| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.15738685G>A | CA16620076 | MYH11 | c.3001C>T (p.Arg1001Ter) c.3022C>T (p.Arg1008Ter) c.*1184C>T (n.*1184C>T) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 16 | g.15738685G>T | CA493784071 | MYH11 | c.3001C>A (p.Arg1001=) c.3022C>A (p.Arg1008=) c.*1184C>A (n.*1184C>A) | ClinVar dbSNP |