| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36289096C>T | CA411379606 | MYH9 | c.4609G>A (p.Val1537Met) n.4841G>A c.4546G>A (p.Val1516Met) | ClinVar dbSNP gnomAD v4 |
| 22 | g.36289096C>A | CA273196 | MYH9 | c.4609G>T (p.Val1537Leu) n.4841G>T c.4546G>T (p.Val1516Leu) | ClinVar dbSNP |
| 22 | g.36289096C= | CA2403798552 | MYH9 | c.4609G= (p.Val1537=) n.4841G= c.4546G= (p.Val1516=) | dbSNP |