Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.102832577C>T | CA115185 | CYP17A1,WBP1L | c.1073G>A (p.Arg358Gln) c.770G>A (p.Arg257Gln) c.617G>A (p.Arg206Gln) c.986G>A (p.Arg329Gln) n.835G>A c.*1608C>T (n.*1608C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.102832577C= | CA1932870617 | CYP17A1,WBP1L | c.1073G= (p.Arg358=) c.770G= (p.Arg257=) c.617G= (p.Arg206=) c.986G= (p.Arg329=) n.835G= c.*1608C= (n.*1608C=) | dbSNP |