| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23418343G>C | CA10577505 | MYH7 | c.4036C>G (p.Gln1346Glu) | ClinVar dbSNP COSMIC |
| 14 | g.23418343G>T | CA014382 | MYH7 | c.4036C>A (p.Gln1346Lys) | ClinVar dbSNP |
| 14 | g.23418343G>A | CA389041153 | MYH7 | c.4036C>T (p.Gln1346Ter) | ClinVar dbSNP |
| 14 | g.23418343G= | CA2123442809 | MYH7 | c.4036C= (p.Gln1346=) | dbSNP |