Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.74339597C>ACA393146960CYP11A1c.1147G>T (p.Glu383Ter)
c.673G>T (p.Glu225Ter)
15g.74339597C>GCA393146961CYP11A1c.1147G>C (p.Glu383Gln)
c.673G>C (p.Glu225Gln)
15g.74339597C>TCA393146962CYP11A1c.1147G>A (p.Glu383Lys)
c.673G>A (p.Glu225Lys)
COSMIC
15g.74339598C>ACA393146963CYP11A1c.1146G>T (p.Lys382Asn)
c.672G>T (p.Lys224Asn)
dbSNP gnomAD v4 COSMIC
15g.74339598C=CA2187637884CYP11A1c.1146G= (p.Lys382=)
c.672G= (p.Lys224=)
15g.74339598C>GCA393146964CYP11A1c.1146G>C (p.Lys382Asn)
c.672G>C (p.Lys224Asn)
15g.74339598C>TCA7656363CYP11A1c.1146G>A (p.Lys382=)
c.672G>A (p.Lys224=)
dbSNP ExAC gnomAD v4
15g.74339599T>ACA393146967CYP11A1c.1145A>T (p.Lys382Met)
c.671A>T (p.Lys224Met)
15g.74339599T>CCA393146966CYP11A1c.1145A>G (p.Lys382Arg)
c.671A>G (p.Lys224Arg)
15g.74339599T>GCA393146965CYP11A1c.1145A>C (p.Lys382Thr)
c.671A>C (p.Lys224Thr)
15g.74339600delCA2731160687CYP11A1c.1145del (p.Lys382ArgfsTer4)
c.671del (p.Lys224ArgfsTer4)
dbSNP
15g.74339600T>ACA393146968CYP11A1c.1144A>T (p.Lys382Ter)
c.670A>T (p.Lys224Ter)
15g.74339600T>CCA393146970CYP11A1c.1144A>G (p.Lys382Glu)
c.670A>G (p.Lys224Glu)
15g.74339600T>GCA393146969CYP11A1c.1144A>C (p.Lys382Gln)
c.670A>C (p.Lys224Gln)
15g.74339602_74339604dupCA2629468486CYP11A1c.1142_1144dup (p.Ile381_Lys382insIle)
c.668_670dup (p.Ile223_Lys224insIle)
gnomAD v4
15g.74339601G>ACA491194243CYP11A1c.1143C>T (p.Ile381=)
c.669C>T (p.Ile223=)
15g.74339601G>CCA393146971CYP11A1c.1143C>G (p.Ile381Met)
c.669C>G (p.Ile223Met)
gnomAD v4
15g.74339601G>TCA491194245CYP11A1c.1143C>A (p.Ile381=)
c.669C>A (p.Ile223=)
gnomAD v4
15g.74339602A>CCA393146972CYP11A1c.1142T>G (p.Ile381Ser)
c.668T>G (p.Ile223Ser)
15g.74339602A>GCA393146973CYP11A1c.1142T>C (p.Ile381Thr)
c.668T>C (p.Ile223Thr)
15g.74339602A>TCA393146974CYP11A1c.1142T>A (p.Ile381Asn)
c.668T>A (p.Ile223Asn)
15g.74339603T>ACA393146975CYP11A1c.1141A>T (p.Ile381Phe)
c.667A>T (p.Ile223Phe)
15g.74339603T>CCA393146976CYP11A1c.1141A>G (p.Ile381Val)
c.667A>G (p.Ile223Val)
15g.74339603T>GCA393146977CYP11A1c.1141A>C (p.Ile381Leu)
c.667A>C (p.Ile223Leu)
15g.74339604G>ACA491194251CYP11A1c.1140C>T (p.Ser380=)
c.666C>T (p.Ser222=)
15g.74339604G>CCA393146978CYP11A1c.1140C>G (p.Ser380Arg)
c.666C>G (p.Ser222Arg)
15g.74339604G>TCA393146979CYP11A1c.1140C>A (p.Ser380Arg)
c.666C>A (p.Ser222Arg)
15g.74339605C>ACA393146980CYP11A1c.1139G>T (p.Ser380Ile)
c.665G>T (p.Ser222Ile)
15g.74339605C>GCA393146981CYP11A1c.1139G>C (p.Ser380Thr)
c.665G>C (p.Ser222Thr)
15g.74339605C>TCA393146982CYP11A1c.1139G>A (p.Ser380Asn)
c.665G>A (p.Ser222Asn)
15g.74339606T>ACA393146985CYP11A1c.1138A>T (p.Ser380Cys)
c.664A>T (p.Ser222Cys)
15g.74339606T>CCA393146983CYP11A1c.1138A>G (p.Ser380Gly)
c.664A>G (p.Ser222Gly)
15g.74339606T>GCA393146984CYP11A1c.1138A>C (p.Ser380Arg)
c.664A>C (p.Ser222Arg)
15g.74339607G>ACA491194258CYP11A1c.1137C>T (p.Ala379=)
c.663C>T (p.Ala221=)
15g.74339607G>CCA491194260CYP11A1c.1137C>G (p.Ala379=)
c.663C>G (p.Ala221=)
15g.74339607G>TCA491194261CYP11A1c.1137C>A (p.Ala379=)
c.663C>A (p.Ala221=)
15g.74339608G>ACA393146986CYP11A1c.1136C>T (p.Ala379Val)
c.662C>T (p.Ala221Val)
dbSNP gnomAD v3 gnomAD v4
15g.74339608G>CCA393146987CYP11A1c.1136C>G (p.Ala379Gly)
c.662C>G (p.Ala221Gly)
15g.74339608G=CA2187637886CYP11A1c.1136C= (p.Ala379=)
c.662C= (p.Ala221=)
15g.74339608G>TCA393146988CYP11A1c.1136C>A (p.Ala379Asp)
c.662C>A (p.Ala221Asp)
15g.74339609C>ACA393146989CYP11A1c.1135G>T (p.Ala379Ser)
c.661G>T (p.Ala221Ser)
15g.74339609C=CA2187637888CYP11A1c.1135G= (p.Ala379=)
c.661G= (p.Ala221=)
15g.74339609C>GCA393146990CYP11A1c.1135G>C (p.Ala379Pro)
c.661G>C (p.Ala221Pro)
15g.74339609C>TCA7656364CYP11A1c.1135G>A (p.Ala379Thr)
c.661G>A (p.Ala221Thr)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
15g.74339610T>ACA393146991CYP11A1c.1134A>T (p.Lys378Asn)
c.660A>T (p.Lys220Asn)
15g.74339610T>CCA491194267CYP11A1c.1134A>G (p.Lys378=)
c.660A>G (p.Lys220=)
15g.74339610T>GCA393146992CYP11A1c.1134A>C (p.Lys378Asn)
c.660A>C (p.Lys220Asn)
15g.74339611T>ACA393146993CYP11A1c.1133A>T (p.Lys378Ile)
c.659A>T (p.Lys220Ile)
15g.74339611T>CCA272786875CYP11A1c.1133A>G (p.Lys378Arg)
c.659A>G (p.Lys220Arg)
dbSNP gnomAD v4
15g.74339611T>GCA393146994CYP11A1c.1133A>C (p.Lys378Thr)
c.659A>C (p.Lys220Thr)

Number of alleles fetched