Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129532722A>G | CA256677 | RHO | c.886A>G (p.Lys296Glu) | ClinVar dbSNP |
3 | g.129532722A>C | CA354470787 | RHO | c.886A>C (p.Lys296Gln) | ClinVar dbSNP |
3 | g.129532722A= | CA1401211987 | RHO | c.886A= (p.Lys296=) | dbSNP |