| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.49612506C>T | CA122828 | RHAG | c.836G>A (p.Gly279Glu) n.526G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 6 | g.49612506C>G | CA364398545 | RHAG | c.836G>C (p.Gly279Ala) n.526G>C | dbSNP |
| 6 | g.49612506C= | CA1627469194 | RHAG | c.836G= (p.Gly279=) n.526G= | dbSNP |