| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.110911094C>T | CA010431 | MYL2 | c.484G>A (p.Gly162Arg) c.427G>A (p.Gly143Arg) c.442G>A (p.Gly148Arg) | ClinVar dbSNP gnomAD v4 COSMIC |
| 12 | g.110911094C>A | CA386696715 | MYL2 | c.484G>T (p.Gly162Ter) c.427G>T (p.Gly143Ter) c.442G>T (p.Gly148Ter) | ClinVar dbSNP |
| 12 | g.110911094C= | CA2063066646 | MYL2 | c.484G= (p.Gly162=) c.427G= (p.Gly143=) c.442G= (p.Gly148=) | dbSNP |
| 12 | g.110911094C>G | CA386696716 | MYL2 | c.484G>C (p.Gly162Arg) c.427G>C (p.Gly143Arg) c.442G>C (p.Gly148Arg) | dbSNP |