| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36295068C>A | CA343278 | MYH9 | c.3557G>T (p.Arg1186Leu) n.3789G>T c.3494G>T (p.Arg1165Leu) | ClinVar dbSNP |
| 22 | g.36295068C= | CA2403801542 | MYH9 | c.3557G= (p.Arg1186=) n.3789G= c.3494G= (p.Arg1165=) | dbSNP |
| 22 | g.36295068C>G | CA411387917 | MYH9 | c.3557G>C (p.Arg1186Pro) n.3789G>C c.3494G>C (p.Arg1165Pro) | dbSNP gnomAD v4 |
| 22 | g.36295068C>T | CA411387918 | MYH9 | c.3557G>A (p.Arg1186His) n.3789G>A c.3494G>A (p.Arg1165His) | dbSNP gnomAD v4 |