Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.6301180A>G | CA215002 | WFS1 | c.1421A>G (p.Glu474Gly) c.1362A>G c.1385A>G (p.Glu462Gly) c.1136A>G (p.Glu379Gly) c.1044A>G (p.Arg348=) n.1570A>G c.1394A>G (p.Glu465Gly) | ClinVar dbSNP |
4 | g.6301180A>C | CA356174795 | WFS1 | c.1421A>C (p.Glu474Ala) c.1362A>C c.1385A>C (p.Glu462Ala) c.1136A>C (p.Glu379Ala) c.1044A>C (p.Arg348=) n.1570A>C c.1394A>C (p.Glu465Ala) | ClinVar dbSNP |