| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36291990T>C | CA411381860 | MYH9 | c.4403A>G (p.Asp1468Gly) n.4635A>G c.4340A>G (p.Asp1447Gly) | ClinVar dbSNP |
| 22 | g.36291990T>A | CA347309 | MYH9 | c.4403A>T (p.Asp1468Val) n.4635A>T c.4340A>T (p.Asp1447Val) | ClinVar dbSNP |
| 22 | g.36291990T= | CA2403800147 | MYH9 | c.4403A= (p.Asp1468=) n.4635A= c.4340A= (p.Asp1447=) | dbSNP |