Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.122262118A>CCA354152553CASRc.1083A>C (p.Gln361His)
c.600A>C (p.Gln200His)
c.495A>C (p.Gln165His)
3g.122262118A>GCA435425183CASRc.1083A>G (p.Gln361=)
c.600A>G (p.Gln200=)
c.495A>G (p.Gln165=)
ClinVar gnomAD v4
3g.122262118A>TCA354152554CASRc.1083A>T (p.Gln361His)
c.600A>T (p.Gln200His)
c.495A>T (p.Gln165His)
3g.122262119G>ACA354152555CASRc.1084G>A (p.Glu362Lys)
c.601G>A (p.Glu201Lys)
c.496G>A (p.Glu166Lys)
ClinVar dbSNP gnomAD v4 COSMIC
3g.122262119G>CCA354152557CASRc.1084G>C (p.Glu362Gln)
c.601G>C (p.Glu201Gln)
c.496G>C (p.Glu166Gln)
3g.122262119G>TCA354152556CASRc.1084G>T (p.Glu362Ter)
c.601G>T (p.Glu201Ter)
c.496G>T (p.Glu166Ter)
3g.122262120A>CCA354152558CASRc.1085A>C (p.Glu362Ala)
c.602A>C (p.Glu201Ala)
c.497A>C (p.Glu166Ala)
3g.122262120A>GCA354152559CASRc.1085A>G (p.Glu362Gly)
c.602A>G (p.Glu201Gly)
c.497A>G (p.Glu166Gly)
3g.122262120A>TCA354152560CASRc.1085A>T (p.Glu362Val)
c.602A>T (p.Glu201Val)
c.497A>T (p.Glu166Val)
3g.122262121A>CCA354152561CASRc.1086A>C (p.Glu362Asp)
c.603A>C (p.Glu201Asp)
c.498A>C (p.Glu166Asp)
dbSNP
3g.122262121A>GCA435425189CASRc.1086A>G (p.Glu362=)
c.603A>G (p.Glu201=)
c.498A>G (p.Glu166=)
3g.122262121A>TCA354152562CASRc.1086A>T (p.Glu362Asp)
c.603A>T (p.Glu201Asp)
c.498A>T (p.Glu166Asp)
3g.122262122G>ACA2569588CASRc.1087G>A (p.Gly363Ser)
c.604G>A (p.Gly202Ser)
c.499G>A (p.Gly167Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.122262122G>CCA354152563CASRc.1087G>C (p.Gly363Arg)
c.604G>C (p.Gly202Arg)
c.499G>C (p.Gly167Arg)
3g.122262122G=CA1397873393CASRc.1087G= (p.Gly363=)
c.604G= (p.Gly202=)
c.499G= (p.Gly167=)
3g.122262122G>TCA354152564CASRc.1087G>T (p.Gly363Cys)
c.604G>T (p.Gly202Cys)
c.499G>T (p.Gly167Cys)
COSMIC
3g.122262123G>ACA354152565CASRc.1088G>A (p.Gly363Asp)
c.605G>A (p.Gly202Asp)
c.500G>A (p.Gly167Asp)
ClinVar dbSNP gnomAD v4
3g.122262123G>CCA354152566CASRc.1088G>C (p.Gly363Ala)
c.605G>C (p.Gly202Ala)
c.500G>C (p.Gly167Ala)
3g.122262123G=CA1397873398CASRc.1088G= (p.Gly363=)
c.605G= (p.Gly202=)
c.500G= (p.Gly167=)
3g.122262123G>TCA354152567CASRc.1088G>T (p.Gly363Val)
c.605G>T (p.Gly202Val)
c.500G>T (p.Gly167Val)
3g.122262124T>ACA435425192CASRc.1089T>A (p.Gly363=)
c.606T>A (p.Gly202=)
c.501T>A (p.Gly167=)
3g.122262124T>CCA435425193CASRc.1089T>C (p.Gly363=)
c.606T>C (p.Gly202=)
c.501T>C (p.Gly167=)
3g.122262124T>GCA435425195CASRc.1089T>G (p.Gly363=)
c.606T>G (p.Gly202=)
c.501T>G (p.Gly167=)
3g.122262125G>ACA354152570CASRc.1090G>A (p.Ala364Thr)
c.607G>A (p.Ala203Thr)
c.502G>A (p.Ala168Thr)
dbSNP
3g.122262125G>CCA354152569CASRc.1090G>C (p.Ala364Pro)
c.607G>C (p.Ala203Pro)
c.502G>C (p.Ala168Pro)
3g.122262125G>TCA354152568CASRc.1090G>T (p.Ala364Ser)
c.607G>T (p.Ala203Ser)
c.502G>T (p.Ala168Ser)
3g.122262126C>ACA2569589CASRc.1091C>A (p.Ala364Glu)
c.608C>A (p.Ala203Glu)
c.503C>A (p.Ala168Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.122262126C=CA1397873403CASRc.1091C= (p.Ala364=)
c.608C= (p.Ala203=)
c.503C= (p.Ala168=)
3g.122262126C>GCA354152571CASRc.1091C>G (p.Ala364Gly)
c.608C>G (p.Ala203Gly)
c.503C>G (p.Ala168Gly)
3g.122262126C>TCA354152572CASRc.1091C>T (p.Ala364Val)
c.608C>T (p.Ala203Val)
c.503C>T (p.Ala168Val)
ClinVar
3g.122262127A>CCA435425198CASRc.1092A>C (p.Ala364=)
c.609A>C (p.Ala203=)
c.504A>C (p.Ala168=)
ClinVar dbSNP
3g.122262127A>GCA435425203CASRc.1092A>G (p.Ala364=)
c.609A>G (p.Ala203=)
c.504A>G (p.Ala168=)
3g.122262127A>TCA435425206CASRc.1092A>T (p.Ala364=)
c.609A>T (p.Ala203=)
c.504A>T (p.Ala168=)
3g.122262128A>CCA354152573CASRc.1093A>C (p.Lys365Gln)
c.610A>C (p.Lys204Gln)
c.505A>C (p.Lys169Gln)
3g.122262128A>GCA354152574CASRc.1093A>G (p.Lys365Glu)
c.610A>G (p.Lys204Glu)
c.505A>G (p.Lys169Glu)
3g.122262128A>TCA354152575CASRc.1093A>T (p.Lys365Ter)
c.610A>T (p.Lys204Ter)
c.505A>T (p.Lys169Ter)
3g.122262129A>CCA354152576CASRc.1094A>C (p.Lys365Thr)
c.611A>C (p.Lys204Thr)
c.506A>C (p.Lys169Thr)
3g.122262129A>GCA354152577CASRc.1094A>G (p.Lys365Arg)
c.611A>G (p.Lys204Arg)
c.506A>G (p.Lys169Arg)
3g.122262129A>TCA354152578CASRc.1094A>T (p.Lys365Ile)
c.611A>T (p.Lys204Ile)
c.506A>T (p.Lys169Ile)
3g.122262130A>CCA354152579CASRc.1095A>C (p.Lys365Asn)
c.612A>C (p.Lys204Asn)
c.507A>C (p.Lys169Asn)
3g.122262130A>GCA435425209CASRc.1095A>G (p.Lys365=)
c.612A>G (p.Lys204=)
c.507A>G (p.Lys169=)
gnomAD v4
3g.122262130A>TCA354152580CASRc.1095A>T (p.Lys365Asn)
c.612A>T (p.Lys204Asn)
c.507A>T (p.Lys169Asn)
3g.122262131G>ACA354152583CASRc.1096G>A (p.Gly366Arg)
c.613G>A (p.Gly205Arg)
c.508G>A (p.Gly170Arg)
ClinVar dbSNP COSMIC
3g.122262131G>CCA354152582CASRc.1096G>C (p.Gly366Arg)
c.613G>C (p.Gly205Arg)
c.508G>C (p.Gly170Arg)
3g.122262131G=CA1397873407CASRc.1096G= (p.Gly366=)
c.613G= (p.Gly205=)
c.508G= (p.Gly170=)
3g.122262131G>TCA354152581CASRc.1096G>T (p.Gly366Ter)
c.613G>T (p.Gly205Ter)
c.508G>T (p.Gly170Ter)
3g.122262132G>ACA2569590CASRc.1097G>A (p.Gly366Glu)
c.614G>A (p.Gly205Glu)
c.509G>A (p.Gly170Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.122262132G>CCA354152585CASRc.1097G>C (p.Gly366Ala)
c.614G>C (p.Gly205Ala)
c.509G>C (p.Gly170Ala)
3g.122262132G=CA1397873410CASRc.1097G= (p.Gly366=)
c.614G= (p.Gly205=)
c.509G= (p.Gly170=)
3g.122262132G>TCA354152584CASRc.1097G>T (p.Gly366Val)
c.614G>T (p.Gly205Val)
c.509G>T (p.Gly170Val)
ClinVar

Number of alleles fetched