Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129528800C>T | CA354495494 | RHO | c.67C>T (p.Pro23Ser) | ClinVar dbSNP |
3 | g.129528800C>G | CA256695 | RHO | c.67C>G (p.Pro23Ala) | ClinVar dbSNP |
3 | g.129528800C>A | CA354495488 | RHO | c.67C>A (p.Pro23Thr) | ClinVar dbSNP |
3 | g.129528800C= | CA1401205150 | RHO | c.67C= (p.Pro23=) | dbSNP |