Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.47410337G>A | CA021573 | MSH2 | c.610G>A (p.Gly204Arg) c.412G>A (p.Gly138Arg) n.682G>A n.672G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.47410337G>C | CA346731092 | MSH2 | c.610G>C (p.Gly204Arg) c.412G>C (p.Gly138Arg) n.682G>C n.672G>C | ClinVar dbSNP |
2 | g.47410337G>T | CA021582 | MSH2 | c.610G>T (p.Gly204Ter) c.412G>T (p.Gly138Ter) n.682G>T n.672G>T | ClinVar dbSNP |