Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50625442_50625453delCA913088702ARSAc.1222_1233del (p.Ser408_Thr411del)
c.964_975del (p.Ser322_Thr325del)
c.90_101del
c.1119_1130del (p.Val374_Leu377del)
c.1336_1347del (p.Ser446_Thr449del)
22g.50625442_50625453delinsAGTGGTATCACTCA2410958482ARSAc.1222_1233delinsAGTGATACCACT (p.Ser408=)
c.964_975delinsAGTGATACCACT (p.Ser322=)
c.90_101delinsAGTGATACCACT
c.1119_1130delinsAGTGATACCACT (p.Thr373=)
c.1336_1347delinsAGTGATACCACT (p.Ser446=)
22g.50625443_50625452delinsGTGGTATCACCA2410958484ARSAc.1223_1232delinsGTGATACCAC (p.Ser408=)
c.965_974delinsGTGATACCAC (p.Ser322=)
c.91_100delinsGTGATACCAC
c.1120_1129delinsGTGATACCAC (p.Val374=)
c.1337_1346delinsGTGATACCAC (p.Ser446=)
22g.50625447_50625457delCA658824683ARSAc.1222_1232del (p.Ser408CysfsTer15)
c.964_974del (p.Ser322CysfsTer15)
c.90_100del
c.1119_1129del (p.Val374AlafsTer?)
c.1336_1346del (p.Ser446CysfsTer15)
ClinVar dbSNP
22g.50625446_50625454delCA278488ARSAc.1223_1231del (p.Ser408_Thr410del)
c.965_973del (p.Ser322_Thr324del)
c.91_99del
c.1120_1128del (p.Val374_Pro376del)
c.1337_1345del (p.Ser446_Thr448del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
22g.50625446_50625448delinsGTACA2410958487ARSAc.1227_1229delinsTAC (p.Asp409=)
c.969_971delinsTAC (p.Asp323=)
c.95_97delinsTAC
c.1124_1126delinsTAC (p.Ile375=)
c.1341_1343delinsTAC (p.Asp447=)
22g.50625448_50625449delCA1139667192ARSAc.1227_1228del (p.Thr410HisfsTer16)
c.969_970del (p.Thr324HisfsTer16)
c.95_96del
c.1124_1125del (p.Ile375ThrfsTer?)
c.1341_1342del (p.Thr448HisfsTer16)
ClinVar dbSNP
22g.50625448A>CCA412169475ARSAc.1227T>G (p.Asp409Glu)
c.969T>G (p.Asp323Glu)
c.95T>G
c.1124T>G (p.Ile375Arg)
c.1341T>G (p.Asp447Glu)
22g.50625448A>GCA515391336ARSAc.1227T>C (p.Asp409=)
c.969T>C (p.Asp323=)
c.95T>C
c.1124T>C (p.Ile375Thr)
c.1341T>C (p.Asp447=)
ClinVar gnomAD v4
22g.50625448A>TCA412169478ARSAc.1227T>A (p.Asp409Glu)
c.969T>A (p.Asp323Glu)
c.95T>A
c.1124T>A (p.Ile375Lys)
c.1341T>A (p.Asp447Glu)
22g.50625449T>ACA412169488ARSAc.1226A>T (p.Asp409Val)
c.968A>T (p.Asp323Val)
c.94A>T
c.1123A>T (p.Ile375Leu)
c.1340A>T (p.Asp447Val)
22g.50625449T>CCA412169486ARSAc.1226A>G (p.Asp409Gly)
c.968A>G (p.Asp323Gly)
c.94A>G
c.1123A>G (p.Ile375Val)
c.1340A>G (p.Asp447Gly)
22g.50625449T>GCA412169485ARSAc.1226A>C (p.Asp409Ala)
c.968A>C (p.Asp323Ala)
c.94A>C
c.1123A>C (p.Ile375Leu)
c.1340A>C (p.Asp447Ala)
22g.50625450C>ACA412169494ARSAc.1225G>T (p.Asp409Tyr)
c.967G>T (p.Asp323Tyr)
c.93G>T
c.1122G>T (p.Val374=)
c.1339G>T (p.Asp447Tyr)
22g.50625450C>GCA412169499ARSAc.1225G>C (p.Asp409His)
c.967G>C (p.Asp323His)
c.93G>C
c.1122G>C (p.Val374=)
c.1339G>C (p.Asp447His)
22g.50625450C>TCA412169500ARSAc.1225G>A (p.Asp409Asn)
c.967G>A (p.Asp323Asn)
c.93G>A
c.1122G>A (p.Val374=)
c.1339G>A (p.Asp447Asn)
COSMIC
22g.50625451A>CCA412169503ARSAc.1224T>G (p.Ser408Arg)
c.966T>G (p.Ser322Arg)
c.92T>G
c.1121T>G (p.Val374Gly)
c.1338T>G (p.Ser446Arg)
22g.50625451A>GCA515391350ARSAc.1224T>C (p.Ser408=)
c.966T>C (p.Ser322=)
c.92T>C
c.1121T>C (p.Val374Ala)
c.1338T>C (p.Ser446=)
22g.50625451A>TCA412169505ARSAc.1224T>A (p.Ser408Arg)
c.966T>A (p.Ser322Arg)
c.92T>A
c.1121T>A (p.Val374Glu)
c.1338T>A (p.Ser446Arg)
22g.50625452C>ACA412169508ARSAc.1223G>T (p.Ser408Ile)
c.965G>T (p.Ser322Ile)
c.91G>T
c.1120G>T (p.Val374Leu)
c.1337G>T (p.Ser446Ile)
22g.50625452C=CA2410958488ARSAc.1223G= (p.Ser408=)
c.965G= (p.Ser322=)
c.91G=
c.1120G= (p.Val374=)
c.1337G= (p.Ser446=)
22g.50625452C>GCA412169510ARSAc.1223G>C (p.Ser408Thr)
c.965G>C (p.Ser322Thr)
c.91G>C
c.1120G>C (p.Val374Leu)
c.1337G>C (p.Ser446Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50625452C>TCA10324762ARSAc.1223G>A (p.Ser408Asn)
c.965G>A (p.Ser322Asn)
c.91G>A
c.1120G>A (p.Val374Met)
c.1337G>A (p.Ser446Asn)
ClinVar dbSNP ExAC gnomAD v2
22g.50625453T>ACA412169512ARSAc.1222A>T (p.Ser408Cys)
c.964A>T (p.Ser322Cys)
c.90A>T
c.1119A>T (p.Thr373=)
c.1336A>T (p.Ser446Cys)
22g.50625453T>CCA218992ARSAc.1222A>G (p.Ser408Gly)
c.964A>G (p.Ser322Gly)
c.90A>G
c.1119A>G (p.Thr373=)
c.1336A>G (p.Ser446Gly)
ClinVar dbSNP gnomAD v4
22g.50625453T>GCA412169516ARSAc.1222A>C (p.Ser408Arg)
c.964A>C (p.Ser322Arg)
c.90A>C
c.1119A>C (p.Thr373=)
c.1336A>C (p.Ser446Arg)
22g.50625453T=CA2410958489ARSAc.1222A= (p.Ser408=)
c.964A= (p.Ser322=)
c.90A=
c.1119A= (p.Thr373=)
c.1336A= (p.Ser446=)
22g.50625454G>ACA515391358ARSAc.1221C>T (p.His407=)
c.963C>T (p.His321=)
c.89C>T
c.1118C>T (p.Thr373Ile)
c.1335C>T (p.His445=)
22g.50625454G>CCA412169518ARSAc.1221C>G (p.His407Gln)
c.963C>G (p.His321Gln)
c.89C>G
c.1118C>G (p.Thr373Arg)
c.1335C>G (p.His445Gln)
22g.50625454G>TCA412169519ARSAc.1221C>A (p.His407Gln)
c.963C>A (p.His321Gln)
c.89C>A
c.1118C>A (p.Thr373Lys)
c.1335C>A (p.His445Gln)
22g.50625455T>ACA412169526ARSAc.1220A>T (p.His407Leu)
c.962A>T (p.His321Leu)
c.88A>T
c.1117A>T (p.Thr373Ser)
c.1334A>T (p.His445Leu)
22g.50625455T>CCA412169529ARSAc.1220A>G (p.His407Arg)
c.962A>G (p.His321Arg)
c.88A>G
c.1117A>G (p.Thr373Ala)
c.1334A>G (p.His445Arg)
dbSNP gnomAD v3 gnomAD v4
22g.50625455T>GCA412169524ARSAc.1220A>C (p.His407Pro)
c.962A>C (p.His321Pro)
c.88A>C
c.1117A>C (p.Thr373Pro)
c.1334A>C (p.His445Pro)
22g.50625455T=CA2410958490ARSAc.1220A= (p.His407=)
c.962A= (p.His321=)
c.88A=
c.1117A= (p.Thr373=)
c.1334A= (p.His445=)
22g.50625456G>ACA412169531ARSAc.1219C>T (p.His407Tyr)
c.961C>T (p.His321Tyr)
c.87C>T
c.1116C>T (p.Pro372=)
c.1333C>T (p.His445Tyr)
22g.50625456G>CCA412169532ARSAc.1219C>G (p.His407Asp)
c.961C>G (p.His321Asp)
c.87C>G
c.1116C>G (p.Pro372=)
c.1333C>G (p.His445Asp)
22g.50625456G>TCA412169533ARSAc.1219C>A (p.His407Asn)
c.961C>A (p.His321Asn)
c.87C>A
c.1116C>A (p.Pro372=)
c.1333C>A (p.His445Asn)
22g.50625457G>ACA515391364ARSAc.1218C>T (p.Ala406=)
c.960C>T (p.Ala320=)
c.86C>T
c.1115C>T (p.Pro372Leu)
c.1332C>T (p.Ala444=)
COSMIC
22g.50625457G>CCA515391367ARSAc.1218C>G (p.Ala406=)
c.960C>G (p.Ala320=)
c.86C>G
c.1115C>G (p.Pro372Arg)
c.1332C>G (p.Ala444=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50625457G=CA2410958491ARSAc.1218C= (p.Ala406=)
c.960C= (p.Ala320=)
c.86C=
c.1115C= (p.Pro372=)
c.1332C= (p.Ala444=)
22g.50625457G>TCA515391369ARSAc.1218C>A (p.Ala406=)
c.960C>A (p.Ala320=)
c.86C>A
c.1115C>A (p.Pro372His)
c.1332C>A (p.Ala444=)
22g.50625458G>ACA412169536ARSAc.1217C>T (p.Ala406Val)
c.959C>T (p.Ala320Val)
c.85C>T
c.1114C>T (p.Pro372Ser)
c.1331C>T (p.Ala444Val)
22g.50625458G>CCA412169538ARSAc.1217C>G (p.Ala406Gly)
c.959C>G (p.Ala320Gly)
c.85C>G
c.1114C>G (p.Pro372Ala)
c.1331C>G (p.Ala444Gly)
22g.50625458G>TCA412169542ARSAc.1217C>A (p.Ala406Asp)
c.959C>A (p.Ala320Asp)
c.85C>A
c.1114C>A (p.Pro372Thr)
c.1331C>A (p.Ala444Asp)
22g.50625459C>ACA10324763ARSAc.1216G>T (p.Ala406Ser)
c.958G>T (p.Ala320Ser)
c.84G>T
c.1113G>T (p.Leu371=)
c.1330G>T (p.Ala444Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.50625459C=CA2410958492ARSAc.1216G= (p.Ala406=)
c.958G= (p.Ala320=)
c.84G=
c.1113G= (p.Leu371=)
c.1330G= (p.Ala444=)
22g.50625459C>GCA412169550ARSAc.1216G>C (p.Ala406Pro)
c.958G>C (p.Ala320Pro)
c.84G>C
c.1113G>C (p.Leu371=)
c.1330G>C (p.Ala444Pro)
22g.50625459C>TCA412169551ARSAc.1216G>A (p.Ala406Thr)
c.958G>A (p.Ala320Thr)
c.84G>A
c.1113G>A (p.Leu371=)
c.1330G>A (p.Ala444Thr)
gnomAD v4
22g.50625460A>CCA515391383ARSAc.1215T>G (p.Ser405=)
c.957T>G (p.Ser319=)
c.83T>G
c.1112T>G (p.Leu371Arg)
c.1329T>G (p.Ser443=)
22g.50625460A>GCA515391384ARSAc.1215T>C (p.Ser405=)
c.957T>C (p.Ser319=)
c.83T>C
c.1112T>C (p.Leu371Pro)
c.1329T>C (p.Ser443=)

Number of alleles fetched