Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.16148725C>A | CA338642093 | EPHA2 | c.476G>T (p.Arg159Leu) n.528G>T c.314G>T (p.Arg105Leu) | dbSNP |
1 | g.16148725C>T | CA625513 | EPHA2 | c.476G>A (p.Arg159His) n.528G>A c.314G>A (p.Arg105His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.16148725C= | CA1141365760 | EPHA2 | c.476G= (p.Arg159=) n.528G= c.314G= (p.Arg105=) | dbSNP |