Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129529002G>A | CA122823 | RHO | c.269G>A (p.Gly90Asp) | ClinVar dbSNP |
3 | g.129529002G>T | CA354496638 | RHO | c.269G>T (p.Gly90Val) | dbSNP gnomAD v4 |
3 | g.129529002G= | CA1401205916 | RHO | c.269G= (p.Gly90=) | dbSNP |