Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.102831535A>CCA377938465CYP17A1,WBP1Lc.1216T>G (p.Trp406Gly)
c.913T>G (p.Trp305Gly)
c.760T>G (p.Trp254Gly)
c.1129T>G (p.Trp377Gly)
c.1219T>G (p.Trp407Gly)
n.978T>G
c.*629-63A>C (n.*629-63A>C)
n.169T>G
ClinVar dbSNP
10g.102831535A>GCA115193CYP17A1,WBP1Lc.1216T>C (p.Trp406Arg)
c.913T>C (p.Trp305Arg)
c.760T>C (p.Trp254Arg)
c.1129T>C (p.Trp377Arg)
c.1219T>C (p.Trp407Arg)
n.978T>C
c.*629-63A>G (n.*629-63A>G)
n.169T>C
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.102831535A=CA1932868581CYP17A1,WBP1Lc.1216T= (p.Trp406=)
c.913T= (p.Trp305=)
c.760T= (p.Trp254=)
c.1129T= (p.Trp377=)
c.1219T= (p.Trp407=)
n.978T=
c.*629-63A= (n.*629-63A=)
n.169T=
dbSNP

Number of alleles fetched