Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.102831535A>C | CA377938465 | CYP17A1,WBP1L | c.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 |
10 | g.102831535A>G | CA115193 | CYP17A1,WBP1L | c.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 |
10 | g.102831535A= | CA1932868581 | CYP17A1,WBP1L | c.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 |