Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129532711C>A | CA122822 | RHO | c.875C>A (p.Ala292Glu) | ClinVar dbSNP |
3 | g.129532711C>T | CA354470722 | RHO | c.875C>T (p.Ala292Val) | ClinVar dbSNP |
3 | g.129532711C= | CA1401211971 | RHO | c.875C= (p.Ala292=) | dbSNP |