Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.27926237C>G | CA10575784 | OCA2 | c.1969G>C (p.Gly657Arg) c.1897G>C (p.Gly633Arg) c.1993G>C (p.Gly665Arg) c.1921G>C (p.Gly641Arg) c.1855G>C (p.Gly619Arg) c.1798G>C (p.Gly600Arg) | ClinVar dbSNP |
15 | g.27926237C= | CA2166365096 | OCA2 | c.1969G= (p.Gly657=) c.1897G= (p.Gly633=) c.1993G= (p.Gly665=) c.1921G= (p.Gly641=) c.1855G= (p.Gly619=) c.1798G= (p.Gly600=) | dbSNP |