC
gnomAD
CA397616250
rs987306609
466 L>V No ClinGen
TOPMed
gnomAD
rs202115526
CA8277906
468 G>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs202115526
CA8277907
468 G>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA8277909
rs544540526
469 R>K No ClinGen
ExAC
TOPMed
gnomAD
CA8277908
rs544540526
469 R>T No ClinGen
ExAC
TOPMed
gnomAD
CA8277910
rs750592784
470 A>T No ClinGen
ExAC
gnomAD
CA397616316
rs1175068964
472 A>V No ClinGen
TOPMed
rs779930290
CA8277912
473 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs1316079632
CA397616327
473 A>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA8277914
rs769101192
475 V>M No ClinGen
ExAC
TOPMed
gnomAD
rs201599490
RCV000970021
CA8277915
476 A>T No ClinGen
ClinVar
1000Genomes
ExAC
TOPMed
dbSNP
gnomAD
rs748565761
CA8277916
477 A>S No ClinGen
ExAC
gnomAD
rs748565761
CA397616363
477 A>T No ClinGen
ExAC
gnomAD
CA397616372
rs1481948501
477 A>V No ClinGen
gnomAD
rs1055539545
CA286891746
478 G>A No ClinGen
Ensembl
rs774172155
CA8277918
479 A>T No ClinGen
ExAC
gnomAD
rs1157269159
CA397616397
480 A>S No ClinGen
gnomAD
CA8277919
rs759074454
480 A>V No ClinGen
ExAC
gnomAD
rs1262663182
CA397616404
481 G>S No ClinGen
TOPMed
rs371934522
CA397616419
482 L>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs371934522
CA8277921
482 L>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1214385812
CA397616434
484 P>H No ClinGen
TOPMed
rs760223111
CA8277922
484 P>T No ClinGen
ExAC
TOPMed
gnomAD
CA397616441
rs1222111385
485 P>L No ClinGen
TOPMed
gnomAD
rs776525632
CA8277924
485 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs1376494484
CA397616443
486 F>V No ClinGen
gnomAD
rs376477815
CA8277927
489 G>D No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA8277926
rs764969310
489 G>S No ClinGen
ExAC
gnomAD
CA8277928
CA8277929
rs370020453
490 G>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs751657140
CA8277930
491 D>A No ClinGen
ExAC
TOPMed
gnomAD
rs1243183975
CA397616483
492 K>N No ClinGen
gnomAD
rs964070713
CA286891805
494 A>P No ClinGen
gnomAD
CA397616491
rs964070713
494 A>T No ClinGen
gnomAD
CA397616495
rs1388154326
494 A>V No ClinGen
TOPMed
rs748619078
CA8277933
495 G>E No ClinGen
ExAC
gnomAD
rs1242738283
CA397616497
495 G>R No ClinGen
TOPMed
rs756581340
CA8277934
496 A>S No ClinGen
ExAC
TOPMed
gnomAD
rs778220665
CA8277935
498 G>C No ClinGen
ExAC
TOPMed
gnomAD
rs778220665
CA8277936
498 G>S No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 498 G>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA397616519
rs1597303436
499 G>D No ClinGen
Ensembl
rs775173256
CA8277938
501 G>E No ClinGen
ExAC
TOPMed
gnomAD
rs771684583
CA8277937
501 G>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs1444864162
CA397616553
505 R>L No ClinGen
gnomAD
TCGA novel 505 R>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1336569288
CA397616556
506 P>S No ClinGen
gnomAD
CA397616586
rs1340637403
510 A>G No ClinGen
TOPMed
COSM1609937
COSM3717224
rs1225222665
CA397616582
510 A>T liver [Cosmic] No ClinGen
cosmic curated
gnomAD
rs765029246
CA8277943
511 S>L No ClinGen
ExAC
gnomAD
CA8277944
rs772938021
513 D>N No ClinGen
ExAC
gnomAD
CA397616620
rs1245308453
515 S>T No ClinGen
gnomAD
rs1365533672
CA397616625
516 Y>H No ClinGen
TOPMed
rs1423019119
CA397616653
519 P>L No ClinGen
gnomAD
CA397616650
rs1555528024
519 P>S No ClinGen
Ensembl
CA397616665
rs1464192791
521 T>M No ClinGen
gnomAD
CA397616680
rs1404953395
524 Q>R No ClinGen
gnomAD
rs766550622
CA397616693
526 E>* No ClinGen
ExAC
TOPMed
gnomAD
CA397616692
rs766550622
526 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs766550622
CA8277946
526 E>Q No ClinGen
ExAC
TOPMed
gnomAD
rs751785211
CA8277947
528 T>M No ClinGen
ExAC
gnomAD
CA397616730
rs767666852
531 L>V No ClinGen
ExAC
TOPMed
gnomAD
rs1398267371
CA397616738
532 T>S No ClinGen
TOPMed
gnomAD
CA397616747
rs1271400152
534 P>S No ClinGen
gnomAD
rs1206340086
CA397616761
536 P>A No ClinGen
TOPMed
rs749649991
CA397616786
539 I>M No ClinGen
ExAC
TOPMed
gnomAD
CA397616780
rs1288189144
539 I>V No ClinGen
gnomAD
rs1567557779
CA397616809
541 G>E No ClinGen
Ensembl
TCGA novel 544 F>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1195466317
CA397616874
545 T>M No ClinGen
gnomAD
TCGA novel 549 T>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA397617031
rs1363491742
555 R>C No ClinGen
gnomAD
rs868613726
CA286891871
558 L>P No ClinGen
Ensembl
TCGA novel 559 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA286891880
rs767958003
564 A>E No ClinGen
Ensembl
rs1319745856
CA397617136
566 D>N No ClinGen
gnomAD
CA397617160
rs1282140691
569 G>S No ClinGen
gnomAD
TCGA novel 583 R>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA286891891
rs1055868817
586 S>* No ClinGen
TOPMed
CA397617281
rs1055868817
586 S>L No ClinGen
TOPMed
CA8277966
rs767724011
588 E>K No ClinGen
ExAC
gnomAD
CA8277968
rs760801895
592 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs764571799
CA8277969
594 Q>H No ClinGen
ExAC
gnomAD
CA397617336
rs1385579986
594 Q>P No ClinGen
gnomAD
CA397617340
rs1331592768
595 V>M No ClinGen
gnomAD
CA397617356
rs1325649512
597 G>D No ClinGen
Ensembl
rs754317127
CA8277970
597 G>R No ClinGen
ExAC
gnomAD
rs1244832850
CA397617359
598 G>S Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA397617371
rs1241812192
599 K>N No ClinGen
gnomAD
CA8277976
rs533264563
608 S>N No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs769279920
CA8277977
610 M>R No ClinGen
ExAC
gnomAD
rs949815126
CA286891930
615 V>M No ClinGen
Ensembl
rs774144113
CA8277981
616 G>R No ClinGen
ExAC
TOPMed
gnomAD
CA397617497
rs1465453896
617 G>D No ClinGen
gnomAD
rs772459357
CA8277984
618 A>P No ClinGen
ExAC
gnomAD
rs199947545
CA8277985
620 G>S No ClinGen
1000Genomes
ExAC
gnomAD
rs760854984
CA8277987
621 A>E No ClinGen
ExAC
gnomAD
CA397617516
rs1393550030
621 A>T No ClinGen
gnomAD
CA286891943
rs986169306
622 A>V No ClinGen
TOPMed
rs570067922
CA286891946
623 G>R No ClinGen
1000Genomes
TOPMed
CA397617535
rs1231649875
624 A>V No ClinGen
gnomAD
rs1324289726
CA397617544
626 A>E No ClinGen
gnomAD
CA8277988
rs764170963
626 A>P No ClinGen
ExAC
gnomAD
CA397617550
rs1198088743
627 G>D No ClinGen
gnomAD
rs1390853458
CA397617564
629 G>A No ClinGen
TOPMed
CA397617560
rs1481725451
CA397617561
629 G>R No ClinGen
gnomAD
CA8277989
rs754336125
630 G>E No ClinGen
ExAC
TOPMed
gnomAD
rs1250918654
CA397617579
632 P>S No ClinGen
gnomAD
rs887258154
CA286891956
633 G>S No ClinGen
gnomAD
rs1383799421
CA397617592
634 V>A No ClinGen
gnomAD
CA397617593
rs1383799421
634 V>G No ClinGen
gnomAD
rs765640737
CA8277991
637 P>H No ClinGen
ExAC
TOPMed
gnomAD
CA286891965
rs924415108
637 P>S No ClinGen
TOPMed
rs1159592474
CA397617611
638 D>N No ClinGen
gnomAD
CA397617610
rs1159592474
638 D>Y No ClinGen
gnomAD
CA8277993
rs758757068
639 G>S No ClinGen
ExAC
gnomAD
CA397617638
rs1346686743
642 K>E No ClinGen
gnomAD
rs1309513784
CA397617651
644 D>N No ClinGen
TOPMed
gnomAD
TCGA novel 646 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs188260013
CA8277997
646 P>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs749203118
CA8277998
647 E>Q No ClinGen
ExAC
gnomAD
rs770947270
CA286891986
649 V>F No ClinGen
ExAC
TOPMed
gnomAD
CA8277999
rs770947270
649 V>L No ClinGen
ExAC
TOPMed
gnomAD
rs200496232
CA397619112
654 R>L No ClinGen
TOPMed
gnomAD
CA286891989
rs200496232
654 R>P No ClinGen
TOPMed
gnomAD
CA397619123
rs1170628410
655 L>P No ClinGen
gnomAD
rs530936134
CA8278000
655 L>V No ClinGen
ExAC
TOPMed
gnomAD
CA8278002
rs771939213
657 A>T No ClinGen
ExAC
gnomAD
CA8278006
rs776821926
661 S>N No ClinGen
ExAC
TOPMed
gnomAD
CA397619225
rs1215388577
661 S>R No ClinGen
gnomAD
CA8278007
rs555845769
662 L>M No ClinGen
1000Genomes
ExAC
gnomAD
CA397619227
rs555845769
662 L>V No ClinGen
1000Genomes
ExAC
gnomAD
CA397619264
CA397619266
rs1243562233
664 Q>H No ClinGen
TOPMed
gnomAD
CA8278008
rs765840182
665 Q>H No ClinGen
ExAC
gnomAD
rs1293622520
CA397619274
665 Q>R No ClinGen
gnomAD
CA8278009
rs373603534
666 D>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1486598627
CA397619307
667 K>N No ClinGen
TOPMed
gnomAD
rs1186577844
CA397619311
668 A>T No ClinGen
TOPMed
gnomAD
rs1225873659
CA397619323
670 A>E No ClinGen
TOPMed
CA8278011
rs766662445
670 A>T No ClinGen
ExAC
gnomAD
TCGA novel 671 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8278013
rs755740828
672 E>Q No ClinGen
ExAC
gnomAD
CA8278014
rs763628789
675 A>E No ClinGen
ExAC
TOPMed
gnomAD
CA397619355
rs1347461145
675 A>T No ClinGen
gnomAD
rs1454737849
CA397619386
677 T>A No ClinGen
gnomAD
CA397619419
rs1316908986
679 H>Q No ClinGen
gnomAD
rs756712980
CA8278016
680 F>C No ClinGen
ExAC
gnomAD
CA286892036
rs925851450
683 D>N No ClinGen
Ensembl
rs1261928101
CA397619491
684 P>R No ClinGen
gnomAD
rs779011742
CA8278017
684 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs1318627856 685 K>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No NCI-TCGA
rs991141113
CA286892042
687 A>T No ClinGen
TOPMed
gnomAD
CA397619534
rs1167160414
687 A>V No ClinGen
TOPMed
CA8278018
rs745736256
690 S>N No ClinGen
ExAC
gnomAD
CA8278020
rs779947741
692 Y>C No ClinGen
ExAC
gnomAD
TCGA novel 693 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA397619622
rs1175479430
693 P>Q No ClinGen
gnomAD
CA397619638
rs1471080020
695 A>T No ClinGen
gnomAD
rs1221649265
CA397619670
697 F>V No ClinGen
gnomAD
CA8278022
rs768965384
698 T>M No ClinGen
ExAC
gnomAD
rs1277522320
CA397619701
699 A>D No ClinGen
gnomAD
CA397619695
rs1391666684
699 A>T No ClinGen
TOPMed
rs1224227061
CA397619737
702 G>D Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs1320719666
CA397619756
704 S>G No ClinGen
gnomAD
CA8278025
rs769704666
704 S>N No ClinGen
ExAC
CA8278026
rs535246535
705 P>A No ClinGen
1000Genomes
ExAC
gnomAD
CA397619772
rs1263439729
705 P>H No ClinGen
gnomAD
CA397619769
rs535246535
705 P>T No ClinGen
1000Genomes
ExAC
gnomAD
CA8278027
CA397619785
rs763409414
706 D>E No ClinGen
ExAC
TOPMed
gnomAD
rs997728333
CA286892068
706 D>N No ClinGen
TOPMed
CA8278028
rs766750503
708 A>E No ClinGen
ExAC
TOPMed
gnomAD
rs1234909584
CA397619794
708 A>T No ClinGen
gnomAD
rs577957580
CA8278030
710 E>D No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA286892077
rs1046791154
710 E>K No ClinGen
Ensembl
rs1177211839
CA397619817
711 V>E No ClinGen
gnomAD
rs1481491486
CA397619814
711 V>L No ClinGen
TOPMed
gnomAD
rs1481491486
CA397619812
711 V>M No ClinGen
TOPMed
gnomAD
rs543718567
CA8278031
712 L>M No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1408382961
CA397619822
713 S>R No ClinGen
TOPMed
gnomAD
rs1286064763
CA397619826
713 S>T No ClinGen
TOPMed
CA397619840
rs1356005479
714 Q>H No ClinGen
gnomAD
rs1282640036
CA397619849
715 G>D No ClinGen
gnomAD
CA8278033
rs756799893
715 G>S No ClinGen
ExAC
gnomAD
CA397619896
rs1426001071
719 A>E No ClinGen
TOPMed
gnomAD
CA397619894
rs1426001071
719 A>V No ClinGen
TOPMed
gnomAD
CA8278035
CA286892095
rs750411726
721 G>R No ClinGen
ExAC
TOPMed
gnomAD
rs1212376961
CA397619943
724 G>D No ClinGen
gnomAD
rs1063317
CA286892100
VAR_063109
725 R>G No ClinGen
UniProt
Ensembl
dbSNP
CA286892101
rs968722937
726 T>A No ClinGen
TOPMed
CA8278036
rs758461921
726 T>I No ClinGen
ExAC
TOPMed
CA397619984
rs1275557231
728 D>V No ClinGen
gnomAD
rs1164517290
CA397619993
729 R>G No ClinGen
TOPMed
rs1438822118
CA397619995
729 R>H No ClinGen
gnomAD
CA286892107
rs924582239
730 F>L No ClinGen
TOPMed
gnomAD
rs1411150266
CA397620011
730 F>L No ClinGen
TOPMed
rs780109649
CA8278037
732 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA8278038
rs746888597
733 T>I No ClinGen
ExAC
TOPMed
gnomAD
rs746888597
CA286892112
733 T>S No ClinGen
ExAC
TOPMed
gnomAD

No associated diseases with Q14526

6 regional properties for Q14526

Type Name Position InterPro Accession
domain BTB/POZ domain 37 - 153 IPR000210
domain Zinc finger C2H2-type 437 - 464 IPR013087-1
domain Zinc finger C2H2-type 507 - 534 IPR013087-2
domain Zinc finger C2H2-type 535 - 562 IPR013087-3
domain Zinc finger C2H2-type 563 - 590 IPR013087-4
domain Zinc finger C2H2-type 591 - 614 IPR013087-5

Functions

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

3 GO annotations of cellular component

Name Definition
chromatin The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome.
nucleoplasm That part of the nuclear content other than the chromosomes or the nucleolus.
nucleus A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent.

8 GO annotations of molecular function

Name Definition
DNA-binding transcription factor activity A transcription regulator activity that modulates transcription of gene sets via selective and non-covalent binding to a specific double-stranded genomic DNA sequence (sometimes referred to as a motif) within a cis-regulatory region. Regulatory regions include promoters (proximal and distal) and enhancers. Genes are transcriptional units, and include bacterial operons.
DNA-binding transcription factor activity, RNA polymerase II-specific A DNA-binding transcription factor activity that modulates the transcription of specific gene sets transcribed by RNA polymerase II.
DNA-binding transcription repressor activity, RNA polymerase II-specific A DNA-binding transcription factor activity that represses or decreases the transcription of specific gene sets transcribed by RNA polymerase II.
histone deacetylase binding Binding to histone deacetylase.
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 DNA binding Binding to DNA of a specific nucleotide composition, e.g. GC-rich DNA binding, or with a specific sequence motif or type of DNA e.g. promotor binding or rDNA binding.
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.

7 GO annotations of biological process

Name Definition
intrinsic apoptotic signaling pathway in response to DNA damage The series of molecular signals in which an intracellular signal is conveyed to trigger the apoptotic death of a cell. The pathway is induced by the detection of DNA damage, and ends when the execution phase of apoptosis is triggered.
negative regulation of transcription by RNA polymerase II Any process that stops, prevents, or reduces the frequency, rate or extent of transcription mediated by RNA polymerase II.
negative regulation of Wnt signaling pathway Any process that stops, prevents, or reduces the frequency, rate or extent of the Wnt signaling pathway.
positive regulation of DNA damage response, signal transduction by p53 class mediator Any process that activates, maintains or increases the rate of the cascade of processes induced by the cell cycle regulator phosphoprotein p53, or an equivalent protein, in response to the detection of DNA damage.
regulation of DNA-templated transcription Any process that modulates the frequency, rate or extent of cellular DNA-templated transcription.
regulation of transcription by RNA polymerase II Any process that modulates the frequency, rate or extent of transcription mediated by RNA polymerase II.
Wnt signaling pathway The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell and ending with a change in cell state.

178 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q08DS3 OSR1 Protein odd-skipped-related 1 Bos taurus (Bovine) PR
Q2VWH6 FEZF2 Fez family zinc finger protein 2 Bos taurus (Bovine) PR
A6QNZ0 ZSCAN26 Zinc finger and SCAN domain-containing protein 26 Bos taurus (Bovine) PR
A7MBI1 ZFP69 Zinc finger protein 69 homolog Bos taurus (Bovine) PR
Q08705 CTCF Transcriptional repressor CTCF Gallus gallus (Chicken) PR
O42409 GFI1B Zinc finger protein Gfi-1b Gallus gallus (Chicken) PR
A2T6W2 ZNF449 Zinc finger protein 449 Pan troglodytes (Chimpanzee) PR
Q9U405 grau Transcription factor grauzone Drosophila melanogaster (Fruit fly) PR
Q7K0S9 sug Zinc finger protein GLIS2 homolog Drosophila melanogaster (Fruit fly) PR
P20385 Cf2 Chorion transcription factor Cf2 Drosophila melanogaster (Fruit fly) PR
Q86P48 ATbp AT-rich binding protein Drosophila melanogaster (Fruit fly) PR
P28698 MZF1 Myeloid zinc finger 1 Homo sapiens (Human) PR
Q9NTW7 ZFP64 Zinc finger protein 64 Homo sapiens (Human) PR
O14978 ZNF263 Zinc finger protein 263 Homo sapiens (Human) PR
O60304 ZNF500 Zinc finger protein 500 Homo sapiens (Human) PR
P08151 GLI1 Zinc finger protein GLI1 Homo sapiens (Human) PR
P18146 EGR1 Early growth response protein 1 Homo sapiens (Human) PR
Q9Y5W3 KLF2 Krueppel-like factor 2 Homo sapiens (Human) PR
Q9UNY5 ZNF232 Zinc finger protein 232 Homo sapiens (Human) PR
Q96SZ4 ZSCAN10 Zinc finger and SCAN domain-containing protein 10 Homo sapiens (Human) PR
P17028 ZNF24 Zinc finger protein 24 Homo sapiens (Human) PR
P57682 KLF3 Krueppel-like factor 3 Homo sapiens (Human) PR
P25490 YY1 Transcriptional repressor protein YY1 Homo sapiens (Human) SS
O43296 ZNF264 Zinc finger protein 264 Homo sapiens (Human) PR
P49711 CTCF Transcriptional repressor CTCF Homo sapiens (Human) PR
Q9NQX1 PRDM5 PR domain zinc finger protein 5 Homo sapiens (Human) PR
Q9HBE1 PATZ1 POZ-, AT hook-, and zinc finger-containing protein 1 Homo sapiens (Human) PR
Q8TAX0 OSR1 Protein odd-skipped-related 1 Homo sapiens (Human) PR
Q9UL58 ZNF215 Zinc finger protein 215 Homo sapiens (Human) PR
Q8TBJ5 FEZF2 Fez family zinc finger protein 2 Homo sapiens (Human) PR
Q96SR6 ZNF382 Zinc finger protein 382 Homo sapiens (Human) PR
Q96IT1 ZNF496 Zinc finger protein 496 Homo sapiens (Human) PR
Q96N95 ZNF396 Zinc finger protein 396 Homo sapiens (Human) PR
O75840 KLF7 Krueppel-like factor 7 Homo sapiens (Human) PR
Q9H9D4 ZNF408 Zinc finger protein 408 Homo sapiens (Human) PR
Q13127 REST RE1-silencing transcription factor Homo sapiens (Human) PR
Q8IZM8 ZNF654 Zinc finger protein 654 Homo sapiens (Human) PR
P17022 ZNF18 Zinc finger protein 18 Homo sapiens (Human) PR
Q86XF7 ZNF575 Zinc finger protein 575 Homo sapiens (Human) PR
Q06889 EGR3 Early growth response protein 3 Homo sapiens (Human) PR
Q8NAM6 ZSCAN4 Zinc finger and SCAN domain-containing protein 4 Homo sapiens (Human) PR
Q08ER8 ZNF543 Zinc finger protein 543 Homo sapiens (Human) PR
P17029 ZKSCAN1 Zinc finger protein with KRAB and SCAN domains 1 Homo sapiens (Human) PR
Q8N680 ZBTB2 Zinc finger and BTB domain-containing protein 2 Homo sapiens (Human) PR
O95625 ZBTB11 Zinc finger and BTB domain-containing protein 11 Homo sapiens (Human) PR
Q9NPC7 MYNN Myoneurin Homo sapiens (Human) PR
Q96BV0 ZNF775 Zinc finger protein 775 Homo sapiens (Human) PR
Q8NF99 ZNF397 Zinc finger protein 397 Homo sapiens (Human) PR
Q63HK3 ZKSCAN2 Zinc finger protein with KRAB and SCAN domains 2 Homo sapiens (Human) PR
Q5FWF6 ZNF789 Zinc finger protein 789 Homo sapiens (Human) PR
Q15776 ZKSCAN8 Zinc finger protein with KRAB and SCAN domains 8 Homo sapiens (Human) PR
Q53GI3 ZNF394 Zinc finger protein 394 Homo sapiens (Human) PR
O95125 ZNF202 Zinc finger protein 202 Homo sapiens (Human) PR
Q05516 ZBTB16 Zinc finger and BTB domain-containing protein 16 Homo sapiens (Human) PR
Q9H116 GZF1 GDNF-inducible zinc finger protein 1 Homo sapiens (Human) PR
Q8N0Y2 ZNF444 Zinc finger protein 444 Homo sapiens (Human) PR
Q6P9G9 ZNF449 Zinc finger protein 449 Homo sapiens (Human) PR
Q8IW36 ZNF695 Zinc finger protein 695 Homo sapiens (Human) PR
Q5VTD9 GFI1B Zinc finger protein Gfi-1b Homo sapiens (Human) PR
Q6PG37 ZNF790 Zinc finger protein 790 Homo sapiens (Human) PR
Q9NQV6 PRDM10 PR domain zinc finger protein 10 Homo sapiens (Human) PR
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
Q9BRR0 ZKSCAN3 Zinc finger protein with KRAB and SCAN domains 3 Homo sapiens (Human) PR
Q969J2 ZKSCAN4 Zinc finger protein with KRAB and SCAN domains 4 Homo sapiens (Human) PR
P49910 ZNF165 Zinc finger protein 165 Homo sapiens (Human) PR
Q9Y4X4 KLF12 Krueppel-like factor 12 Homo sapiens (Human) PR
P10074 ZBTB48 Telomere zinc finger-associated protein Homo sapiens (Human) PR
P17010 ZFX Zinc finger X-chromosomal protein Homo sapiens (Human) PR
Q9H5H4 ZNF768 Zinc finger protein 768 Homo sapiens (Human) PR
Q6NSZ9 ZSCAN25 Zinc finger and SCAN domain-containing protein 25 Homo sapiens (Human) PR
Q9Y2L8 ZKSCAN5 Zinc finger protein with KRAB and SCAN domains 5 Homo sapiens (Human) PR
Q86UZ6 ZBTB46 Zinc finger and BTB domain-containing protein 46 Homo sapiens (Human) PR
Q9NX65 ZSCAN32 Zinc finger and SCAN domain-containing protein 32 Homo sapiens (Human) PR
O14771 ZNF213 Zinc finger protein 213 Homo sapiens (Human) PR
Q8IWY8 ZSCAN29 Zinc finger and SCAN domain-containing protein 29 Homo sapiens (Human) PR
Q8NCP5 ZBTB44 Zinc finger and BTB domain-containing protein 44 Homo sapiens (Human) PR
P41182 BCL6 B-cell lymphoma 6 protein Homo sapiens (Human) PR
Q9NQX0 PRDM6 Putative histone-lysine N-methyltransferase PRDM6 Homo sapiens (Human) PR
Q9BU19 ZNF692 Zinc finger protein 692 Homo sapiens (Human) PR
Q08AG5 ZNF844 Zinc finger protein 844 Homo sapiens (Human) PR
Q6R2W3 ZBED9 SCAN domain-containing protein 3 Homo sapiens (Human) PR
P98182 ZNF200 Zinc finger protein 200 Homo sapiens (Human) PR
Q9UK11 ZNF223 Zinc finger protein 223 Homo sapiens (Human) PR
O15156 ZBTB7B Zinc finger and BTB domain-containing protein 7B Homo sapiens (Human) PR
Q6ZMS7 ZNF783 Zinc finger protein 783 Homo sapiens (Human) PR
P59923 ZNF445 Zinc finger protein 445 Homo sapiens (Human) PR
Q8N859 ZNF713 Zinc finger protein 713 Homo sapiens (Human) PR
Q99612 KLF6 Krueppel-like factor 6 Homo sapiens (Human) PR
Q8TD17 ZNF398 Zinc finger protein 398 Homo sapiens (Human) PR
P52739 ZNF131 Zinc finger protein 131 Homo sapiens (Human) PR
A6NGD5 ZSCAN5C Zinc finger and SCAN domain-containing protein 5C Homo sapiens (Human) PR
Q05215 EGR4 Early growth response protein 4 Homo sapiens (Human) PR
Q7Z398 ZNF550 Zinc finger protein 550 Homo sapiens (Human) PR
Q9Y2K1 ZBTB1 Zinc finger and BTB domain-containing protein 1 Homo sapiens (Human) PR
Q96N20 ZNF75A Zinc finger protein 75A Homo sapiens (Human) PR
A6NJL1 ZSCAN5B Zinc finger and SCAN domain-containing protein 5B Homo sapiens (Human) PR
A1YPR0 ZBTB7C Zinc finger and BTB domain-containing protein 7C Homo sapiens (Human) PR
Q9NWS9 ZNF446 Zinc finger protein 446 Homo sapiens (Human) PR
P24278 ZBTB25 Zinc finger and BTB domain-containing protein 25 Homo sapiens (Human) PR
Q96N38 ZNF714 Zinc finger protein 714 Homo sapiens (Human) PR
Q86YH2 ZNF280B Zinc finger protein 280B Homo sapiens (Human) PR
Q9UFB7 ZBTB47 Zinc finger and BTB domain-containing protein 47 Homo sapiens (Human) PR
Q9ULJ3 ZBTB21 Zinc finger and BTB domain-containing protein 21 Homo sapiens (Human) PR
Q9Y2D9 ZNF652 Zinc finger protein 652 Homo sapiens (Human) PR
O08584 Klf6 Krueppel-like factor 6 Mus musculus (Mouse) PR
Q61164 Ctcf Transcriptional repressor CTCF Mus musculus (Mouse) PR
Q810A1 Znf18 Zinc finger protein 18 Mus musculus (Mouse) PR
Q8BGS3 Zkscan1 Zinc finger protein with KRAB and SCAN domains 1 Mus musculus (Mouse) PR
Q00899 Yy1 Transcriptional repressor protein YY1 Mus musculus (Mouse) PR
P41183 Bcl6 B-cell lymphoma 6 protein homolog Mus musculus (Mouse) PR
Q9DAI4 Zbtb43 Zinc finger and BTB domain-containing protein 43 Mus musculus (Mouse) PR
O70237 Gfi1b Zinc finger protein Gfi-1b Mus musculus (Mouse) PR
Q99KZ6 Znf639 Zinc finger protein 639 Mus musculus (Mouse) PR
Q9Z1D9 Znf394 Zinc finger protein 394 Mus musculus (Mouse) PR
Q9CXE0 Prdm5 PR domain zinc finger protein 5 Mus musculus (Mouse) PR
P43300 Egr3 Early growth response protein 3 Mus musculus (Mouse) PR
Q9DAU9 Znf654 Zinc finger protein 654 Mus musculus (Mouse) PR
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
Q9R1Y5 Hic1 Hypermethylated in cancer 1 protein Mus musculus (Mouse) PR
Q9Z2K3 Znf394 Zinc finger protein 394 Rattus norvegicus (Rat) PR
Q642B9 Znf18 Zinc finger protein 18 Rattus norvegicus (Rat) PR
B0K011 Osr1 Protein odd-skipped-related 1 Rattus norvegicus (Rat) PR
D3ZUU2 Gzf1 GDNF-inducible zinc finger protein 1 Rattus norvegicus (Rat) PR
B1WBU4 Zbtb8a Zinc finger and BTB domain-containing protein 8A Rattus norvegicus (Rat) PR
Q7TNK3 Znf24 Zinc finger protein 24 Rattus norvegicus (Rat) PR
O35819 Klf6 Krueppel-like factor 6 Rattus norvegicus (Rat) PR
Q9R1D1 Ctcf Transcriptional repressor CTCF Rattus norvegicus (Rat) PR
P43301 Egr3 Early growth response protein 3 Rattus norvegicus (Rat) PR
P08154 Egr1 Early growth response protein 1 Rattus norvegicus (Rat) PR
A0JPL0 Znf382 Zinc finger protein 382 Rattus norvegicus (Rat) PR
Q4KLI1 Zkscan1 Zinc finger protein with KRAB and SCAN domains 1 Rattus norvegicus (Rat) PR
A1L1J6 Znf652 Zinc finger protein 652 Rattus norvegicus (Rat) PR
Q9SHD0 ZAT4 Zinc finger protein ZAT4 Arabidopsis thaliana (Mouse-ear cress) PR
Q9LFU0 DOT3 BTB/POZ domain-containing protein DOT3 Arabidopsis thaliana (Mouse-ear cress) PR
Q0P4X6 zbtb44 Zinc finger and BTB domain-containing protein 44 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
A4II20 egr1 Early growth response protein 1 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q6P882 zbtb8a.2 Zinc finger and BTB domain-containing protein 8A.2 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q567C6 znf367 Zinc finger protein 367 Danio rerio (Zebrafish) (Brachydanio rerio) PR
A7Y7X5 znf711 Zinc finger protein 711 Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MTFPEADILL KSGECAGQTM LDTMEAPGHS RQLLLQLNNQ RTKGFLCDVI IVVQNALFRA
70 80 90 100 110 120
HKNVLAASSA YLKSLVVHDN LLNLDHDMVS PAVFRLVLDF IYTGRLADGA EAAAAAAVAP
130 140 150 160 170 180
GAEPSLGAVL AAASYLQIPD LVALCKKRLK RHGKYCHLRG GGGGGGGYAP YGRPGRGLRA
190 200 210 220 230 240
ATPVIQACYP SPVGPPPPPA AEPPSGPEAA VNTHCAELYA SGPGPAAALC ASERRCSPLC
250 260 270 280 290 300
GLDLSKKSPP GSAAPERPLA ERELPPRPDS PPSAGPAAYK EPPLALPSLP PLPFQKLEEA
310 320 330 340 350 360
APPSDPFRGG SGSPGPEPPG RPDGPSLLYR WMKHEPGLGS YGDELGRERG SPSERCEERG
370 380 390 400 410 420
GDAAVSPGGP PLGLAPPPRY PGSLDGPGAG GDGDDYKSSS EETGSSEDPS PPGGHLEGYP
430 440 450 460 470 480
CPHLAYGEPE SFGDNLYVCI PCGKGFPSSE QLNAHVEAHV EEEEALYGRA EAAEVAAGAA
490 500 510 520 530 540
GLGPPFGGGG DKVAGAPGGL GELLRPYRCA SCDKSYKDPA TLRQHEKTHW LTRPYPCTIC
550 560 570 580 590 600
GKKFTQRGTM TRHMRSHLGL KPFACDACGM RFTRQYRLTE HMRIHSGEKP YECQVCGGKF
610 620 630 640 650 660
AQQRNLISHM KMHAVGGAAG AAGALAGLGG LPGVPGPDGK GKLDFPEGVF AVARLTAEQL
670 680 690 700 710 720
SLKQQDKAAA AELLAQTTHF LHDPKVALES LYPLAKFTAE LGLSPDKAAE VLSQGAHLAA
730
GPDGRTIDRF SPT