Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.112775676G>C | CA16022349 | APC | c.470G>C (p.Trp157Ser) n.526G>C c.*476G>C (n.*476G>C) c.500G>C (p.Trp167Ser) c.395G>C (p.Trp132Ser) c.293G>C (p.Trp98Ser) c.-566G>C (n.-566G>C) | dbSNP |
5 | g.112775676G>A | CA009701 | APC | c.470G>A (p.Trp157Ter) n.526G>A c.*476G>A (n.*476G>A) c.500G>A (p.Trp167Ter) c.395G>A (p.Trp132Ter) c.293G>A (p.Trp98Ter) c.-566G>A (n.-566G>A) | ClinVar dbSNP |