Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.132618182C>T | CA117821 | RAD50 | c.3277C>T (p.Arg1093Ter) c.2980C>T (p.Arg994Ter) n.2885C>T n.3796C>T c.113C>T c.*2903C>T (n.*2903C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
5 | g.132618182C>G | CA360964657 | RAD50 | c.3277C>G (p.Arg1093Gly) c.2980C>G (p.Arg994Gly) n.2885C>G n.3796C>G c.113C>G c.*2903C>G (n.*2903C>G) | ClinVar dbSNP gnomAD v4 |