Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.46859490C>T | CA013880 | MYL3 | c.466G>A (p.Val156Met) n.688G>A n.424G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.46859490C>A | CA013890 | MYL3 | c.466G>T (p.Val156Leu) n.688G>T n.424G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.46859490C>G | CA352495892 | MYL3 | c.466G>C (p.Val156Leu) n.688G>C n.424G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |