Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.102832665A>C | CA115194 | CYP17A1,WBP1L | c.985T>G (p.Tyr329Asp) c.682T>G (p.Tyr228Asp) c.529T>G (p.Tyr177Asp) c.898T>G (p.Tyr300Asp) n.747T>G c.*1696A>C (n.*1696A>C) | ClinVar dbSNP gnomAD v4 |
10 | g.102832665A>T | CA5669423 | CYP17A1,WBP1L | c.985T>A (p.Tyr329Asn) c.682T>A (p.Tyr228Asn) c.529T>A (p.Tyr177Asn) c.898T>A (p.Tyr300Asn) n.747T>A c.*1696A>T (n.*1696A>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |