Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.102837076G>A | CA115183 | CYP17A1 | c.286C>T (p.Arg96Trp) n.339C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
10 | g.102837076G>T | CA471495416 | CYP17A1 | c.286C>A (p.Arg96=) n.339C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
10 | g.102837076G= | CA1932841084 | CYP17A1 | c.286C= (p.Arg96=) n.339C= | dbSNP |