| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23420993C>T | CA013562 | MYH7 | c.3301G>A (p.Gly1101Ser) n.3409G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23420993C>G | CA389044408 | MYH7 | c.3301G>C (p.Gly1101Arg) n.3409G>C | dbSNP gnomAD v4 |
| 14 | g.23420993C= | CA2123448691 | MYH7 | c.3301G= (p.Gly1101=) n.3409G= | dbSNP |