| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23422190G>C | CA013459 | MYH7 | c.3235C>G (p.Arg1079Gly) n.3341C>G | ClinVar dbSNP |
| 14 | g.23422190G>T | CA036231 | MYH7 | c.3235C>A (p.Arg1079=) n.3341C>A | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23422190G>A | CA013466 | MYH7 | c.3235C>T (p.Arg1079Trp) n.3341C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |