Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.102831589T>C | CA377938589 | CYP17A1,WBP1L | c.1162A>G (p.Lys388Glu) c.859A>G (p.Lys287Glu) c.706A>G (p.Lys236Glu) c.1075A>G (p.Lys359Glu) c.1165A>G (p.Lys389Glu) n.924A>G c.*629-9T>C (n.*629-9T>C) n.115A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.102831589T>A | CA16616913 | CYP17A1,WBP1L | c.1162A>T (p.Lys388Ter) c.859A>T (p.Lys287Ter) c.706A>T (p.Lys236Ter) c.1075A>T (p.Lys359Ter) c.1165A>T (p.Lys389Ter) n.924A>T c.*629-9T>A (n.*629-9T>A) n.115A>T | ClinVar dbSNP gnomAD v4 |
10 | g.102831589T= | CA1932868704 | CYP17A1,WBP1L | c.1162A= (p.Lys388=) c.859A= (p.Lys287=) c.706A= (p.Lys236=) c.1075A= (p.Lys359=) c.1165A= (p.Lys389=) n.924A= c.*629-9T= (n.*629-9T=) n.115A= | dbSNP |