| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.66851880C>T | CA341754 | PC | c.1892G>A (p.Arg631Gln) n.290-1815G>A c.1826-29G>A (n.1826-29G>A) c.*368G>A (n.*368G>A) n.505G>A c.371G>A (p.Arg124Gln) c.596G>A (p.Arg199Gln) c.527G>A (p.Arg176Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 11 | g.66851880C= | CA1979881629 | PC | c.1892G= (p.Arg631=) n.290-1815G= c.1826-29G= (n.1826-29G=) c.*368G= (n.*368G=) n.505G= c.371G= (p.Arg124=) c.596G= (p.Arg199=) c.527G= (p.Arg176=) | dbSNP |