Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.112801383G>C | CA16023152 | APC | c.834G>C (p.Gln278His) n.890G>C c.*840G>C (n.*840G>C) c.780G>C (p.Gln260His) c.864G>C (p.Gln288His) c.759G>C (p.Gln253His) c.750G>C (p.Gln250His) c.657G>C (p.Gln219His) c.-202G>C (n.-202G>C) | dbSNP COSMIC |
5 | g.112801383G>A | CA16611754 | APC | c.834G>A (p.Gln278=) n.890G>A c.*840G>A (n.*840G>A) c.780G>A (p.Gln260=) c.864G>A (p.Gln288=) c.759G>A (p.Gln253=) c.750G>A (p.Gln250=) c.657G>A (p.Gln219=) c.-202G>A (n.-202G>A) | ClinVar dbSNP |