| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36288285C>A | CA514352342 | MYH9 | c.4962G>T (p.Arg1654=) n.5194G>T c.4899G>T (p.Arg1633=) | dbSNP |
| 22 | g.36288285C>T | CA134549 | MYH9 | c.4962G>A (p.Arg1654=) n.5194G>A c.4899G>A (p.Arg1633=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.36288285C= | CA2403798179 | MYH9 | c.4962G= (p.Arg1654=) n.5194G= c.4899G= (p.Arg1633=) | dbSNP |