Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.6300884G>ACA438367952WFS1c.1125G>A (p.Lys375=)
c.1066G>A
c.1089G>A (p.Lys363=)
c.840G>A (p.Lys280=)
c.748G>A (p.Gly250Ser)
c.722G>A
n.1274G>A
c.1098G>A (p.Lys366=)
ClinVar dbSNP
4g.6300884G>CCA356174228WFS1c.1125G>C (p.Lys375Asn)
c.1066G>C
c.1089G>C (p.Lys363Asn)
c.840G>C (p.Lys280Asn)
c.748G>C (p.Gly250Arg)
c.722G>C
n.1274G>C
c.1098G>C (p.Lys366Asn)
gnomAD v4
4g.6300884G=CA1435772333WFS1c.1125G= (p.Lys375=)
c.1066G=
c.1089G= (p.Lys363=)
c.840G= (p.Lys280=)
c.748G= (p.Gly250=)
c.722G=
n.1274G=
c.1098G= (p.Lys366=)
4g.6300884G>TCA356174229WFS1c.1125G>T (p.Lys375Asn)
c.1066G>T
c.1089G>T (p.Lys363Asn)
c.840G>T (p.Lys280Asn)
c.748G>T (p.Gly250Cys)
c.722G>T
n.1274G>T
c.1098G>T (p.Lys366Asn)
4g.6300885G>ACA356174230WFS1c.1126G>A (p.Val376Met)
c.1067G>A
c.1090G>A (p.Val364Met)
c.841G>A (p.Val281Met)
c.749G>A (p.Gly250Asp)
c.723G>A
n.1275G>A
c.1099G>A (p.Val367Met)
COSMIC
4g.6300885G>CCA356174231WFS1c.1126G>C (p.Val376Leu)
c.1067G>C
c.1090G>C (p.Val364Leu)
c.841G>C (p.Val281Leu)
c.749G>C (p.Gly250Ala)
c.723G>C
n.1275G>C
c.1099G>C (p.Val367Leu)
gnomAD v4
4g.6300885G>TCA356174232WFS1c.1126G>T (p.Val376Leu)
c.1067G>T
c.1090G>T (p.Val364Leu)
c.841G>T (p.Val281Leu)
c.749G>T (p.Gly250Val)
c.723G>T
n.1275G>T
c.1099G>T (p.Val367Leu)
4g.6300886T>ACA356174233WFS1c.1127T>A (p.Val376Glu)
c.1068T>A
c.1091T>A (p.Val364Glu)
c.842T>A (p.Val281Glu)
c.750T>A (p.Gly250=)
c.724T>A
n.1276T>A
c.1100T>A (p.Val367Glu)
4g.6300886T>CCA356174234WFS1c.1127T>C (p.Val376Ala)
c.1068T>C
c.1091T>C (p.Val364Ala)
c.842T>C (p.Val281Ala)
c.750T>C (p.Gly250=)
c.724T>C
n.1276T>C
c.1100T>C (p.Val367Ala)
4g.6300886T>GCA356174235WFS1c.1127T>G (p.Val376Gly)
c.1068T>G
c.1091T>G (p.Val364Gly)
c.842T>G (p.Val281Gly)
c.750T>G (p.Gly250=)
c.724T>G
n.1276T>G
c.1100T>G (p.Val367Gly)
4g.6300887G>ACA438367957WFS1c.1128G>A (p.Val376=)
c.1069G>A
c.1092G>A (p.Val364=)
c.843G>A (p.Val281=)
c.751G>A (p.Val251Ile)
c.725G>A
n.1277G>A
c.1101G>A (p.Val367=)
4g.6300887G>CCA438367955WFS1c.1128G>C (p.Val376=)
c.1069G>C
c.1092G>C (p.Val364=)
c.843G>C (p.Val281=)
c.751G>C (p.Val251Leu)
c.725G>C
n.1277G>C
c.1101G>C (p.Val367=)
4g.6300887G>TCA438367954WFS1c.1128G>T (p.Val376=)
c.1069G>T
c.1092G>T (p.Val364=)
c.843G>T (p.Val281=)
c.751G>T (p.Val251Phe)
c.725G>T
n.1277G>T
c.1101G>T (p.Val367=)
4g.6300888T>ACA356174236WFS1c.1129T>A (p.Phe377Ile)
c.1070T>A
c.1093T>A (p.Phe365Ile)
c.844T>A (p.Phe282Ile)
c.752T>A (p.Val251Asp)
c.726T>A
n.1278T>A
c.1102T>A (p.Phe368Ile)
4g.6300888T>CCA356174237WFS1c.1129T>C (p.Phe377Leu)
c.1070T>C
c.1093T>C (p.Phe365Leu)
c.844T>C (p.Phe282Leu)
c.752T>C (p.Val251Ala)
c.726T>C
n.1278T>C
c.1102T>C (p.Phe368Leu)
dbSNP gnomAD v2 gnomAD v4
4g.6300888T>GCA91796227WFS1c.1129T>G (p.Phe377Val)
c.1070T>G
c.1093T>G (p.Phe365Val)
c.844T>G (p.Phe282Val)
c.752T>G (p.Val251Gly)
c.726T>G
n.1278T>G
c.1102T>G (p.Phe368Val)
dbSNP gnomAD v4
4g.6300888T=CA1435772335WFS1c.1129T= (p.Phe377=)
c.1070T=
c.1093T= (p.Phe365=)
c.844T= (p.Phe282=)
c.752T= (p.Val251=)
c.726T=
n.1278T=
c.1102T= (p.Phe368=)
4g.6300889T>ACA356174241WFS1c.1130T>A (p.Phe377Tyr)
c.1071T>A
c.1094T>A (p.Phe365Tyr)
c.845T>A (p.Phe282Tyr)
c.753T>A (p.Val251=)
c.727T>A
n.1279T>A
c.1103T>A (p.Phe368Tyr)
4g.6300889T>CCA356174242WFS1c.1130T>C (p.Phe377Ser)
c.1071T>C
c.1094T>C (p.Phe365Ser)
c.845T>C (p.Phe282Ser)
c.753T>C (p.Val251=)
c.727T>C
n.1279T>C
c.1103T>C (p.Phe368Ser)
ClinVar gnomAD v4
4g.6300889T>GCA356174239WFS1c.1130T>G (p.Phe377Cys)
c.1071T>G
c.1094T>G (p.Phe365Cys)
c.845T>G (p.Phe282Cys)
c.753T>G (p.Val251=)
c.727T>G
n.1279T>G
c.1103T>G (p.Phe368Cys)
4g.6300890C>ACA356174244WFS1c.1131C>A (p.Phe377Leu)
c.1072C>A
c.1095C>A (p.Phe365Leu)
c.846C>A (p.Phe282Leu)
c.754C>A (p.Pro252Thr)
c.728C>A
n.1280C>A
c.1104C>A (p.Phe368Leu)
4g.6300890C>GCA356174243WFS1c.1131C>G (p.Phe377Leu)
c.1072C>G
c.1095C>G (p.Phe365Leu)
c.846C>G (p.Phe282Leu)
c.754C>G (p.Pro252Ala)
c.728C>G
n.1280C>G
c.1104C>G (p.Phe368Leu)
4g.6300890C>TCA438367962WFS1c.1131C>T (p.Phe377=)
c.1072C>T
c.1095C>T (p.Phe365=)
c.846C>T (p.Phe282=)
c.754C>T (p.Pro252Ser)
c.728C>T
n.1280C>T
c.1104C>T (p.Phe368=)
4g.6300891C>ACA356174246WFS1c.1132C>A (p.Gln378Lys)
c.1073C>A
c.1096C>A (p.Gln366Lys)
c.847C>A (p.Gln283Lys)
c.755C>A (p.Pro252Gln)
c.729C>A
n.1281C>A
c.1105C>A (p.Gln369Lys)
4g.6300891C=CA1435772337WFS1c.1132C= (p.Gln378=)
c.1073C=
c.1096C= (p.Gln366=)
c.847C= (p.Gln283=)
c.755C= (p.Pro252=)
c.729C=
n.1281C=
c.1105C= (p.Gln369=)
4g.6300891C>GCA356174245WFS1c.1132C>G (p.Gln378Glu)
c.1073C>G
c.1096C>G (p.Gln366Glu)
c.847C>G (p.Gln283Glu)
c.755C>G (p.Pro252Arg)
c.729C>G
n.1281C>G
c.1105C>G (p.Gln369Glu)
4g.6300891C>TCA2839217WFS1c.1132C>T (p.Gln378Ter)
c.1073C>T
c.1096C>T (p.Gln366Ter)
c.847C>T (p.Gln283Ter)
c.755C>T (p.Pro252Leu)
c.729C>T
n.1281C>T
c.1105C>T (p.Gln369Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300892A>CCA356174247WFS1c.1133A>C (p.Gln378Pro)
c.1074A>C
c.1097A>C (p.Gln366Pro)
c.848A>C (p.Gln283Pro)
c.756A>C (p.Pro252=)
c.730A>C
n.1282A>C
c.1106A>C (p.Gln369Pro)
4g.6300892A>GCA356174248WFS1c.1133A>G (p.Gln378Arg)
c.1074A>G
c.1097A>G (p.Gln366Arg)
c.848A>G (p.Gln283Arg)
c.756A>G (p.Pro252=)
c.730A>G
n.1282A>G
c.1106A>G (p.Gln369Arg)
4g.6300892A>TCA356174249WFS1c.1133A>T (p.Gln378Leu)
c.1074A>T
c.1097A>T (p.Gln366Leu)
c.848A>T (p.Gln283Leu)
c.756A>T (p.Pro252=)
c.730A>T
n.1282A>T
c.1106A>T (p.Gln369Leu)
4g.6300892_6300902dupCA2586973607WFS1c.1133_1143dup (p.Ala382ArgfsTer?)
c.1074_1084dup
c.1097_1107dup (p.Ala370ArgfsTer?)
c.848_858dup (p.Ala287ArgfsTer?)
c.756_766dup (p.Gly256GlufsTer?)
c.730_740dup
n.1282_1292dup
c.1106_1116dup (p.Ala373ArgfsTer?)
4g.6300893G>ACA438367964WFS1c.1134G>A (p.Gln378=)
c.1075G>A
c.1098G>A (p.Gln366=)
c.849G>A (p.Gln283=)
c.757G>A (p.Gly253Arg)
c.731G>A
n.1283G>A
c.1107G>A (p.Gln369=)
4g.6300893G>CCA356174250WFS1c.1134G>C (p.Gln378His)
c.1075G>C
c.1098G>C (p.Gln366His)
c.849G>C (p.Gln283His)
c.757G>C (p.Gly253Arg)
c.731G>C
n.1283G>C
c.1107G>C (p.Gln369His)
4g.6300893G>TCA356174251WFS1c.1134G>T (p.Gln378His)
c.1075G>T
c.1098G>T (p.Gln366His)
c.849G>T (p.Gln283His)
c.757G>T (p.Gly253Ter)
c.731G>T
n.1283G>T
c.1107G>T (p.Gln369His)
gnomAD v4
4g.6300894G>ACA10618995WFS1c.1135G>A (p.Asp379Asn)
c.1076G>A
c.1099G>A (p.Asp367Asn)
c.850G>A (p.Asp284Asn)
c.758G>A (p.Gly253Glu)
c.732G>A
n.1284G>A
c.1108G>A (p.Asp370Asn)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6300894G>CCA356174252WFS1c.1135G>C (p.Asp379His)
c.1076G>C
c.1099G>C (p.Asp367His)
c.850G>C (p.Asp284His)
c.758G>C (p.Gly253Ala)
c.732G>C
n.1284G>C
c.1108G>C (p.Asp370His)
4g.6300894G=CA1435772339WFS1c.1135G= (p.Asp379=)
c.1076G=
c.1099G= (p.Asp367=)
c.850G= (p.Asp284=)
c.758G= (p.Gly253=)
c.732G=
n.1284G=
c.1108G= (p.Asp370=)
4g.6300894G>TCA356174253WFS1c.1135G>T (p.Asp379Tyr)
c.1076G>T
c.1099G>T (p.Asp367Tyr)
c.850G>T (p.Asp284Tyr)
c.758G>T (p.Gly253Val)
c.732G>T
n.1284G>T
c.1108G>T (p.Asp370Tyr)
ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6300895A=CA1435772342WFS1c.1136A= (p.Asp379=)
c.1077A=
c.1100A= (p.Asp367=)
c.851A= (p.Asp284=)
c.759A= (p.Gly253=)
c.733A=
n.1285A=
c.1109A= (p.Asp370=)
4g.6300895A>CCA356174254WFS1c.1136A>C (p.Asp379Ala)
c.1077A>C
c.1100A>C (p.Asp367Ala)
c.851A>C (p.Asp284Ala)
c.759A>C (p.Gly253=)
c.733A>C
n.1285A>C
c.1109A>C (p.Asp370Ala)
4g.6300895A>GCA2839218WFS1c.1136A>G (p.Asp379Gly)
c.1077A>G
c.1100A>G (p.Asp367Gly)
c.851A>G (p.Asp284Gly)
c.759A>G (p.Gly253=)
c.733A>G
n.1285A>G
c.1109A>G (p.Asp370Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300895A>TCA356174255WFS1c.1136A>T (p.Asp379Val)
c.1077A>T
c.1100A>T (p.Asp367Val)
c.851A>T (p.Asp284Val)
c.759A>T (p.Gly253=)
c.733A>T
n.1285A>T
c.1109A>T (p.Asp370Val)
4g.6300896C>ACA356174256WFS1c.1137C>A (p.Asp379Glu)
c.1078C>A
c.1101C>A (p.Asp367Glu)
c.852C>A (p.Asp284Glu)
c.760C>A (p.Gln254Lys)
c.734C>A
n.1286C>A
c.1110C>A (p.Asp370Glu)
4g.6300896C=CA1435772344WFS1c.1137C= (p.Asp379=)
c.1078C=
c.1101C= (p.Asp367=)
c.852C= (p.Asp284=)
c.760C= (p.Gln254=)
c.734C=
n.1286C=
c.1110C= (p.Asp370=)
4g.6300896C>GCA356174257WFS1c.1137C>G (p.Asp379Glu)
c.1078C>G
c.1101C>G (p.Asp367Glu)
c.852C>G (p.Asp284Glu)
c.760C>G (p.Gln254Glu)
c.734C>G
n.1286C>G
c.1110C>G (p.Asp370Glu)
ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6300896C>TCA438367969WFS1c.1137C>T (p.Asp379=)
c.1078C>T
c.1101C>T (p.Asp367=)
c.852C>T (p.Asp284=)
c.760C>T (p.Gln254Ter)
c.734C>T
n.1286C>T
c.1110C>T (p.Asp370=)
dbSNP gnomAD v4
4g.6300897A>CCA356174258WFS1c.1138A>C (p.Ser380Arg)
c.1079A>C
c.1102A>C (p.Ser368Arg)
c.853A>C (p.Ser285Arg)
c.761A>C (p.Gln254Pro)
c.735A>C
n.1287A>C
c.1111A>C (p.Ser371Arg)
4g.6300897A>GCA356174259WFS1c.1138A>G (p.Ser380Gly)
c.1079A>G
c.1102A>G (p.Ser368Gly)
c.853A>G (p.Ser285Gly)
c.761A>G (p.Gln254Arg)
c.735A>G
n.1287A>G
c.1111A>G (p.Ser371Gly)
ClinVar
4g.6300897A>TCA356174260WFS1c.1138A>T (p.Ser380Cys)
c.1079A>T
c.1102A>T (p.Ser368Cys)
c.853A>T (p.Ser285Cys)
c.761A>T (p.Gln254Leu)
c.735A>T
n.1287A>T
c.1111A>T (p.Ser371Cys)
4g.6300898G>ACA136326WFS1c.1139G>A (p.Ser380Asn)
c.1080G>A
c.1103G>A (p.Ser368Asn)
c.854G>A (p.Ser285Asn)
c.762G>A (p.Gln254=)
c.736G>A
n.1288G>A
c.1112G>A (p.Ser371Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300898G>CCA356174261WFS1c.1139G>C (p.Ser380Thr)
c.1080G>C
c.1103G>C (p.Ser368Thr)
c.854G>C (p.Ser285Thr)
c.762G>C (p.Gln254His)
c.736G>C
n.1288G>C
c.1112G>C (p.Ser371Thr)
dbSNP gnomAD v4
4g.6300898G=CA1435772347WFS1c.1139G= (p.Ser380=)
c.1080G=
c.1103G= (p.Ser368=)
c.854G= (p.Ser285=)
c.762G= (p.Gln254=)
c.736G=
n.1288G=
c.1112G= (p.Ser371=)
4g.6300898G>TCA356174262WFS1c.1139G>T (p.Ser380Ile)
c.1080G>T
c.1103G>T (p.Ser368Ile)
c.854G>T (p.Ser285Ile)
c.762G>T (p.Gln254His)
c.736G>T
n.1288G>T
c.1112G>T (p.Ser371Ile)
4g.6300900_6300904dupCA2586973608WFS1c.1141_1145dup (p.Trp383ArgfsTer?)
c.1082_1086dup
c.1105_1109dup (p.Trp371ArgfsTer?)
c.856_860dup (p.Trp288ArgfsTer?)
c.764_768dup (p.Leu257LysfsTer?)
c.738_742dup
n.1290_1294dup
c.1114_1118dup (p.Trp374ArgfsTer?)
4g.6300899C>ACA356174263WFS1c.1140C>A (p.Ser380Arg)
c.1081C>A
c.1104C>A (p.Ser368Arg)
c.855C>A (p.Ser285Arg)
c.763C>A (p.Gln255Lys)
c.737C>A
n.1289C>A
c.1113C>A (p.Ser371Arg)
4g.6300899C=CA1435772349WFS1c.1140C= (p.Ser380=)
c.1081C=
c.1104C= (p.Ser368=)
c.855C= (p.Ser285=)
c.763C= (p.Gln255=)
c.737C=
n.1289C=
c.1113C= (p.Ser371=)
4g.6300899C>GCA2839219WFS1c.1140C>G (p.Ser380Arg)
c.1081C>G
c.1104C>G (p.Ser368Arg)
c.855C>G (p.Ser285Arg)
c.763C>G (p.Gln255Glu)
c.737C>G
n.1289C>G
c.1113C>G (p.Ser371Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300899C>TCA438367971WFS1c.1140C>T (p.Ser380=)
c.1081C>T
c.1104C>T (p.Ser368=)
c.855C>T (p.Ser285=)
c.763C>T (p.Gln255Ter)
c.737C>T
n.1289C>T
c.1113C>T (p.Ser371=)
4g.6300899_6300900insTCA549707897WFS1c.1140_1141insT (p.Lys381Ter)
c.1081_1082insT
c.1104_1105insT (p.Lys369Ter)
c.855_856insT (p.Lys286Ter)
c.763_764insT (p.Gln255LeufsTer?)
c.737_738insT
n.1289_1290insT
c.1113_1114insT (p.Lys372Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6300900A>CCA356174264WFS1c.1141A>C (p.Lys381Gln)
c.1082A>C
c.1105A>C (p.Lys369Gln)
c.856A>C (p.Lys286Gln)
c.764A>C (p.Gln255Pro)
c.738A>C
n.1290A>C
c.1114A>C (p.Lys372Gln)
4g.6300900A>GCA356174265WFS1c.1141A>G (p.Lys381Glu)
c.1082A>G
c.1105A>G (p.Lys369Glu)
c.856A>G (p.Lys286Glu)
c.764A>G (p.Gln255Arg)
c.738A>G
n.1290A>G
c.1114A>G (p.Lys372Glu)
4g.6300900A>TCA356174266WFS1c.1141A>T (p.Lys381Ter)
c.1082A>T
c.1105A>T (p.Lys369Ter)
c.856A>T (p.Lys286Ter)
c.764A>T (p.Gln255Leu)
c.738A>T
n.1290A>T
c.1114A>T (p.Lys372Ter)
4g.6300901A=CA1435772352WFS1c.1142A= (p.Lys381=)
c.1083A=
c.1106A= (p.Lys369=)
c.857A= (p.Lys286=)
c.765A= (p.Gln255=)
c.739A=
n.1291A=
c.1115A= (p.Lys372=)
4g.6300901A>CCA322697WFS1c.1142A>C (p.Lys381Thr)
c.1083A>C
c.1106A>C (p.Lys369Thr)
c.857A>C (p.Lys286Thr)
c.765A>C (p.Gln255His)
c.739A>C
n.1291A>C
c.1115A>C (p.Lys372Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300901A>GCA356174268WFS1c.1142A>G (p.Lys381Arg)
c.1083A>G
c.1106A>G (p.Lys369Arg)
c.857A>G (p.Lys286Arg)
c.765A>G (p.Gln255=)
c.739A>G
n.1291A>G
c.1115A>G (p.Lys372Arg)
4g.6300901A>TCA356174267WFS1c.1142A>T (p.Lys381Met)
c.1083A>T
c.1106A>T (p.Lys369Met)
c.857A>T (p.Lys286Met)
c.765A>T (p.Gln255His)
c.739A>T
n.1291A>T
c.1115A>T (p.Lys372Met)
dbSNP gnomAD v3 gnomAD v4
4g.6300902G>ACA438367973WFS1c.1143G>A (p.Lys381=)
c.1084G>A
c.1107G>A (p.Lys369=)
c.858G>A (p.Lys286=)
c.766G>A (p.Gly256Ser)
c.740G>A
n.1292G>A
c.1116G>A (p.Lys372=)
gnomAD v4
4g.6300902G>CCA356174269WFS1c.1143G>C (p.Lys381Asn)
c.1084G>C
c.1107G>C (p.Lys369Asn)
c.858G>C (p.Lys286Asn)
c.766G>C (p.Gly256Arg)
c.740G>C
n.1292G>C
c.1116G>C (p.Lys372Asn)
4g.6300902G>TCA356174270WFS1c.1143G>T (p.Lys381Asn)
c.1084G>T
c.1107G>T (p.Lys369Asn)
c.858G>T (p.Lys286Asn)
c.766G>T (p.Gly256Cys)
c.740G>T
n.1292G>T
c.1116G>T (p.Lys372Asn)
4g.6300902_6300903insACA2499217322WFS1c.1143_1144insA (p.Ala382SerfsTer?)
c.1084_1085insA
c.1107_1108insA (p.Ala370SerfsTer?)
c.858_859insA (p.Ala287SerfsTer?)
c.766_767insA (p.Gly256GlufsTer?)
c.740_741insA
n.1292_1293insA
c.1116_1117insA (p.Ala373SerfsTer?)
ClinVar dbSNP gnomAD v4
4g.6300903G>ACA2839220WFS1c.1144G>A (p.Ala382Thr)
c.1085G>A
c.1108G>A (p.Ala370Thr)
c.859G>A (p.Ala287Thr)
c.767G>A (p.Gly256Asp)
c.741G>A
n.1293G>A
c.1117G>A (p.Ala373Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300903G>CCA356174271WFS1c.1144G>C (p.Ala382Pro)
c.1085G>C
c.1108G>C (p.Ala370Pro)
c.859G>C (p.Ala287Pro)
c.767G>C (p.Gly256Ala)
c.741G>C
n.1293G>C
c.1117G>C (p.Ala373Pro)
4g.6300903G=CA1435772355WFS1c.1144G= (p.Ala382=)
c.1085G=
c.1108G= (p.Ala370=)
c.859G= (p.Ala287=)
c.767G= (p.Gly256=)
c.741G=
n.1293G=
c.1117G= (p.Ala373=)
4g.6300903G>TCA356174272WFS1c.1144G>T (p.Ala382Ser)
c.1085G>T
c.1108G>T (p.Ala370Ser)
c.859G>T (p.Ala287Ser)
c.767G>T (p.Gly256Val)
c.741G>T
n.1293G>T
c.1117G>T (p.Ala373Ser)
gnomAD v4
4g.6300904C>ACA356174275WFS1c.1145C>A (p.Ala382Asp)
c.1086C>A
c.1109C>A (p.Ala370Asp)
c.860C>A (p.Ala287Asp)
c.768C>A (p.Gly256=)
c.742C>A
n.1294C>A
c.1118C>A (p.Ala373Asp)
dbSNP gnomAD v2
4g.6300904C=CA1435772357WFS1c.1145C= (p.Ala382=)
c.1086C=
c.1109C= (p.Ala370=)
c.860C= (p.Ala287=)
c.768C= (p.Gly256=)
c.742C=
n.1294C=
c.1118C= (p.Ala373=)
4g.6300904C>GCA356174274WFS1c.1145C>G (p.Ala382Gly)
c.1086C>G
c.1109C>G (p.Ala370Gly)
c.860C>G (p.Ala287Gly)
c.768C>G (p.Gly256=)
c.742C>G
n.1294C>G
c.1118C>G (p.Ala373Gly)
gnomAD v4
4g.6300904C>TCA356174273WFS1c.1145C>T (p.Ala382Val)
c.1086C>T
c.1109C>T (p.Ala370Val)
c.860C>T (p.Ala287Val)
c.768C>T (p.Gly256=)
c.742C>T
n.1294C>T
c.1118C>T (p.Ala373Val)
ClinVar dbSNP
4g.6300905C>ACA438367977WFS1c.1146C>A (p.Ala382=)
c.1087C>A
c.1110C>A (p.Ala370=)
c.861C>A (p.Ala287=)
c.769C>A (p.Leu257Met)
c.743C>A
n.1295C>A
c.1119C>A (p.Ala373=)
4g.6300905C=CA1435772359WFS1c.1146C= (p.Ala382=)
c.1087C=
c.1110C= (p.Ala370=)
c.861C= (p.Ala287=)
c.769C= (p.Leu257=)
c.743C=
n.1295C=
c.1119C= (p.Ala373=)
4g.6300905C>GCA438367978WFS1c.1146C>G (p.Ala382=)
c.1087C>G
c.1110C>G (p.Ala370=)
c.861C>G (p.Ala287=)
c.769C>G (p.Leu257Val)
c.743C>G
n.1295C>G
c.1119C>G (p.Ala373=)
ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6300905C>TCA91796228WFS1c.1146C>T (p.Ala382=)
c.1087C>T
c.1110C>T (p.Ala370=)
c.861C>T (p.Ala287=)
c.769C>T (p.Leu257=)
c.743C>T
n.1295C>T
c.1119C>T (p.Ala373=)
ClinVar dbSNP
4g.6300906T>ACA356174276WFS1c.1147T>A (p.Trp383Arg)
c.1088T>A
c.1111T>A (p.Trp371Arg)
c.862T>A (p.Trp288Arg)
c.770T>A (p.Leu257Gln)
c.744T>A
n.1296T>A
c.1120T>A (p.Trp374Arg)
4g.6300906T>CCA356174277WFS1c.1147T>C (p.Trp383Arg)
c.1088T>C
c.1111T>C (p.Trp371Arg)
c.862T>C (p.Trp288Arg)
c.770T>C (p.Leu257Pro)
c.744T>C
n.1296T>C
c.1120T>C (p.Trp374Arg)
4g.6300906T>GCA356174278WFS1c.1147T>G (p.Trp383Gly)
c.1088T>G
c.1111T>G (p.Trp371Gly)
c.862T>G (p.Trp288Gly)
c.770T>G (p.Leu257Arg)
c.744T>G
n.1296T>G
c.1120T>G (p.Trp374Gly)
ClinVar dbSNP gnomAD v4
4g.6300907G>ACA356174279WFS1c.1148G>A (p.Trp383Ter)
c.1089G>A
c.1112G>A (p.Trp371Ter)
c.863G>A (p.Trp288Ter)
c.771G>A (p.Leu257=)
c.745G>A
n.1297G>A
c.1121G>A (p.Trp374Ter)
ClinVar dbSNP
4g.6300907G>CCA356174280WFS1c.1148G>C (p.Trp383Ser)
c.1089G>C
c.1112G>C (p.Trp371Ser)
c.863G>C (p.Trp288Ser)
c.771G>C (p.Leu257=)
c.745G>C
n.1297G>C
c.1121G>C (p.Trp374Ser)
dbSNP
4g.6300907G=CA1435772361WFS1c.1148G= (p.Trp383=)
c.1089G=
c.1112G= (p.Trp371=)
c.863G= (p.Trp288=)
c.771G= (p.Leu257=)
c.745G=
n.1297G=
c.1121G= (p.Trp374=)
4g.6300907G>TCA356174281WFS1c.1148G>T (p.Trp383Leu)
c.1089G>T
c.1112G>T (p.Trp371Leu)
c.863G>T (p.Trp288Leu)
c.771G>T (p.Leu257=)
c.745G>T
n.1297G>T
c.1121G>T (p.Trp374Leu)
4g.6300908G>ACA356174282WFS1c.1149G>A (p.Trp383Ter)
c.1090G>A
c.1113G>A (p.Trp371Ter)
c.864G>A (p.Trp288Ter)
c.772G>A (p.Gly258Arg)
c.746G>A
n.1298G>A
c.1122G>A (p.Trp374Ter)
dbSNP gnomAD v2 gnomAD v4
4g.6300908G>CCA356174284WFS1c.1149G>C (p.Trp383Cys)
c.1090G>C
c.1113G>C (p.Trp371Cys)
c.864G>C (p.Trp288Cys)
c.772G>C (p.Gly258Arg)
c.746G>C
n.1298G>C
c.1122G>C (p.Trp374Cys)
4g.6300908G=CA1435772363WFS1c.1149G= (p.Trp383=)
c.1090G=
c.1113G= (p.Trp371=)
c.864G= (p.Trp288=)
c.772G= (p.Gly258=)
c.746G=
n.1298G=
c.1122G= (p.Trp374=)
4g.6300908G>TCA356174283WFS1c.1149G>T (p.Trp383Cys)
c.1090G>T
c.1113G>T (p.Trp371Cys)
c.864G>T (p.Trp288Cys)
c.772G>T (p.Gly258Ter)
c.746G>T
n.1298G>T
c.1122G>T (p.Trp374Cys)
COSMIC
4g.6300909G>ACA356174285WFS1c.1150G>A (p.Glu384Lys)
c.1091G>A
c.1114G>A (p.Glu372Lys)
c.865G>A (p.Glu289Lys)
c.773G>A (p.Gly258Glu)
c.747G>A
n.1299G>A
c.1123G>A (p.Glu375Lys)
4g.6300909G>CCA356174286WFS1c.1150G>C (p.Glu384Gln)
c.1091G>C
c.1114G>C (p.Glu372Gln)
c.865G>C (p.Glu289Gln)
c.773G>C (p.Gly258Ala)
c.747G>C
n.1299G>C
c.1123G>C (p.Glu375Gln)
dbSNP gnomAD v4
4g.6300909G=CA1435772366WFS1c.1150G= (p.Glu384=)
c.1091G=
c.1114G= (p.Glu372=)
c.865G= (p.Glu289=)
c.773G= (p.Gly258=)
c.747G=
n.1299G=
c.1123G= (p.Glu375=)
4g.6300909G>TCA356174287WFS1c.1150G>T (p.Glu384Ter)
c.1091G>T
c.1114G>T (p.Glu372Ter)
c.865G>T (p.Glu289Ter)
c.773G>T (p.Gly258Val)
c.747G>T
n.1299G>T
c.1123G>T (p.Glu375Ter)
4g.6300910A=CA1435772367WFS1c.1151A= (p.Glu384=)
c.1092A=
c.1115A= (p.Glu372=)
c.866A= (p.Glu289=)
c.774A= (p.Gly258=)
c.748A=
n.1300A=
c.1124A= (p.Glu375=)
4g.6300910A>CCA356174288WFS1c.1151A>C (p.Glu384Ala)
c.1092A>C
c.1115A>C (p.Glu372Ala)
c.866A>C (p.Glu289Ala)
c.774A>C (p.Gly258=)
c.748A>C
n.1300A>C
c.1124A>C (p.Glu375Ala)
dbSNP
4g.6300910A>GCA356174289WFS1c.1151A>G (p.Glu384Gly)
c.1092A>G
c.1115A>G (p.Glu372Gly)
c.866A>G (p.Glu289Gly)
c.774A>G (p.Gly258=)
c.748A>G
n.1300A>G
c.1124A>G (p.Glu375Gly)
4g.6300910A>TCA356174290WFS1c.1151A>T (p.Glu384Val)
c.1092A>T
c.1115A>T (p.Glu372Val)
c.866A>T (p.Glu289Val)
c.774A>T (p.Gly258=)
c.748A>T
n.1300A>T
c.1124A>T (p.Glu375Val)
4g.6300911G>ACA438367980WFS1c.1152G>A (p.Glu384=)
c.1093G>A
c.1116G>A (p.Glu372=)
c.867G>A (p.Glu289=)
c.775G>A (p.Glu259Lys)
c.749G>A
n.1301G>A
c.1125G>A (p.Glu375=)
4g.6300911G>CCA356174291WFS1c.1152G>C (p.Glu384Asp)
c.1093G>C
c.1116G>C (p.Glu372Asp)
c.867G>C (p.Glu289Asp)
c.775G>C (p.Glu259Gln)
c.749G>C
n.1301G>C
c.1125G>C (p.Glu375Asp)
4g.6300911G>TCA356174292WFS1c.1152G>T (p.Glu384Asp)
c.1093G>T
c.1116G>T (p.Glu372Asp)
c.867G>T (p.Glu289Asp)
c.775G>T (p.Glu259Ter)
c.749G>T
n.1301G>T
c.1125G>T (p.Glu375Asp)
4g.6300912A=CA1435772369WFS1c.1153A= (p.Asn385=)
c.1094A=
c.1117A= (p.Asn373=)
c.868A= (p.Asn290=)
c.776A= (p.Glu259=)
c.750A=
n.1302A=
c.1126A= (p.Asn376=)
4g.6300912A>CCA91796229WFS1c.1153A>C (p.Asn385His)
c.1094A>C
c.1117A>C (p.Asn373His)
c.868A>C (p.Asn290His)
c.776A>C (p.Glu259Ala)
c.750A>C
n.1302A>C
c.1126A>C (p.Asn376His)
dbSNP gnomAD v4
4g.6300912A>GCA356174293WFS1c.1153A>G (p.Asn385Asp)
c.1094A>G
c.1117A>G (p.Asn373Asp)
c.868A>G (p.Asn290Asp)
c.776A>G (p.Glu259Gly)
c.750A>G
n.1302A>G
c.1126A>G (p.Asn376Asp)
dbSNP gnomAD v4
4g.6300912A>TCA356174294WFS1c.1153A>T (p.Asn385Tyr)
c.1094A>T
c.1117A>T (p.Asn373Tyr)
c.868A>T (p.Asn290Tyr)
c.776A>T (p.Glu259Val)
c.750A>T
n.1302A>T
c.1126A>T (p.Asn376Tyr)
4g.6300913A=CA1435772370WFS1c.1154A= (p.Asn385=)
c.1095A=
c.1118A= (p.Asn373=)
c.869A= (p.Asn290=)
c.777A= (p.Glu259=)
c.751A=
n.1303A=
c.1127A= (p.Asn376=)
4g.6300913A>CCA356174296WFS1c.1154A>C (p.Asn385Thr)
c.1095A>C
c.1118A>C (p.Asn373Thr)
c.869A>C (p.Asn290Thr)
c.777A>C (p.Glu259Asp)
c.751A>C
n.1303A>C
c.1127A>C (p.Asn376Thr)
4g.6300913A>GCA2839221WFS1c.1154A>G (p.Asn385Ser)
c.1095A>G
c.1118A>G (p.Asn373Ser)
c.869A>G (p.Asn290Ser)
c.777A>G (p.Glu259=)
c.751A>G
n.1303A>G
c.1127A>G (p.Asn376Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300913A>TCA356174295WFS1c.1154A>T (p.Asn385Ile)
c.1095A>T
c.1118A>T (p.Asn373Ile)
c.869A>T (p.Asn290Ile)
c.777A>T (p.Glu259Asp)
c.751A>T
n.1303A>T
c.1127A>T (p.Asn376Ile)
4g.6300914C>ACA2839223WFS1c.1155C>A (p.Asn385Lys)
c.1096C>A
c.1119C>A (p.Asn373Lys)
c.870C>A (p.Asn290Lys)
c.778C>A (p.Leu260Ile)
c.752C>A
n.1304C>A
c.1128C>A (p.Asn376Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300914C=CA1435772372WFS1c.1155C= (p.Asn385=)
c.1096C=
c.1119C= (p.Asn373=)
c.870C= (p.Asn290=)
c.778C= (p.Leu260=)
c.752C=
n.1304C=
c.1128C= (p.Asn376=)
4g.6300914C>GCA2839222WFS1c.1155C>G (p.Asn385Lys)
c.1096C>G
c.1119C>G (p.Asn373Lys)
c.870C>G (p.Asn290Lys)
c.778C>G (p.Leu260Val)
c.752C>G
n.1304C>G
c.1128C>G (p.Asn376Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300914C>TCA438367984WFS1c.1155C>T (p.Asn385=)
c.1096C>T
c.1119C>T (p.Asn373=)
c.870C>T (p.Asn290=)
c.778C>T (p.Leu260Phe)
c.752C>T
n.1304C>T
c.1128C>T (p.Asn376=)
4g.6300915T>ACA356174297WFS1c.1156T>A (p.Phe386Ile)
c.1097T>A
c.1120T>A (p.Phe374Ile)
c.871T>A (p.Phe291Ile)
c.779T>A (p.Leu260His)
c.753T>A
n.1305T>A
c.1129T>A (p.Phe377Ile)
4g.6300915T>CCA356174298WFS1c.1156T>C (p.Phe386Leu)
c.1097T>C
c.1120T>C (p.Phe374Leu)
c.871T>C (p.Phe291Leu)
c.779T>C (p.Leu260Pro)
c.753T>C
n.1305T>C
c.1129T>C (p.Phe377Leu)
4g.6300915T>GCA356174299WFS1c.1156T>G (p.Phe386Val)
c.1097T>G
c.1120T>G (p.Phe374Val)
c.871T>G (p.Phe291Val)
c.779T>G (p.Leu260Arg)
c.753T>G
n.1305T>G
c.1129T>G (p.Phe377Val)
4g.6300916T>ACA356174300WFS1c.1157T>A (p.Phe386Tyr)
c.1098T>A
c.1121T>A (p.Phe374Tyr)
c.872T>A (p.Phe291Tyr)
c.780T>A (p.Leu260=)
c.754T>A
n.1306T>A
c.1130T>A (p.Phe377Tyr)
4g.6300916T>CCA356174301WFS1c.1157T>C (p.Phe386Ser)
c.1098T>C
c.1121T>C (p.Phe374Ser)
c.872T>C (p.Phe291Ser)
c.780T>C (p.Leu260=)
c.754T>C
n.1306T>C
c.1130T>C (p.Phe377Ser)
4g.6300916T>GCA356174302WFS1c.1157T>G (p.Phe386Cys)
c.1098T>G
c.1121T>G (p.Phe374Cys)
c.872T>G (p.Phe291Cys)
c.780T>G (p.Leu260=)
c.754T>G
n.1306T>G
c.1130T>G (p.Phe377Cys)
4g.6300917C>ACA356174303WFS1c.1158C>A (p.Phe386Leu)
c.1099C>A
c.1122C>A (p.Phe374Leu)
c.873C>A (p.Phe291Leu)
c.781C>A (p.Pro261Thr)
c.755C>A
n.1307C>A
c.1131C>A (p.Phe377Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6300917C=CA1435772374WFS1c.1158C= (p.Phe386=)
c.1099C=
c.1122C= (p.Phe374=)
c.873C= (p.Phe291=)
c.781C= (p.Pro261=)
c.755C=
n.1307C=
c.1131C= (p.Phe377=)
4g.6300917C>GCA356174304WFS1c.1158C>G (p.Phe386Leu)
c.1099C>G
c.1122C>G (p.Phe374Leu)
c.873C>G (p.Phe291Leu)
c.781C>G (p.Pro261Ala)
c.755C>G
n.1307C>G
c.1131C>G (p.Phe377Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6300917C>TCA438367986WFS1c.1158C>T (p.Phe386=)
c.1099C>T
c.1122C>T (p.Phe374=)
c.873C>T (p.Phe291=)
c.781C>T (p.Pro261Ser)
c.755C>T
n.1307C>T
c.1131C>T (p.Phe377=)
4g.6300918C>ACA2839224WFS1c.1159C>A (p.Arg387Ser)
c.1100C>A
c.1123C>A (p.Arg375Ser)
c.874C>A (p.Arg292Ser)
c.782C>A (p.Pro261Gln)
n.1308C>A
c.1132C>A (p.Arg378Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300918C=CA1435772377WFS1c.1159C= (p.Arg387=)
c.1100C=
c.1123C= (p.Arg375=)
c.874C= (p.Arg292=)
c.782C= (p.Pro261=)
n.1308C=
c.1132C= (p.Arg378=)
4g.6300918C>GCA356174305WFS1c.1159C>G (p.Arg387Gly)
c.1100C>G
c.1123C>G (p.Arg375Gly)
c.874C>G (p.Arg292Gly)
c.782C>G (p.Pro261Arg)
n.1308C>G
c.1132C>G (p.Arg378Gly)
4g.6300918C>TCA320427WFS1c.1159C>T (p.Arg387Cys)
c.1100C>T
c.1123C>T (p.Arg375Cys)
c.874C>T (p.Arg292Cys)
c.782C>T (p.Pro261Leu)
n.1308C>T
c.1132C>T (p.Arg378Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300919G>ACA2839225WFS1c.1160G>A (p.Arg387His)
c.1101G>A
c.1124G>A (p.Arg375His)
c.875G>A (p.Arg292His)
c.783G>A (p.Pro261=)
n.1309G>A
c.1133G>A (p.Arg378His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300919G>CCA356174306WFS1c.1160G>C (p.Arg387Pro)
c.1101G>C
c.1124G>C (p.Arg375Pro)
c.875G>C (p.Arg292Pro)
c.783G>C (p.Pro261=)
n.1309G>C
c.1133G>C (p.Arg378Pro)
4g.6300919G=CA1435772382WFS1c.1160G= (p.Arg387=)
c.1101G=
c.1124G= (p.Arg375=)
c.875G= (p.Arg292=)
c.783G= (p.Pro261=)
n.1309G=
c.1133G= (p.Arg378=)
4g.6300919G>TCA356174307WFS1c.1160G>T (p.Arg387Leu)
c.1101G>T
c.1124G>T (p.Arg375Leu)
c.875G>T (p.Arg292Leu)
c.783G>T (p.Pro261=)
n.1309G>T
c.1133G>T (p.Arg378Leu)
dbSNP
4g.6300920C>ACA438368073WFS1c.1161C>A (p.Arg387=)
c.1102C>A
c.1125C>A (p.Arg375=)
c.876C>A (p.Arg292=)
c.784C>A (p.His262Asn)
n.1310C>A
c.1134C>A (p.Arg378=)
4g.6300920C=CA1435772387WFS1c.1161C= (p.Arg387=)
c.1102C=
c.1125C= (p.Arg375=)
c.876C= (p.Arg292=)
c.784C= (p.His262=)
n.1310C=
c.1134C= (p.Arg378=)
4g.6300920C>GCA438368074WFS1c.1161C>G (p.Arg387=)
c.1102C>G
c.1125C>G (p.Arg375=)
c.876C>G (p.Arg292=)
c.784C>G (p.His262Asp)
n.1310C>G
c.1134C>G (p.Arg378=)
4g.6300920C>TCA2839226WFS1c.1161C>T (p.Arg387=)
c.1102C>T
c.1125C>T (p.Arg375=)
c.876C>T (p.Arg292=)
c.784C>T (p.His262Tyr)
n.1310C>T
c.1134C>T (p.Arg378=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300921A>CCA356174308WFS1c.1162A>C (p.Thr388Pro)
c.1103A>C
c.1126A>C (p.Thr376Pro)
c.877A>C (p.Thr293Pro)
c.785A>C (p.His262Pro)
n.1311A>C
c.1135A>C (p.Thr379Pro)
4g.6300921A>GCA356174309WFS1c.1162A>G (p.Thr388Ala)
c.1103A>G
c.1126A>G (p.Thr376Ala)
c.877A>G (p.Thr293Ala)
c.785A>G (p.His262Arg)
n.1311A>G
c.1135A>G (p.Thr379Ala)
4g.6300921A>TCA356174310WFS1c.1162A>T (p.Thr388Ser)
c.1103A>T
c.1126A>T (p.Thr376Ser)
c.877A>T (p.Thr293Ser)
c.785A>T (p.His262Leu)
n.1311A>T
c.1135A>T (p.Thr379Ser)
gnomAD v4
4g.6300922C>ACA356174311WFS1c.1163C>A (p.Thr388Asn)
c.1104C>A
c.1127C>A (p.Thr376Asn)
c.878C>A (p.Thr293Asn)
c.786C>A (p.His262Gln)
n.1312C>A
c.1136C>A (p.Thr379Asn)
4g.6300922C=CA1435772390WFS1c.1163C= (p.Thr388=)
c.1104C=
c.1127C= (p.Thr376=)
c.878C= (p.Thr293=)
c.786C= (p.His262=)
n.1312C=
c.1136C= (p.Thr379=)
4g.6300922C>GCA356174312WFS1c.1163C>G (p.Thr388Ser)
c.1104C>G
c.1127C>G (p.Thr376Ser)
c.878C>G (p.Thr293Ser)
c.786C>G (p.His262Gln)
n.1312C>G
c.1136C>G (p.Thr379Ser)
gnomAD v4
4g.6300922C>TCA2839227WFS1c.1163C>T (p.Thr388Ile)
c.1104C>T
c.1127C>T (p.Thr376Ile)
c.878C>T (p.Thr293Ile)
c.786C>T (p.His262=)
n.1312C>T
c.1136C>T (p.Thr379Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300923C>ACA438368078WFS1c.1164C>A (p.Thr388=)
c.1105C>A
c.1128C>A (p.Thr376=)
c.879C>A (p.Thr293=)
c.787C>A (p.Pro263Thr)
n.1313C>A
c.1137C>A (p.Thr379=)
4g.6300923C=CA1435772393WFS1c.1164C= (p.Thr388=)
c.1105C=
c.1128C= (p.Thr376=)
c.879C= (p.Thr293=)
c.787C= (p.Pro263=)
n.1313C=
c.1137C= (p.Thr379=)
4g.6300923C>GCA438368080WFS1c.1164C>G (p.Thr388=)
c.1105C>G
c.1128C>G (p.Thr376=)
c.879C>G (p.Thr293=)
c.787C>G (p.Pro263Ala)
n.1313C>G
c.1137C>G (p.Thr379=)
4g.6300923C>TCA438368081WFS1c.1164C>T (p.Thr388=)
c.1105C>T
c.1128C>T (p.Thr376=)
c.879C>T (p.Thr293=)
c.787C>T (p.Pro263Ser)
n.1313C>T
c.1137C>T (p.Thr379=)
dbSNP gnomAD v2 gnomAD v4
4g.6300924C>ACA356174313WFS1c.1165C>A (p.Leu389Ile)
c.1106C>A
c.1129C>A (p.Leu377Ile)
c.880C>A (p.Leu294Ile)
c.788C>A (p.Pro263His)
n.1314C>A
c.1138C>A (p.Leu380Ile)
4g.6300924C=CA1435772395WFS1c.1165C= (p.Leu389=)
c.1106C=
c.1129C= (p.Leu377=)
c.880C= (p.Leu294=)
c.788C= (p.Pro263=)
n.1314C=
c.1138C= (p.Leu380=)
4g.6300924C>GCA2839228WFS1c.1165C>G (p.Leu389Val)
c.1106C>G
c.1129C>G (p.Leu377Val)
c.880C>G (p.Leu294Val)
c.788C>G (p.Pro263Arg)
n.1314C>G
c.1138C>G (p.Leu380Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300924C>TCA356174314WFS1c.1165C>T (p.Leu389Phe)
c.1106C>T
c.1129C>T (p.Leu377Phe)
c.880C>T (p.Leu294Phe)
c.788C>T (p.Pro263Leu)
n.1314C>T
c.1138C>T (p.Leu380Phe)
4g.6300925T>ACA356174315WFS1c.1166T>A (p.Leu389His)
c.1107T>A
c.1130T>A (p.Leu377His)
c.881T>A (p.Leu294His)
c.789T>A (p.Pro263=)
n.1315T>A
c.1139T>A (p.Leu380His)
4g.6300925T>CCA356174316WFS1c.1166T>C (p.Leu389Pro)
c.1107T>C
c.1130T>C (p.Leu377Pro)
c.881T>C (p.Leu294Pro)
c.789T>C (p.Pro263=)
n.1315T>C
c.1139T>C (p.Leu380Pro)
4g.6300925T>GCA356174317WFS1c.1166T>G (p.Leu389Arg)
c.1107T>G
c.1130T>G (p.Leu377Arg)
c.881T>G (p.Leu294Arg)
c.789T>G (p.Pro263=)
n.1315T>G
c.1139T>G (p.Leu380Arg)
4g.6300926C>ACA438368084WFS1c.1167C>A (p.Leu389=)
c.1108C>A
c.1131C>A (p.Leu377=)
c.882C>A (p.Leu294=)
c.790C>A (p.His264Asn)
n.1316C>A
c.1140C>A (p.Leu380=)
4g.6300926C=CA1435772398WFS1c.1167C= (p.Leu389=)
c.1108C=
c.1131C= (p.Leu377=)
c.882C= (p.Leu294=)
c.790C= (p.His264=)
n.1316C=
c.1140C= (p.Leu380=)
4g.6300926C>GCA438368085WFS1c.1167C>G (p.Leu389=)
c.1108C>G
c.1131C>G (p.Leu377=)
c.882C>G (p.Leu294=)
c.790C>G (p.His264Asp)
n.1316C>G
c.1140C>G (p.Leu380=)
4g.6300926C>TCA438368086WFS1c.1167C>T (p.Leu389=)
c.1108C>T
c.1131C>T (p.Leu377=)
c.882C>T (p.Leu294=)
c.790C>T (p.His264Tyr)
n.1316C>T
c.1140C>T (p.Leu380=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6300927A=CA1435772399WFS1c.1168A= (p.Thr390=)
c.1109A=
c.1132A= (p.Thr378=)
c.883A= (p.Thr295=)
c.791A= (p.His264=)
n.1317A=
c.1141A= (p.Thr381=)
4g.6300927A>CCA356174319WFS1c.1168A>C (p.Thr390Pro)
c.1109A>C
c.1132A>C (p.Thr378Pro)
c.883A>C (p.Thr295Pro)
c.791A>C (p.His264Pro)
n.1317A>C
c.1141A>C (p.Thr381Pro)
gnomAD v4
4g.6300927A>GCA356174318WFS1c.1168A>G (p.Thr390Ala)
c.1109A>G
c.1132A>G (p.Thr378Ala)
c.883A>G (p.Thr295Ala)
c.791A>G (p.His264Arg)
n.1317A>G
c.1141A>G (p.Thr381Ala)
dbSNP gnomAD v2 gnomAD v4
4g.6300927A>TCA2839229WFS1c.1168A>T (p.Thr390Ser)
c.1109A>T
c.1132A>T (p.Thr378Ser)
c.883A>T (p.Thr295Ser)
c.791A>T (p.His264Leu)
n.1317A>T
c.1141A>T (p.Thr381Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300928C>ACA356174320WFS1c.1169C>A (p.Thr390Asn)
c.1110C>A
c.1133C>A (p.Thr378Asn)
c.884C>A (p.Thr295Asn)
c.792C>A (p.His264Gln)
n.1318C>A
c.1142C>A (p.Thr381Asn)
gnomAD v4
4g.6300928C=CA1435772401WFS1c.1169C= (p.Thr390=)
c.1110C=
c.1133C= (p.Thr378=)
c.884C= (p.Thr295=)
c.792C= (p.His264=)
n.1318C=
c.1142C= (p.Thr381=)
4g.6300928C>GCA356174321WFS1c.1169C>G (p.Thr390Ser)
c.1110C>G
c.1133C>G (p.Thr378Ser)
c.884C>G (p.Thr295Ser)
c.792C>G (p.His264Gln)
n.1318C>G
c.1142C>G (p.Thr381Ser)
dbSNP gnomAD v3 gnomAD v4
4g.6300928C>TCA356174322WFS1c.1169C>T (p.Thr390Ile)
c.1110C>T
c.1133C>T (p.Thr378Ile)
c.884C>T (p.Thr295Ile)
c.792C>T (p.His264=)
n.1318C>T
c.1142C>T (p.Thr381Ile)
gnomAD v4
4g.6300929C>ACA136328WFS1c.1170C>A (p.Thr390=)
c.1111C>A
c.1134C>A (p.Thr378=)
c.885C>A (p.Thr295=)
c.793C>A (p.Arg265=)
n.1319C>A
c.1143C>A (p.Thr381=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300929C=CA1435772404WFS1c.1170C= (p.Thr390=)
c.1111C=
c.1134C= (p.Thr378=)
c.885C= (p.Thr295=)
c.793C= (p.Arg265=)
n.1319C=
c.1143C= (p.Thr381=)
4g.6300929C>GCA2839230WFS1c.1170C>G (p.Thr390=)
c.1111C>G
c.1134C>G (p.Thr378=)
c.885C>G (p.Thr295=)
c.793C>G (p.Arg265Gly)
n.1319C>G
c.1143C>G (p.Thr381=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300929C>TCA2839231WFS1c.1170C>T (p.Thr390=)
c.1111C>T
c.1134C>T (p.Thr378=)
c.885C>T (p.Thr295=)
c.793C>T (p.Arg265Ter)
n.1319C>T
c.1143C>T (p.Thr381=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6300930G>ACA319808WFS1c.1171G>A (p.Asp391Asn)
c.1112G>A
c.1135G>A (p.Asp379Asn)
c.886G>A (p.Asp296Asn)
c.794G>A (p.Arg265Gln)
n.1320G>A
c.1144G>A (p.Asp382Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300930G>CCA356174323WFS1c.1171G>C (p.Asp391His)
c.1112G>C
c.1135G>C (p.Asp379His)
c.886G>C (p.Asp296His)
c.794G>C (p.Arg265Pro)
n.1320G>C
c.1144G>C (p.Asp382His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6300930G=CA1435772412WFS1c.1171G= (p.Asp391=)
c.1112G=
c.1135G= (p.Asp379=)
c.886G= (p.Asp296=)
c.794G= (p.Arg265=)
n.1320G=
c.1144G= (p.Asp382=)
4g.6300930G>TCA356174324WFS1c.1171G>T (p.Asp391Tyr)
c.1112G>T
c.1135G>T (p.Asp379Tyr)
c.886G>T (p.Asp296Tyr)
c.794G>T (p.Arg265Leu)
n.1320G>T
c.1144G>T (p.Asp382Tyr)
ClinVar dbSNP
4g.6300931A=CA1435772414WFS1c.1172A= (p.Asp391=)
c.1113A=
c.1136A= (p.Asp379=)
c.887A= (p.Asp296=)
c.795A= (p.Arg265=)
n.1321A=
c.1145A= (p.Asp382=)
4g.6300931A>CCA356174325WFS1c.1172A>C (p.Asp391Ala)
c.1113A>C
c.1136A>C (p.Asp379Ala)
c.887A>C (p.Asp296Ala)
c.795A>C (p.Arg265=)
n.1321A>C
c.1145A>C (p.Asp382Ala)
gnomAD v4
4g.6300931A>GCA356174326WFS1c.1172A>G (p.Asp391Gly)
c.1113A>G
c.1136A>G (p.Asp379Gly)
c.887A>G (p.Asp296Gly)
c.795A>G (p.Arg265=)
n.1321A>G
c.1145A>G (p.Asp382Gly)
4g.6300931A>TCA356174327WFS1c.1172A>T (p.Asp391Val)
c.1113A>T
c.1136A>T (p.Asp379Val)
c.887A>T (p.Asp296Val)
c.795A>T (p.Arg265=)
n.1321A>T
c.1145A>T (p.Asp382Val)
dbSNP gnomAD v2 gnomAD v4
4g.6300932C>ACA356174328WFS1c.1173C>A (p.Asp391Glu)
c.1114C>A
c.1137C>A (p.Asp379Glu)
c.888C>A (p.Asp296Glu)
c.796C>A (p.Pro266Thr)
n.1322C>A
c.1146C>A (p.Asp382Glu)
4g.6300932C=CA1435772415WFS1c.1173C= (p.Asp391=)
c.1114C=
c.1137C= (p.Asp379=)
c.888C= (p.Asp296=)
c.796C= (p.Pro266=)
n.1322C=
c.1146C= (p.Asp382=)
4g.6300932C>GCA2839232WFS1c.1173C>G (p.Asp391Glu)
c.1114C>G
c.1137C>G (p.Asp379Glu)
c.888C>G (p.Asp296Glu)
c.796C>G (p.Pro266Ala)
n.1322C>G
c.1146C>G (p.Asp382Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300932C>TCA438368092WFS1c.1173C>T (p.Asp391=)
c.1114C>T
c.1137C>T (p.Asp379=)
c.888C>T (p.Asp296=)
c.796C>T (p.Pro266Ser)
n.1322C>T
c.1146C>T (p.Asp382=)
gnomAD v4
4g.6300933C>ACA356174329WFS1c.1174C>A (p.Leu392Met)
c.1115C>A
c.1138C>A (p.Leu380Met)
c.889C>A (p.Leu297Met)
c.797C>A (p.Pro266His)
n.1323C>A
c.1147C>A (p.Leu383Met)
4g.6300933C=CA1435772417WFS1c.1174C= (p.Leu392=)
c.1115C=
c.1138C= (p.Leu380=)
c.889C= (p.Leu297=)
c.797C= (p.Pro266=)
n.1323C=
c.1147C= (p.Leu383=)
4g.6300933C>GCA356174330WFS1c.1174C>G (p.Leu392Val)
c.1115C>G
c.1138C>G (p.Leu380Val)
c.889C>G (p.Leu297Val)
c.797C>G (p.Pro266Arg)
n.1323C>G
c.1147C>G (p.Leu383Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6300933C>TCA438368093WFS1c.1174C>T (p.Leu392=)
c.1115C>T
c.1138C>T (p.Leu380=)
c.889C>T (p.Leu297=)
c.797C>T (p.Pro266Leu)
n.1323C>T
c.1147C>T (p.Leu383=)
gnomAD v4
4g.6300934T>ACA356174331WFS1c.1175T>A (p.Leu392Gln)
c.1116T>A
c.1139T>A (p.Leu380Gln)
c.890T>A (p.Leu297Gln)
c.798T>A (p.Pro266=)
n.1324T>A
c.1148T>A (p.Leu383Gln)
4g.6300934T>CCA356174332WFS1c.1175T>C (p.Leu392Pro)
c.1116T>C
c.1139T>C (p.Leu380Pro)
c.890T>C (p.Leu297Pro)
c.798T>C (p.Pro266=)
n.1324T>C
c.1148T>C (p.Leu383Pro)
4g.6300934T>GCA356174333WFS1c.1175T>G (p.Leu392Arg)
c.1116T>G
c.1139T>G (p.Leu380Arg)
c.890T>G (p.Leu297Arg)
c.798T>G (p.Pro266=)
n.1324T>G
c.1148T>G (p.Leu383Arg)
gnomAD v4
4g.6300935G>ACA438368095WFS1c.1176G>A (p.Leu392=)
c.1117G>A
c.1140G>A (p.Leu380=)
c.891G>A (p.Leu297=)
c.799G>A (p.Ala267Thr)
n.1325G>A
c.1149G>A (p.Leu383=)
4g.6300935G>CCA438368096WFS1c.1176G>C (p.Leu392=)
c.1117G>C
c.1140G>C (p.Leu380=)
c.891G>C (p.Leu297=)
c.799G>C (p.Ala267Pro)
n.1325G>C
c.1149G>C (p.Leu383=)
4g.6300935G>TCA438368097WFS1c.1176G>T (p.Leu392=)
c.1117G>T
c.1140G>T (p.Leu380=)
c.891G>T (p.Leu297=)
c.799G>T (p.Ala267Ser)
n.1325G>T
c.1149G>T (p.Leu383=)
4g.6300936C>ACA356174334WFS1c.1177C>A (p.Leu393Met)
c.1118C>A
c.1141C>A (p.Leu381Met)
c.892C>A (p.Leu298Met)
c.800C>A (p.Ala267Asp)
n.1326C>A
c.1150C>A (p.Leu384Met)
4g.6300936C=CA1435772418WFS1c.1177C= (p.Leu393=)
c.1118C=
c.1141C= (p.Leu381=)
c.892C= (p.Leu298=)
c.800C= (p.Ala267=)
n.1326C=
c.1150C= (p.Leu384=)
4g.6300936C>GCA356174335WFS1c.1177C>G (p.Leu393Val)
c.1118C>G
c.1141C>G (p.Leu381Val)
c.892C>G (p.Leu298Val)
c.800C>G (p.Ala267Gly)
n.1326C>G
c.1150C>G (p.Leu384Val)
4g.6300936C>TCA438368098WFS1c.1177C>T (p.Leu393=)
c.1118C>T
c.1141C>T (p.Leu381=)
c.892C>T (p.Leu298=)
c.800C>T (p.Ala267Val)
n.1326C>T
c.1150C>T (p.Leu384=)
dbSNP gnomAD v3 gnomAD v4
4g.6300937T>ACA356174336WFS1c.1178T>A (p.Leu393Gln)
c.1119T>A
c.1142T>A (p.Leu381Gln)
c.893T>A (p.Leu298Gln)
c.801T>A (p.Ala267=)
n.1327T>A
c.1151T>A (p.Leu384Gln)
4g.6300937T>CCA207721WFS1c.1178T>C (p.Leu393Pro)
c.1119T>C
c.1142T>C (p.Leu381Pro)
c.893T>C (p.Leu298Pro)
c.801T>C (p.Ala267=)
n.1327T>C
c.1151T>C (p.Leu384Pro)
ClinVar dbSNP
4g.6300937T>GCA356174337WFS1c.1178T>G (p.Leu393Arg)
c.1119T>G
c.1142T>G (p.Leu381Arg)
c.893T>G (p.Leu298Arg)
c.801T>G (p.Ala267=)
n.1327T>G
c.1151T>G (p.Leu384Arg)
4g.6300937T=CA1435772419WFS1c.1178T= (p.Leu393=)
c.1119T=
c.1142T= (p.Leu381=)
c.893T= (p.Leu298=)
c.801T= (p.Ala267=)
n.1327T=
c.1151T= (p.Leu384=)
4g.6300938G>ACA2839233WFS1c.1179G>A (p.Leu393=)
c.1120G>A
c.1143G>A (p.Leu381=)
c.894G>A (p.Leu298=)
c.802G>A (p.Ala268Thr)
n.1328G>A
c.1152G>A (p.Leu384=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300938G>CCA438368102WFS1c.1179G>C (p.Leu393=)
c.1120G>C
c.1143G>C (p.Leu381=)
c.894G>C (p.Leu298=)
c.802G>C (p.Ala268Pro)
n.1328G>C
c.1152G>C (p.Leu384=)
dbSNP gnomAD v4
4g.6300938G=CA1435772422WFS1c.1179G= (p.Leu393=)
c.1120G=
c.1143G= (p.Leu381=)
c.894G= (p.Leu298=)
c.802G= (p.Ala268=)
n.1328G=
c.1152G= (p.Leu384=)
4g.6300938G>TCA438368103WFS1c.1179G>T (p.Leu393=)
c.1120G>T
c.1143G>T (p.Leu381=)
c.894G>T (p.Leu298=)
c.802G>T (p.Ala268Ser)
n.1328G>T
c.1152G>T (p.Leu384=)
4g.6300939C>ACA356174338WFS1c.1180C>A (p.Leu394Met)
c.1121C>A
c.1144C>A (p.Leu382Met)
c.895C>A (p.Leu299Met)
c.803C>A (p.Ala268Asp)
n.1329C>A
c.1153C>A (p.Leu385Met)
4g.6300939C=CA1435772424WFS1c.1180C= (p.Leu394=)
c.1121C=
c.1144C= (p.Leu382=)
c.895C= (p.Leu299=)
c.803C= (p.Ala268=)
n.1329C=
c.1153C= (p.Leu385=)
4g.6300939C>GCA356174339WFS1c.1180C>G (p.Leu394Val)
c.1121C>G
c.1144C>G (p.Leu382Val)
c.895C>G (p.Leu299Val)
c.803C>G (p.Ala268Gly)
n.1329C>G
c.1153C>G (p.Leu385Val)
4g.6300939C>TCA2839234WFS1c.1180C>T (p.Leu394=)
c.1121C>T
c.1144C>T (p.Leu382=)
c.895C>T (p.Leu299=)
c.803C>T (p.Ala268Val)
n.1329C>T
c.1153C>T (p.Leu385=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300940T>ACA356174341WFS1c.1181T>A (p.Leu394Gln)
c.1122T>A
c.1145T>A (p.Leu382Gln)
c.896T>A (p.Leu299Gln)
c.804T>A (p.Ala268=)
n.1330T>A
c.1154T>A (p.Leu385Gln)
4g.6300940T>CCA91796230WFS1c.1181T>C (p.Leu394Pro)
c.1122T>C
c.1145T>C (p.Leu382Pro)
c.896T>C (p.Leu299Pro)
c.804T>C (p.Ala268=)
n.1330T>C
c.1154T>C (p.Leu385Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6300940T>GCA356174340WFS1c.1181T>G (p.Leu394Arg)
c.1122T>G
c.1145T>G (p.Leu382Arg)
c.896T>G (p.Leu299Arg)
c.804T>G (p.Ala268=)
n.1330T>G
c.1154T>G (p.Leu385Arg)
4g.6300940T=CA1435772426WFS1c.1181T= (p.Leu394=)
c.1122T=
c.1145T= (p.Leu382=)
c.896T= (p.Leu299=)
c.804T= (p.Ala268=)
n.1330T=
c.1154T= (p.Leu385=)
4g.6300941G>ACA438368107WFS1c.1182G>A (p.Leu394=)
c.1123G>A
c.1146G>A (p.Leu382=)
c.897G>A (p.Leu299=)
c.805G>A (p.Ala269Thr)
n.1331G>A
c.1155G>A (p.Leu385=)
dbSNP gnomAD v3 gnomAD v4
4g.6300941G>CCA438368109WFS1c.1182G>C (p.Leu394=)
c.1123G>C
c.1146G>C (p.Leu382=)
c.897G>C (p.Leu299=)
c.805G>C (p.Ala269Pro)
n.1331G>C
c.1155G>C (p.Leu385=)
4g.6300941G>TCA438368110WFS1c.1182G>T (p.Leu394=)
c.1123G>T
c.1146G>T (p.Leu382=)
c.897G>T (p.Leu299=)
c.805G>T (p.Ala269Ser)
n.1331G>T
c.1155G>T (p.Leu385=)
4g.6300942C>ACA356174342WFS1c.1183C>A (p.Arg395Ser)
c.1124C>A
c.1147C>A (p.Arg383Ser)
c.898C>A (p.Arg300Ser)
c.806C>A (p.Ala269Glu)
n.1332C>A
c.1156C>A (p.Arg386Ser)
gnomAD v4
4g.6300942C=CA1435772429WFS1c.1183C= (p.Arg395=)
c.1124C=
c.1147C= (p.Arg383=)
c.898C= (p.Arg300=)
c.806C= (p.Ala269=)
n.1332C=
c.1156C= (p.Arg386=)
4g.6300942C>GCA356174343WFS1c.1183C>G (p.Arg395Gly)
c.1124C>G
c.1147C>G (p.Arg383Gly)
c.898C>G (p.Arg300Gly)
c.806C>G (p.Ala269Gly)
n.1332C>G
c.1156C>G (p.Arg386Gly)
4g.6300942C>TCA2839235WFS1c.1183C>T (p.Arg395Cys)
c.1124C>T
c.1147C>T (p.Arg383Cys)
c.898C>T (p.Arg300Cys)
c.806C>T (p.Ala269Val)
n.1332C>T
c.1156C>T (p.Arg386Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300943G>ACA2839237WFS1c.1184G>A (p.Arg395His)
c.1125G>A
c.1148G>A (p.Arg383His)
c.899G>A (p.Arg300His)
c.807G>A (p.Ala269=)
n.1333G>A
c.1157G>A (p.Arg386His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300943G>CCA2839238WFS1c.1184G>C (p.Arg395Pro)
c.1125G>C
c.1148G>C (p.Arg383Pro)
c.899G>C (p.Arg300Pro)
c.807G>C (p.Ala269=)
n.1333G>C
c.1157G>C (p.Arg386Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300943G=CA1435772433WFS1c.1184G= (p.Arg395=)
c.1125G=
c.1148G= (p.Arg383=)
c.899G= (p.Arg300=)
c.807G= (p.Ala269=)
n.1333G=
c.1157G= (p.Arg386=)
4g.6300943G>TCA2839236WFS1c.1184G>T (p.Arg395Leu)
c.1125G>T
c.1148G>T (p.Arg383Leu)
c.899G>T (p.Arg300Leu)
c.807G>T (p.Ala269=)
n.1333G>T
c.1157G>T (p.Arg386Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.6300944C>ACA438368113WFS1c.1185C>A (p.Arg395=)
c.1126C>A
c.1149C>A (p.Arg383=)
c.900C>A (p.Arg300=)
c.808C>A (p.Leu270Ile)
n.1334C>A
c.1158C>A (p.Arg386=)
4g.6300944C=CA1435772435WFS1c.1185C= (p.Arg395=)
c.1126C=
c.1149C= (p.Arg383=)
c.900C= (p.Arg300=)
c.808C= (p.Leu270=)
n.1334C=
c.1158C= (p.Arg386=)
4g.6300944C>GCA438368114WFS1c.1185C>G (p.Arg395=)
c.1126C>G
c.1149C>G (p.Arg383=)
c.900C>G (p.Arg300=)
c.808C>G (p.Leu270Val)
n.1334C>G
c.1158C>G (p.Arg386=)
4g.6300944C>TCA438368115WFS1c.1185C>T (p.Arg395=)
c.1126C>T
c.1149C>T (p.Arg383=)
c.900C>T (p.Arg300=)
c.808C>T (p.Leu270Phe)
n.1334C>T
c.1158C>T (p.Arg386=)
ClinVar dbSNP gnomAD v4
4g.6300945T>ACA356174344WFS1c.1186T>A (p.Phe396Ile)
c.1127T>A
c.1150T>A (p.Phe384Ile)
c.901T>A (p.Phe301Ile)
c.809T>A (p.Leu270His)
n.1335T>A
c.1159T>A (p.Phe387Ile)
4g.6300945T>CCA356174346WFS1c.1186T>C (p.Phe396Leu)
c.1127T>C
c.1150T>C (p.Phe384Leu)
c.901T>C (p.Phe301Leu)
c.809T>C (p.Leu270Pro)
n.1335T>C
c.1159T>C (p.Phe387Leu)
gnomAD v4
4g.6300945T>GCA356174345WFS1c.1186T>G (p.Phe396Val)
c.1127T>G
c.1150T>G (p.Phe384Val)
c.901T>G (p.Phe301Val)
c.809T>G (p.Leu270Arg)
n.1335T>G
c.1159T>G (p.Phe387Val)
4g.6300946T>ACA356174347WFS1c.1187T>A (p.Phe396Tyr)
c.1128T>A
c.1151T>A (p.Phe384Tyr)
c.902T>A (p.Phe301Tyr)
c.810T>A (p.Leu270=)
n.1336T>A
c.1160T>A (p.Phe387Tyr)
4g.6300946T>CCA356174348WFS1c.1187T>C (p.Phe396Ser)
c.1128T>C
c.1151T>C (p.Phe384Ser)
c.902T>C (p.Phe301Ser)
c.810T>C (p.Leu270=)
n.1336T>C
c.1160T>C (p.Phe387Ser)
4g.6300946T>GCA356174349WFS1c.1187T>G (p.Phe396Cys)
c.1128T>G
c.1151T>G (p.Phe384Cys)
c.902T>G (p.Phe301Cys)
c.810T>G (p.Leu270=)
n.1336T>G
c.1160T>G (p.Phe387Cys)
4g.6300947C>ACA356174350WFS1c.1188C>A (p.Phe396Leu)
c.1129C>A
c.1152C>A (p.Phe384Leu)
c.903C>A (p.Phe301Leu)
c.811C>A (p.Arg271=)
n.1337C>A
c.1161C>A (p.Phe387Leu)
dbSNP gnomAD v3 gnomAD v4
4g.6300947C=CA1435772437WFS1c.1188C= (p.Phe396=)
c.1129C=
c.1152C= (p.Phe384=)
c.903C= (p.Phe301=)
c.811C= (p.Arg271=)
n.1337C=
c.1161C= (p.Phe387=)
4g.6300947C>GCA356174351WFS1c.1188C>G (p.Phe396Leu)
c.1129C>G
c.1152C>G (p.Phe384Leu)
c.903C>G (p.Phe301Leu)
c.811C>G (p.Arg271Gly)
n.1337C>G
c.1161C>G (p.Phe387Leu)
dbSNP gnomAD v4
4g.6300947C>TCA182616WFS1c.1188C>T (p.Phe396=)
c.1129C>T
c.1152C>T (p.Phe384=)
c.903C>T (p.Phe301=)
c.811C>T (p.Arg271Ter)
n.1337C>T
c.1161C>T (p.Phe387=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300948delCA2760284697WFS1c.1189del (p.Glu397SerfsTer?)
c.1130del
c.1153del (p.Glu385SerfsTer?)
c.904del (p.Glu302SerfsTer?)
c.812del (p.Arg271GlnfsTer?)
n.1338del
c.1162del (p.Glu388SerfsTer?)
4g.6300948G>ACA295789WFS1c.1189G>A (p.Glu397Lys)
c.1130G>A
c.1153G>A (p.Glu385Lys)
c.904G>A (p.Glu302Lys)
c.812G>A (p.Arg271Gln)
n.1338G>A
c.1162G>A (p.Glu388Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300948G>CCA356174352WFS1c.1189G>C (p.Glu397Gln)
c.1130G>C
c.1153G>C (p.Glu385Gln)
c.904G>C (p.Glu302Gln)
c.812G>C (p.Arg271Pro)
n.1338G>C
c.1162G>C (p.Glu388Gln)
ClinVar gnomAD v4
4g.6300948G=CA1435772441WFS1c.1189G= (p.Glu397=)
c.1130G=
c.1153G= (p.Glu385=)
c.904G= (p.Glu302=)
c.812G= (p.Arg271=)
n.1338G=
c.1162G= (p.Glu388=)
4g.6300948G>TCA356174353WFS1c.1189G>T (p.Glu397Ter)
c.1130G>T
c.1153G>T (p.Glu385Ter)
c.904G>T (p.Glu302Ter)
c.812G>T (p.Arg271Leu)
n.1338G>T
c.1162G>T (p.Glu388Ter)
dbSNP gnomAD v3 gnomAD v4
4g.6300949A>CCA356174354WFS1c.1190A>C (p.Glu397Ala)
c.1131A>C
c.1154A>C (p.Glu385Ala)
c.905A>C (p.Glu302Ala)
c.813A>C (p.Arg271=)
n.1339A>C
c.1163A>C (p.Glu388Ala)
4g.6300949A>GCA356174355WFS1c.1190A>G (p.Glu397Gly)
c.1131A>G
c.1154A>G (p.Glu385Gly)
c.905A>G (p.Glu302Gly)
c.813A>G (p.Arg271=)
n.1339A>G
c.1163A>G (p.Glu388Gly)
gnomAD v4
4g.6300949A>TCA356174356WFS1c.1190A>T (p.Glu397Val)
c.1131A>T
c.1154A>T (p.Glu385Val)
c.905A>T (p.Glu302Val)
c.813A>T (p.Arg271=)
n.1339A>T
c.1163A>T (p.Glu388Val)
4g.6300950G>ACA438368121WFS1c.1191G>A (p.Glu397=)
c.1132G>A
c.1155G>A (p.Glu385=)
c.906G>A (p.Glu302=)
c.814G>A (p.Ala272Thr)
n.1340G>A
c.1164G>A (p.Glu388=)
4g.6300950G>CCA356174357WFS1c.1191G>C (p.Glu397Asp)
c.1132G>C
c.1155G>C (p.Glu385Asp)
c.906G>C (p.Glu302Asp)
c.814G>C (p.Ala272Pro)
n.1340G>C
c.1164G>C (p.Glu388Asp)
4g.6300950G>TCA356174358WFS1c.1191G>T (p.Glu397Asp)
c.1132G>T
c.1155G>T (p.Glu385Asp)
c.906G>T (p.Glu302Asp)
c.814G>T (p.Ala272Ser)
n.1340G>T
c.1164G>T (p.Glu388Asp)
4g.6300950_6300952delCA2760284702WFS1c.1191_1193del (p.Glu397_Pro398delinsAsp)
c.1132_1134del
c.1155_1157del (p.Glu385_Pro386delinsAsp)
c.906_908del (p.Glu302_Pro303delinsAsp)
c.814_816del (p.Ala272del)
n.1340_1342del
c.1164_1166del (p.Glu388_Pro389delinsAsp)
4g.6300951C>ACA356174359WFS1c.1192C>A (p.Pro398Thr)
c.1133C>A
c.1156C>A (p.Pro386Thr)
c.907C>A (p.Pro303Thr)
c.815C>A (p.Ala272Asp)
n.1341C>A
c.1165C>A (p.Pro389Thr)
4g.6300951C>GCA356174360WFS1c.1192C>G (p.Pro398Ala)
c.1133C>G
c.1156C>G (p.Pro386Ala)
c.907C>G (p.Pro303Ala)
c.815C>G (p.Ala272Gly)
n.1341C>G
c.1165C>G (p.Pro389Ala)
4g.6300951C>TCA356174361WFS1c.1192C>T (p.Pro398Ser)
c.1133C>T
c.1156C>T (p.Pro386Ser)
c.907C>T (p.Pro303Ser)
c.815C>T (p.Ala272Val)
n.1341C>T
c.1165C>T (p.Pro389Ser)
gnomAD v4 COSMIC
4g.6300952C>ACA356174362WFS1c.1193C>A (p.Pro398His)
c.1134C>A
c.1157C>A (p.Pro386His)
c.908C>A (p.Pro303His)
c.816C>A (p.Ala272=)
n.1342C>A
c.1166C>A (p.Pro389His)
dbSNP gnomAD v2 gnomAD v4
4g.6300952C=CA1435772442WFS1c.1193C= (p.Pro398=)
c.1134C=
c.1157C= (p.Pro386=)
c.908C= (p.Pro303=)
c.816C= (p.Ala272=)
n.1342C=
c.1166C= (p.Pro389=)
4g.6300952C>GCA356174363WFS1c.1193C>G (p.Pro398Arg)
c.1134C>G
c.1157C>G (p.Pro386Arg)
c.908C>G (p.Pro303Arg)
c.816C>G (p.Ala272=)
n.1342C>G
c.1166C>G (p.Pro389Arg)
4g.6300952C>TCA356174364WFS1c.1193C>T (p.Pro398Leu)
c.1134C>T
c.1157C>T (p.Pro386Leu)
c.908C>T (p.Pro303Leu)
c.816C>T (p.Ala272=)
n.1342C>T
c.1166C>T (p.Pro389Leu)
COSMIC
4g.6300953C>ACA438368124WFS1c.1194C>A (p.Pro398=)
c.1135C>A
c.1158C>A (p.Pro386=)
c.909C>A (p.Pro303=)
c.817C>A (p.Gln273Lys)
n.1343C>A
c.1167C>A (p.Pro389=)
4g.6300953C=CA1435772444WFS1c.1194C= (p.Pro398=)
c.1135C=
c.1158C= (p.Pro386=)
c.909C= (p.Pro303=)
c.817C= (p.Gln273=)
n.1343C=
c.1167C= (p.Pro389=)
4g.6300953C>GCA438368123WFS1c.1194C>G (p.Pro398=)
c.1135C>G
c.1158C>G (p.Pro386=)
c.909C>G (p.Pro303=)
c.817C>G (p.Gln273Glu)
n.1343C>G
c.1167C>G (p.Pro389=)
ClinVar dbSNP gnomAD v4
4g.6300953C>TCA291628WFS1c.1194C>T (p.Pro398=)
c.1135C>T
c.1158C>T (p.Pro386=)
c.909C>T (p.Pro303=)
c.817C>T (p.Gln273Ter)
n.1343C>T
c.1167C>T (p.Pro389=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300954A=CA1435772446WFS1c.1195A= (p.Asn399=)
c.1136A=
c.1159A= (p.Asn387=)
c.910A= (p.Asn304=)
c.818A= (p.Gln273=)
n.1344A=
c.1168A= (p.Asn390=)
4g.6300954A>CCA356174365WFS1c.1195A>C (p.Asn399His)
c.1136A>C
c.1159A>C (p.Asn387His)
c.910A>C (p.Asn304His)
c.818A>C (p.Gln273Pro)
n.1344A>C
c.1168A>C (p.Asn390His)
4g.6300954A>GCA2839239WFS1c.1195A>G (p.Asn399Asp)
c.1136A>G
c.1159A>G (p.Asn387Asp)
c.910A>G (p.Asn304Asp)
c.818A>G (p.Gln273Arg)
n.1344A>G
c.1168A>G (p.Asn390Asp)
dbSNP ExAC gnomAD v2
4g.6300954A>TCA356174366WFS1c.1195A>T (p.Asn399Tyr)
c.1136A>T
c.1159A>T (p.Asn387Tyr)
c.910A>T (p.Asn304Tyr)
c.818A>T (p.Gln273Leu)
n.1344A>T
c.1168A>T (p.Asn390Tyr)
4g.6300955A>CCA356174368WFS1c.1196A>C (p.Asn399Thr)
c.1137A>C
c.1160A>C (p.Asn387Thr)
c.911A>C (p.Asn304Thr)
c.819A>C (p.Gln273His)
n.1345A>C
c.1169A>C (p.Asn390Thr)
4g.6300955A>GCA356174369WFS1c.1196A>G (p.Asn399Ser)
c.1137A>G
c.1160A>G (p.Asn387Ser)
c.911A>G (p.Asn304Ser)
c.819A>G (p.Gln273=)
n.1345A>G
c.1169A>G (p.Asn390Ser)
gnomAD v4
4g.6300955A>TCA356174367WFS1c.1196A>T (p.Asn399Ile)
c.1137A>T
c.1160A>T (p.Asn387Ile)
c.911A>T (p.Asn304Ile)
c.819A>T (p.Gln273His)
n.1345A>T
c.1169A>T (p.Asn390Ile)
gnomAD v4
4g.6300956C>ACA356174370WFS1c.1197C>A (p.Asn399Lys)
c.1138C>A
c.1161C>A (p.Asn387Lys)
c.912C>A (p.Asn304Lys)
c.820C>A (p.Pro274Thr)
n.1346C>A
c.1170C>A (p.Asn390Lys)
4g.6300956C>GCA356174371WFS1c.1197C>G (p.Asn399Lys)
c.1138C>G
c.1161C>G (p.Asn387Lys)
c.912C>G (p.Asn304Lys)
c.820C>G (p.Pro274Ala)
n.1346C>G
c.1170C>G (p.Asn390Lys)
gnomAD v4
4g.6300956C>TCA438368126WFS1c.1197C>T (p.Asn399=)
c.1138C>T
c.1161C>T (p.Asn387=)
c.912C>T (p.Asn304=)
c.820C>T (p.Pro274Ser)
n.1346C>T
c.1170C>T (p.Asn390=)
4g.6300957C>ACA356174372WFS1c.1198C>A (p.Leu400Met)
c.1139C>A
c.1162C>A (p.Leu388Met)
c.913C>A (p.Leu305Met)
c.821C>A (p.Pro274His)
n.1347C>A
c.1171C>A (p.Leu391Met)
4g.6300957C=CA1435772448WFS1c.1198C= (p.Leu400=)
c.1139C=
c.1162C= (p.Leu388=)
c.913C= (p.Leu305=)
c.821C= (p.Pro274=)
n.1347C=
c.1171C= (p.Leu391=)
4g.6300957C>GCA356174373WFS1c.1198C>G (p.Leu400Val)
c.1139C>G
c.1162C>G (p.Leu388Val)
c.913C>G (p.Leu305Val)
c.821C>G (p.Pro274Arg)
n.1347C>G
c.1171C>G (p.Leu391Val)
ClinVar dbSNP
4g.6300957C>TCA438368127WFS1c.1198C>T (p.Leu400=)
c.1139C>T
c.1162C>T (p.Leu388=)
c.913C>T (p.Leu305=)
c.821C>T (p.Pro274Leu)
n.1347C>T
c.1171C>T (p.Leu391=)
4g.6300958T>ACA356174374WFS1c.1199T>A (p.Leu400Gln)
c.1140T>A
c.1163T>A (p.Leu388Gln)
c.914T>A (p.Leu305Gln)
c.822T>A (p.Pro274=)
n.1348T>A
c.1172T>A (p.Leu391Gln)
4g.6300958T>CCA356174375WFS1c.1199T>C (p.Leu400Pro)
c.1140T>C
c.1163T>C (p.Leu388Pro)
c.914T>C (p.Leu305Pro)
c.822T>C (p.Pro274=)
n.1348T>C
c.1172T>C (p.Leu391Pro)
4g.6300958T>GCA356174376WFS1c.1199T>G (p.Leu400Arg)
c.1140T>G
c.1163T>G (p.Leu388Arg)
c.914T>G (p.Leu305Arg)
c.822T>G (p.Pro274=)
n.1348T>G
c.1172T>G (p.Leu391Arg)
gnomAD v4
4g.6300959G>ACA438368131WFS1c.1200G>A (p.Leu400=)
c.1141G>A
c.1164G>A (p.Leu388=)
c.915G>A (p.Leu305=)
c.823G>A (p.Gly275Arg)
n.1349G>A
c.1173G>A (p.Leu391=)
4g.6300959G>CCA438368132WFS1c.1200G>C (p.Leu400=)
c.1141G>C
c.1164G>C (p.Leu388=)
c.915G>C (p.Leu305=)
c.823G>C (p.Gly275Arg)
n.1349G>C
c.1173G>C (p.Leu391=)
gnomAD v4
4g.6300959G>TCA438368133WFS1c.1200G>T (p.Leu400=)
c.1141G>T
c.1164G>T (p.Leu388=)
c.915G>T (p.Leu305=)
c.823G>T (p.Gly275Ter)
n.1349G>T
c.1173G>T (p.Leu391=)
gnomAD v4
4g.6300960G>ACA356174377WFS1c.1201G>A (p.Asp401Asn)
c.1142G>A
c.1165G>A (p.Asp389Asn)
c.916G>A (p.Asp306Asn)
c.824G>A (p.Gly275Glu)
n.1350G>A
c.1174G>A (p.Asp392Asn)
COSMIC
4g.6300960G>CCA2839240WFS1c.1201G>C (p.Asp401His)
c.1142G>C
c.1165G>C (p.Asp389His)
c.916G>C (p.Asp306His)
c.824G>C (p.Gly275Ala)
n.1350G>C
c.1174G>C (p.Asp392His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300960G=CA1435772450WFS1c.1201G= (p.Asp401=)
c.1142G=
c.1165G= (p.Asp389=)
c.916G= (p.Asp306=)
c.824G= (p.Gly275=)
n.1350G=
c.1174G= (p.Asp392=)
4g.6300960G>TCA356174378WFS1c.1201G>T (p.Asp401Tyr)
c.1142G>T
c.1165G>T (p.Asp389Tyr)
c.916G>T (p.Asp306Tyr)
c.824G>T (p.Gly275Val)
n.1350G>T
c.1174G>T (p.Asp392Tyr)
4g.6300961A=CA1435772451WFS1c.1202A= (p.Asp401=)
c.1143A=
c.1166A= (p.Asp389=)
c.917A= (p.Asp306=)
c.825A= (p.Gly275=)
n.1351A=
c.1175A= (p.Asp392=)
4g.6300961A>CCA2839241WFS1c.1202A>C (p.Asp401Ala)
c.1143A>C
c.1166A>C (p.Asp389Ala)
c.917A>C (p.Asp306Ala)
c.825A>C (p.Gly275=)
n.1351A>C
c.1175A>C (p.Asp392Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300961A>GCA356174379WFS1c.1202A>G (p.Asp401Gly)
c.1143A>G
c.1166A>G (p.Asp389Gly)
c.917A>G (p.Asp306Gly)
c.825A>G (p.Gly275=)
n.1351A>G
c.1175A>G (p.Asp392Gly)
gnomAD v4
4g.6300961A>TCA356174380WFS1c.1202A>T (p.Asp401Val)
c.1143A>T
c.1166A>T (p.Asp389Val)
c.917A>T (p.Asp306Val)
c.825A>T (p.Gly275=)
n.1351A>T
c.1175A>T (p.Asp392Val)
4g.6300962T>ACA356174381WFS1c.1203T>A (p.Asp401Glu)
c.1144T>A
c.1167T>A (p.Asp389Glu)
c.918T>A (p.Asp306Glu)
c.826T>A (p.Cys276Ser)
n.1352T>A
c.1176T>A (p.Asp392Glu)
dbSNP
4g.6300962T>CCA438368135WFS1c.1203T>C (p.Asp401=)
c.1144T>C
c.1167T>C (p.Asp389=)
c.918T>C (p.Asp306=)
c.826T>C (p.Cys276Arg)
n.1352T>C
c.1176T>C (p.Asp392=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6300962T>GCA323617WFS1c.1203T>G (p.Asp401Glu)
c.1144T>G
c.1167T>G (p.Asp389Glu)
c.918T>G (p.Asp306Glu)
c.826T>G (p.Cys276Gly)
n.1352T>G
c.1176T>G (p.Asp392Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300962T=CA1435772454WFS1c.1203T= (p.Asp401=)
c.1144T=
c.1167T= (p.Asp389=)
c.918T= (p.Asp306=)
c.826T= (p.Cys276=)
n.1352T=
c.1176T= (p.Asp392=)
4g.6300963G>ACA356174382WFS1c.1204G>A (p.Val402Met)
c.1145G>A
c.1168G>A (p.Val390Met)
c.919G>A (p.Val307Met)
c.827G>A (p.Cys276Tyr)
n.1353G>A
c.1177G>A (p.Val393Met)
4g.6300963G>CCA356174383WFS1c.1204G>C (p.Val402Leu)
c.1145G>C
c.1168G>C (p.Val390Leu)
c.919G>C (p.Val307Leu)
c.827G>C (p.Cys276Ser)
n.1353G>C
c.1177G>C (p.Val393Leu)
4g.6300963G=CA1435772457WFS1c.1204G= (p.Val402=)
c.1145G=
c.1168G= (p.Val390=)
c.919G= (p.Val307=)
c.827G= (p.Cys276=)
n.1353G=
c.1177G= (p.Val393=)
4g.6300963G>TCA356174384WFS1c.1204G>T (p.Val402Leu)
c.1145G>T
c.1168G>T (p.Val390Leu)
c.919G>T (p.Val307Leu)
c.827G>T (p.Cys276Phe)
n.1353G>T
c.1177G>T (p.Val393Leu)
dbSNP gnomAD v3 gnomAD v4
4g.6300964T>ACA356174385WFS1c.1205T>A (p.Val402Glu)
c.1146T>A
c.1169T>A (p.Val390Glu)
c.920T>A (p.Val307Glu)
c.828T>A (p.Cys276Ter)
n.1354T>A
c.1178T>A (p.Val393Glu)
4g.6300964T>CCA356174386WFS1c.1205T>C (p.Val402Ala)
c.1146T>C
c.1169T>C (p.Val390Ala)
c.920T>C (p.Val307Ala)
c.828T>C (p.Cys276=)
n.1354T>C
c.1178T>C (p.Val393Ala)
gnomAD v4
4g.6300964T>GCA356174387WFS1c.1205T>G (p.Val402Gly)
c.1146T>G
c.1169T>G (p.Val390Gly)
c.920T>G (p.Val307Gly)
c.828T>G (p.Cys276Trp)
n.1354T>G
c.1178T>G (p.Val393Gly)
4g.6300965G>ACA438368137WFS1c.1206G>A (p.Val402=)
c.1147G>A
c.1170G>A (p.Val390=)
c.921G>A (p.Val307=)
c.829G>A (p.Gly277Arg)
n.1355G>A
c.1179G>A (p.Val393=)
ClinVar gnomAD v4
4g.6300965G>CCA438368139WFS1c.1206G>C (p.Val402=)
c.1147G>C
c.1170G>C (p.Val390=)
c.921G>C (p.Val307=)
c.829G>C (p.Gly277Arg)
n.1355G>C
c.1179G>C (p.Val393=)
4g.6300965G>TCA438368138WFS1c.1206G>T (p.Val402=)
c.1147G>T
c.1170G>T (p.Val390=)
c.921G>T (p.Val307=)
c.829G>T (p.Gly277Ter)
n.1355G>T
c.1179G>T (p.Val393=)
4g.6300966delCA2586973609WFS1c.1207del (p.Glu403SerfsTer?)
c.1148del
c.1171del (p.Glu391SerfsTer?)
c.922del (p.Glu308SerfsTer?)
c.830del (p.Gly277GlufsTer?)
n.1356del
c.1180del (p.Glu394SerfsTer?)
4g.6300966G>ACA2839242WFS1c.1207G>A (p.Glu403Lys)
c.1148G>A
c.1171G>A (p.Glu391Lys)
c.922G>A (p.Glu308Lys)
c.830G>A (p.Gly277Glu)
n.1356G>A
c.1180G>A (p.Glu394Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300966G>CCA356174388WFS1c.1207G>C (p.Glu403Gln)
c.1148G>C
c.1171G>C (p.Glu391Gln)
c.922G>C (p.Glu308Gln)
c.830G>C (p.Gly277Ala)
n.1356G>C
c.1180G>C (p.Glu394Gln)
4g.6300966G=CA1435772459WFS1c.1207G= (p.Glu403=)
c.1148G=
c.1171G= (p.Glu391=)
c.922G= (p.Glu308=)
c.830G= (p.Gly277=)
n.1356G=
c.1180G= (p.Glu394=)
4g.6300966G>TCA356174389WFS1c.1207G>T (p.Glu403Ter)
c.1148G>T
c.1171G>T (p.Glu391Ter)
c.922G>T (p.Glu308Ter)
c.830G>T (p.Gly277Val)
n.1356G>T
c.1180G>T (p.Glu394Ter)
4g.6300967A=CA1435772460WFS1c.1208A= (p.Glu403=)
c.1149A=
c.1172A= (p.Glu391=)
c.923A= (p.Glu308=)
c.831A= (p.Gly277=)
n.1357A=
c.1181A= (p.Glu394=)
4g.6300967A>CCA356174390WFS1c.1208A>C (p.Glu403Ala)
c.1149A>C
c.1172A>C (p.Glu391Ala)
c.923A>C (p.Glu308Ala)
c.831A>C (p.Gly277=)
n.1357A>C
c.1181A>C (p.Glu394Ala)
4g.6300967A>GCA2839243WFS1c.1208A>G (p.Glu403Gly)
c.1149A>G
c.1172A>G (p.Glu391Gly)
c.923A>G (p.Glu308Gly)
c.831A>G (p.Gly277=)
n.1357A>G
c.1181A>G (p.Glu394Gly)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
4g.6300967A>TCA356174391WFS1c.1208A>T (p.Glu403Val)
c.1149A>T
c.1172A>T (p.Glu391Val)
c.923A>T (p.Glu308Val)
c.831A>T (p.Gly277=)
n.1357A>T
c.1181A>T (p.Glu394Val)
4g.6300968G>ACA2839244WFS1c.1209G>A (p.Glu403=)
c.1150G>A
c.1173G>A (p.Glu391=)
c.924G>A (p.Glu308=)
c.832G>A (p.Ala278Thr)
n.1358G>A
c.1182G>A (p.Glu394=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300968G>CCA356174393WFS1c.1209G>C (p.Glu403Asp)
c.1150G>C
c.1173G>C (p.Glu391Asp)
c.924G>C (p.Glu308Asp)
c.832G>C (p.Ala278Pro)
n.1358G>C
c.1182G>C (p.Glu394Asp)
4g.6300968G=CA1435772463WFS1c.1209G= (p.Glu403=)
c.1150G=
c.1173G= (p.Glu391=)
c.924G= (p.Glu308=)
c.832G= (p.Ala278=)
n.1358G=
c.1182G= (p.Glu394=)
4g.6300968G>TCA356174392WFS1c.1209G>T (p.Glu403Asp)
c.1150G>T
c.1173G>T (p.Glu391Asp)
c.924G>T (p.Glu308Asp)
c.832G>T (p.Ala278Ser)
n.1358G>T
c.1182G>T (p.Glu394Asp)
gnomAD v4
4g.6300969C>ACA356174394WFS1c.1210C>A (p.Gln404Lys)
c.1151C>A
c.1174C>A (p.Gln392Lys)
c.925C>A (p.Gln309Lys)
c.833C>A (p.Ala278Glu)
n.1359C>A
c.1183C>A (p.Gln395Lys)
4g.6300969C=CA1435772466WFS1c.1210C= (p.Gln404=)
c.1151C=
c.1174C= (p.Gln392=)
c.925C= (p.Gln309=)
c.833C= (p.Ala278=)
n.1359C=
c.1183C= (p.Gln395=)
4g.6300969C>GCA356174395WFS1c.1210C>G (p.Gln404Glu)
c.1151C>G
c.1174C>G (p.Gln392Glu)
c.925C>G (p.Gln309Glu)
c.833C>G (p.Ala278Gly)
n.1359C>G
c.1183C>G (p.Gln395Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6300969C>TCA356174396WFS1c.1210C>T (p.Gln404Ter)
c.1151C>T
c.1174C>T (p.Gln392Ter)
c.925C>T (p.Gln309Ter)
c.833C>T (p.Ala278Val)
n.1359C>T
c.1183C>T (p.Gln395Ter)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6300970A=CA1435772468WFS1c.1211A= (p.Gln404=)
c.1152A=
c.1175A= (p.Gln392=)
c.926A= (p.Gln309=)
c.834A= (p.Ala278=)
n.1360A=
c.1184A= (p.Gln395=)
4g.6300970A>CCA356174397WFS1c.1211A>C (p.Gln404Pro)
c.1152A>C
c.1175A>C (p.Gln392Pro)
c.926A>C (p.Gln309Pro)
c.834A>C (p.Ala278=)
n.1360A>C
c.1184A>C (p.Gln395Pro)
4g.6300970A>GCA356174398WFS1c.1211A>G (p.Gln404Arg)
c.1152A>G
c.1175A>G (p.Gln392Arg)
c.926A>G (p.Gln309Arg)
c.834A>G (p.Ala278=)
n.1360A>G
c.1184A>G (p.Gln395Arg)
4g.6300970A>TCA356174399WFS1c.1211A>T (p.Gln404Leu)
c.1152A>T
c.1175A>T (p.Gln392Leu)
c.926A>T (p.Gln309Leu)
c.834A>T (p.Ala278=)
n.1360A>T
c.1184A>T (p.Gln395Leu)
dbSNP gnomAD v2 COSMIC
4g.6300971G>ACA438368142WFS1c.1212G>A (p.Gln404=)
c.1153G>A
c.1176G>A (p.Gln392=)
c.927G>A (p.Gln309=)
c.835G>A (p.Gly279Ser)
n.1361G>A
c.1185G>A (p.Gln395=)
4g.6300971G>CCA356174400WFS1c.1212G>C (p.Gln404His)
c.1153G>C
c.1176G>C (p.Gln392His)
c.927G>C (p.Gln309His)
c.835G>C (p.Gly279Arg)
n.1361G>C
c.1185G>C (p.Gln395His)
4g.6300971G>TCA356174401WFS1c.1212G>T (p.Gln404His)
c.1153G>T
c.1176G>T (p.Gln392His)
c.927G>T (p.Gln309His)
c.835G>T (p.Gly279Cys)
n.1361G>T
c.1185G>T (p.Gln395His)
4g.6300972G>ACA356174402WFS1c.1213G>A (p.Ala405Thr)
c.1154G>A
c.1177G>A (p.Ala393Thr)
c.928G>A (p.Ala310Thr)
c.836G>A (p.Gly279Asp)
n.1362G>A
c.1186G>A (p.Ala396Thr)
ClinVar dbSNP
4g.6300972G>CCA356174404WFS1c.1213G>C (p.Ala405Pro)
c.1154G>C
c.1177G>C (p.Ala393Pro)
c.928G>C (p.Ala310Pro)
c.836G>C (p.Gly279Ala)
n.1362G>C
c.1186G>C (p.Ala396Pro)
4g.6300972G=CA1435772469WFS1c.1213G= (p.Ala405=)
c.1154G=
c.1177G= (p.Ala393=)
c.928G= (p.Ala310=)
c.836G= (p.Gly279=)
n.1362G=
c.1186G= (p.Ala396=)
4g.6300972G>TCA356174403WFS1c.1213G>T (p.Ala405Ser)
c.1154G>T
c.1177G>T (p.Ala393Ser)
c.928G>T (p.Ala310Ser)
c.836G>T (p.Gly279Val)
n.1362G>T
c.1186G>T (p.Ala396Ser)
4g.6300973C>ACA356174405WFS1c.1214C>A (p.Ala405Asp)
c.1155C>A
c.1178C>A (p.Ala393Asp)
c.929C>A (p.Ala310Asp)
c.837C>A (p.Gly279=)
n.1363C>A
c.1187C>A (p.Ala396Asp)
4g.6300973C=CA1435772471WFS1c.1214C= (p.Ala405=)
c.1155C=
c.1178C= (p.Ala393=)
c.929C= (p.Ala310=)
c.837C= (p.Gly279=)
n.1363C=
c.1187C= (p.Ala396=)
4g.6300973C>GCA356174406WFS1c.1214C>G (p.Ala405Gly)
c.1155C>G
c.1178C>G (p.Ala393Gly)
c.929C>G (p.Ala310Gly)
c.837C>G (p.Gly279=)
n.1363C>G
c.1187C>G (p.Ala396Gly)
dbSNP gnomAD v4
4g.6300973C>TCA356174407WFS1c.1214C>T (p.Ala405Val)
c.1155C>T
c.1178C>T (p.Ala393Val)
c.929C>T (p.Ala310Val)
c.837C>T (p.Gly279=)
n.1363C>T
c.1187C>T (p.Ala396Val)
dbSNP gnomAD v2 gnomAD v4
4g.6300974C>ACA438368147WFS1c.1215C>A (p.Ala405=)
c.1156C>A
c.1179C>A (p.Ala393=)
c.930C>A (p.Ala310=)
c.838C>A (p.Arg280=)
n.1364C>A
c.1188C>A (p.Ala396=)
4g.6300974C=CA1435772472WFS1c.1215C= (p.Ala405=)
c.1156C=
c.1179C= (p.Ala393=)
c.930C= (p.Ala310=)
c.838C= (p.Arg280=)
n.1364C=
c.1188C= (p.Ala396=)
4g.6300974C>GCA438368146WFS1c.1215C>G (p.Ala405=)
c.1156C>G
c.1179C>G (p.Ala393=)
c.930C>G (p.Ala310=)
c.838C>G (p.Arg280Gly)
n.1364C>G
c.1188C>G (p.Ala396=)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6300974C>TCA2839245WFS1c.1215C>T (p.Ala405=)
c.1156C>T
c.1179C>T (p.Ala393=)
c.930C>T (p.Ala310=)
c.838C>T (p.Arg280Ter)
n.1364C>T
c.1188C>T (p.Ala396=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300975G>ACA2839246WFS1c.1216G>A (p.Glu406Lys)
c.1157G>A
c.1180G>A (p.Glu394Lys)
c.931G>A (p.Glu311Lys)
c.839G>A (p.Arg280Gln)
n.1365G>A
c.1189G>A (p.Glu397Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300975G>CCA356174409WFS1c.1216G>C (p.Glu406Gln)
c.1157G>C
c.1180G>C (p.Glu394Gln)
c.931G>C (p.Glu311Gln)
c.839G>C (p.Arg280Pro)
n.1365G>C
c.1189G>C (p.Glu397Gln)
dbSNP gnomAD v2 gnomAD v4
4g.6300975G=CA1435772475WFS1c.1216G= (p.Glu406=)
c.1157G=
c.1180G= (p.Glu394=)
c.931G= (p.Glu311=)
c.839G= (p.Arg280=)
n.1365G=
c.1189G= (p.Glu397=)
4g.6300975G>TCA356174408WFS1c.1216G>T (p.Glu406Ter)
c.1157G>T
c.1180G>T (p.Glu394Ter)
c.931G>T (p.Glu311Ter)
c.839G>T (p.Arg280Leu)
n.1365G>T
c.1189G>T (p.Glu397Ter)
ClinVar dbSNP gnomAD v2
4g.6300976A=CA1435772478WFS1c.1217A= (p.Glu406=)
c.1158A=
c.1181A= (p.Glu394=)
c.932A= (p.Glu311=)
c.840A= (p.Arg280=)
n.1366A=
c.1190A= (p.Glu397=)
4g.6300976A>CCA356174410WFS1c.1217A>C (p.Glu406Ala)
c.1158A>C
c.1181A>C (p.Glu394Ala)
c.932A>C (p.Glu311Ala)
c.840A>C (p.Arg280=)
n.1366A>C
c.1190A>C (p.Glu397Ala)
dbSNP
4g.6300976A>GCA356174411WFS1c.1217A>G (p.Glu406Gly)
c.1158A>G
c.1181A>G (p.Glu394Gly)
c.932A>G (p.Glu311Gly)
c.840A>G (p.Arg280=)
n.1366A>G
c.1190A>G (p.Glu397Gly)
4g.6300976A>TCA2839247WFS1c.1217A>T (p.Glu406Val)
c.1158A>T
c.1181A>T (p.Glu394Val)
c.932A>T (p.Glu311Val)
c.840A>T (p.Arg280=)
n.1366A>T
c.1190A>T (p.Glu397Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300977G>ACA438368149WFS1c.1218G>A (p.Glu406=)
c.1159G>A
c.1182G>A (p.Glu394=)
c.933G>A (p.Glu311=)
c.841G>A (p.Gly281Ser)
n.1367G>A
c.1191G>A (p.Glu397=)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6300977G>CCA356174412WFS1c.1218G>C (p.Glu406Asp)
c.1159G>C
c.1182G>C (p.Glu394Asp)
c.933G>C (p.Glu311Asp)
c.841G>C (p.Gly281Arg)
n.1367G>C
c.1191G>C (p.Glu397Asp)
4g.6300977G=CA1435772480WFS1c.1218G= (p.Glu406=)
c.1159G=
c.1182G= (p.Glu394=)
c.933G= (p.Glu311=)
c.841G= (p.Gly281=)
n.1367G=
c.1191G= (p.Glu397=)
4g.6300977G>TCA2839248WFS1c.1218G>T (p.Glu406Asp)
c.1159G>T
c.1182G>T (p.Glu394Asp)
c.933G>T (p.Glu311Asp)
c.841G>T (p.Gly281Cys)
n.1367G>T
c.1191G>T (p.Glu397Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300978G>ACA91796231WFS1c.1219G>A (p.Val407Ile)
c.1160G>A
c.1183G>A (p.Val395Ile)
c.934G>A (p.Val312Ile)
c.842G>A (p.Gly281Asp)
n.1368G>A
c.1192G>A (p.Val398Ile)
dbSNP
4g.6300978G>CCA356174413WFS1c.1219G>C (p.Val407Leu)
c.1160G>C
c.1183G>C (p.Val395Leu)
c.934G>C (p.Val312Leu)
c.842G>C (p.Gly281Ala)
n.1368G>C
c.1192G>C (p.Val398Leu)
gnomAD v4
4g.6300978G=CA1435772483WFS1c.1219G= (p.Val407=)
c.1160G=
c.1183G= (p.Val395=)
c.934G= (p.Val312=)
c.842G= (p.Gly281=)
n.1368G=
c.1192G= (p.Val398=)
4g.6300978G>TCA356174414WFS1c.1219G>T (p.Val407Phe)
c.1160G>T
c.1183G>T (p.Val395Phe)
c.934G>T (p.Val312Phe)
c.842G>T (p.Gly281Val)
n.1368G>T
c.1192G>T (p.Val398Phe)
4g.6300979T>ACA2839249WFS1c.1220T>A (p.Val407Asp)
c.1161T>A
c.1184T>A (p.Val395Asp)
c.935T>A (p.Val312Asp)
c.843T>A (p.Gly281=)
n.1369T>A
c.1193T>A (p.Val398Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300979T>CCA356174415WFS1c.1220T>C (p.Val407Ala)
c.1161T>C
c.1184T>C (p.Val395Ala)
c.935T>C (p.Val312Ala)
c.843T>C (p.Gly281=)
n.1369T>C
c.1193T>C (p.Val398Ala)
4g.6300979T>GCA356174416WFS1c.1220T>G (p.Val407Gly)
c.1161T>G
c.1184T>G (p.Val395Gly)
c.935T>G (p.Val312Gly)
c.843T>G (p.Gly281=)
n.1369T>G
c.1193T>G (p.Val398Gly)
4g.6300979T=CA1435772486WFS1c.1220T= (p.Val407=)
c.1161T=
c.1184T= (p.Val395=)
c.935T= (p.Val312=)
c.843T= (p.Gly281=)
n.1369T=
c.1193T= (p.Val398=)
4g.6300980C>ACA438368153WFS1c.1221C>A (p.Val407=)
c.1162C>A
c.1185C>A (p.Val395=)
c.936C>A (p.Val312=)
c.844C>A (p.Gln282Lys)
n.1370C>A
c.1194C>A (p.Val398=)
gnomAD v3 gnomAD v4
4g.6300980C=CA1435772490WFS1c.1221C= (p.Val407=)
c.1162C=
c.1185C= (p.Val395=)
c.936C= (p.Val312=)
c.844C= (p.Gln282=)
n.1370C=
c.1194C= (p.Val398=)
4g.6300980C>GCA91796232WFS1c.1221C>G (p.Val407=)
c.1162C>G
c.1185C>G (p.Val395=)
c.936C>G (p.Val312=)
c.844C>G (p.Gln282Glu)
n.1370C>G
c.1194C>G (p.Val398=)
ClinVar dbSNP gnomAD v4
4g.6300980C>TCA136330WFS1c.1221C>T (p.Val407=)
c.1162C>T
c.1185C>T (p.Val395=)
c.936C>T (p.Val312=)
c.844C>T (p.Gln282Ter)
n.1370C>T
c.1194C>T (p.Val398=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300981A>CCA356174417WFS1c.1222A>C (p.Asn408His)
c.1163A>C
c.1186A>C (p.Asn396His)
c.937A>C (p.Asn313His)
c.845A>C (p.Gln282Pro)
n.1371A>C
c.1195A>C (p.Asn399His)
4g.6300981A>GCA356174419WFS1c.1222A>G (p.Asn408Asp)
c.1163A>G
c.1186A>G (p.Asn396Asp)
c.937A>G (p.Asn313Asp)
c.845A>G (p.Gln282Arg)
n.1371A>G
c.1195A>G (p.Asn399Asp)
gnomAD v4
4g.6300981A>TCA356174418WFS1c.1222A>T (p.Asn408Tyr)
c.1163A>T
c.1186A>T (p.Asn396Tyr)
c.937A>T (p.Asn313Tyr)
c.845A>T (p.Gln282Leu)
n.1371A>T
c.1195A>T (p.Asn399Tyr)
4g.6300982A=CA1435772492WFS1c.1223A= (p.Asn408=)
c.1164A=
c.1187A= (p.Asn396=)
c.938A= (p.Asn313=)
c.846A= (p.Gln282=)
n.1372A=
c.1196A= (p.Asn399=)
4g.6300982A>CCA356174420WFS1c.1223A>C (p.Asn408Thr)
c.1164A>C
c.1187A>C (p.Asn396Thr)
c.938A>C (p.Asn313Thr)
c.846A>C (p.Gln282His)
n.1372A>C
c.1196A>C (p.Asn399Thr)
ClinVar
4g.6300982A>GCA2839250WFS1c.1223A>G (p.Asn408Ser)
c.1164A>G
c.1187A>G (p.Asn396Ser)
c.938A>G (p.Asn313Ser)
c.846A>G (p.Gln282=)
n.1372A>G
c.1196A>G (p.Asn399Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6300982A>TCA356174421WFS1c.1223A>T (p.Asn408Ile)
c.1164A>T
c.1187A>T (p.Asn396Ile)
c.938A>T (p.Asn313Ile)
c.846A>T (p.Gln282His)
n.1372A>T
c.1196A>T (p.Asn399Ile)
4g.6300983C>ACA356174422WFS1c.1224C>A (p.Asn408Lys)
c.1165C>A
c.1188C>A (p.Asn396Lys)
c.939C>A (p.Asn313Lys)
c.847C>A (p.Leu283Ile)
n.1373C>A
c.1197C>A (p.Asn399Lys)
4g.6300983C=CA1435772494WFS1c.1224C= (p.Asn408=)
c.1165C=
c.1188C= (p.Asn396=)
c.939C= (p.Asn313=)
c.847C= (p.Leu283=)
n.1373C=
c.1197C= (p.Asn399=)
4g.6300983C>GCA356174423WFS1c.1224C>G (p.Asn408Lys)
c.1165C>G
c.1188C>G (p.Asn396Lys)
c.939C>G (p.Asn313Lys)
c.847C>G (p.Leu283Val)
n.1373C>G
c.1197C>G (p.Asn399Lys)
dbSNP
4g.6300983C>TCA91796233WFS1c.1224C>T (p.Asn408=)
c.1165C>T
c.1188C>T (p.Asn396=)
c.939C>T (p.Asn313=)
c.847C>T (p.Leu283Phe)
n.1373C>T
c.1197C>T (p.Asn399=)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6300984T>ACA356174424WFS1c.1225T>A (p.Phe409Ile)
c.1166T>A
c.1189T>A (p.Phe397Ile)
c.940T>A (p.Phe314Ile)
c.848T>A (p.Leu283His)
n.1374T>A
c.1198T>A (p.Phe400Ile)
4g.6300984T>CCA356174425WFS1c.1225T>C (p.Phe409Leu)
c.1166T>C
c.1189T>C (p.Phe397Leu)
c.940T>C (p.Phe314Leu)
c.848T>C (p.Leu283Pro)
n.1374T>C
c.1198T>C (p.Phe400Leu)
4g.6300984T>GCA356174426WFS1c.1225T>G (p.Phe409Val)
c.1166T>G
c.1189T>G (p.Phe397Val)
c.940T>G (p.Phe314Val)
c.848T>G (p.Leu283Arg)
n.1374T>G
c.1198T>G (p.Phe400Val)

Number of alleles fetched