Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.152648842G>A | CA128903 | XRCC2 | c.475C>T (p.Arg159Ter) c.643C>T (p.Arg215Ter) n.665C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.152648842G= | CA1753246897 | XRCC2 | c.475C= (p.Arg159=) c.643C= (p.Arg215=) n.665C= | dbSNP |
7 | g.152648842G>T | CA458895338 | XRCC2 | c.475C>A (p.Arg159=) c.643C>A (p.Arg215=) n.665C>A | dbSNP gnomAD v4 |