| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.37232857C>T | CA118897 | RAC2 | n.227G>A c.169G>A (p.Asp57Asn) c.148G>A (p.Asp50Asn) c.37G>A (p.Asp13Asn) n.299G>A | ClinVar dbSNP |
| 22 | g.37232857C= | CA2404246531 | RAC2 | n.227G= c.169G= (p.Asp57=) c.148G= (p.Asp50=) c.37G= (p.Asp13=) n.299G= | dbSNP |