| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.36348958G>A | CA10210691 | MYH9 | n.493C>T n.502C>T c.279C>T (p.Asn93=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.36348958G>C | CA257089 | MYH9 | n.493C>G n.502C>G c.279C>G (p.Asn93Lys) | ClinVar dbSNP |
| 22 | g.36348958G= | CA2403826638 | MYH9 | n.493C= n.502C= c.279C= (p.Asn93=) | dbSNP |