Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.47408483T>G | CA346729614 | MSH2 | c.294T>G (p.Tyr98Ter) c.96T>G (p.Tyr32Ter) n.366T>G n.356T>G | ClinVar dbSNP gnomAD v4 |
2 | g.47408483T>C | CA037726 | MSH2 | c.294T>C (p.Tyr98=) c.96T>C (p.Tyr32=) n.366T>C n.356T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.47408483T>A | CA10584204 | MSH2 | c.294T>A (p.Tyr98Ter) c.96T>A (p.Tyr32Ter) n.366T>A n.356T>A | ClinVar dbSNP |