Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.46859495C>T | CA013861 | MYL3 | c.461G>A (p.Arg154His) n.683G>A n.419G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.46859495C>A | CA044228 | MYL3 | c.461G>T (p.Arg154Leu) n.683G>T n.419G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.46859495C= | CA1362297082 | MYL3 | c.461G= (p.Arg154=) n.683G= n.419G= | dbSNP |
3 | g.46859495C>G | CA352495900 | MYL3 | c.461G>C (p.Arg154Pro) n.683G>C n.419G>C | dbSNP |