Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.102832611G>T | CA377938856 | CYP17A1,WBP1L | c.1039C>A (p.Arg347Ser) c.736C>A (p.Arg246Ser) c.583C>A (p.Arg195Ser) c.952C>A (p.Arg318Ser) n.801C>A c.*1642G>T (n.*1642G>T) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
10 | g.102832611G>A | CA115191 | CYP17A1,WBP1L | c.1039C>T (p.Arg347Cys) c.736C>T (p.Arg246Cys) c.583C>T (p.Arg195Cys) c.952C>T (p.Arg318Cys) n.801C>T c.*1642G>A (n.*1642G>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
10 | g.102832611G>C | CA377938855 | CYP17A1,WBP1L | c.1039C>G (p.Arg347Gly) c.736C>G (p.Arg246Gly) c.583C>G (p.Arg195Gly) c.952C>G (p.Arg318Gly) n.801C>G c.*1642G>C (n.*1642G>C) | ClinVar dbSNP |
10 | g.102832611G= | CA1932870666 | CYP17A1,WBP1L | c.1039C= (p.Arg347=) c.736C= (p.Arg246=) c.583C= (p.Arg195=) c.952C= (p.Arg318=) n.801C= c.*1642G= (n.*1642G=) | dbSNP |