Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.47408490G>T | CA020992 | MSH2 | c.301G>T (p.Glu101Ter) c.103G>T (p.Glu35Ter) n.373G>T n.363G>T | ClinVar dbSNP |
2 | g.47408490G>C | CA346729628 | MSH2 | c.301G>C (p.Glu101Gln) c.103G>C (p.Glu35Gln) n.373G>C n.363G>C | ClinVar dbSNP |
2 | g.47408490G>A | CA346729627 | MSH2 | c.301G>A (p.Glu101Lys) c.103G>A (p.Glu35Lys) n.373G>A n.363G>A | ClinVar dbSNP |