| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.110915765C>A | CA009851 | MYL2 | c.119G>T (p.Arg40Met) c.62G>T (p.Arg21Met) c.94-1441G>T (n.94-1441G>T) | ClinVar dbSNP |
| 12 | g.110915765C>G | CA243563297 | MYL2 | c.119G>C (p.Arg40Thr) c.62G>C (p.Arg21Thr) c.94-1441G>C (n.94-1441G>C) | ClinVar dbSNP |
| 12 | g.110915765C>T | CA009847 | MYL2 | c.119G>A (p.Arg40Lys) c.62G>A (p.Arg21Lys) c.94-1441G>A (n.94-1441G>A) | ClinVar dbSNP |