Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.208128343C>A | CA210591 | CRYGC | c.385G>T (p.Gly129Cys) n.98-8713C>A c.256G>T (p.Gly86Cys) | ClinVar dbSNP |
2 | g.208128343C>T | CA350093971 | CRYGC | c.385G>A (p.Gly129Ser) n.98-8713C>T c.256G>A (p.Gly86Ser) | dbSNP |
2 | g.208128343C= | CA1323930893 | CRYGC | c.385G= (p.Gly129=) n.98-8713C= c.256G= (p.Gly86=) | dbSNP |