| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36305985G>T | CA411397435 | MYH9 | c.2167C>A (p.Arg723Ser) n.440C>A n.2399C>A c.2104C>A (p.Arg702Ser) | ClinVar dbSNP |
| 22 | g.36305985G>A | CA257095 | MYH9 | c.2167C>T (p.Arg723Cys) n.440C>T n.2399C>T c.2104C>T (p.Arg702Cys) | ClinVar dbSNP gnomAD v4 COSMIC |
| 22 | g.36305985G= | CA2403806732 | MYH9 | c.2167C= (p.Arg723=) n.440C= n.2399C= c.2104C= (p.Arg702=) | dbSNP |
| 22 | g.36305985G>C | CA411397434 | MYH9 | c.2167C>G (p.Arg723Gly) n.440C>G n.2399C>G c.2104C>G (p.Arg702Gly) | ClinVar dbSNP |