| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36292060C>T | CA123739 | MYH9 | c.4333G>A (p.Asp1445Asn) n.4565G>A c.4270G>A (p.Asp1424Asn) | ClinVar dbSNP |
| 22 | g.36292060C>A | CA343280 | MYH9 | c.4333G>T (p.Asp1445Tyr) n.4565G>T c.4270G>T (p.Asp1424Tyr) | ClinVar dbSNP |
| 22 | g.36292060C>G | CA257091 | MYH9 | c.4333G>C (p.Asp1445His) n.4565G>C c.4270G>C (p.Asp1424His) | ClinVar dbSNP |