Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.83204915G>T | CA3332243 | XRCC4 | c.739G>T (p.Ala247Ser) n.751G>T n.808G>T c.79G>T (p.Ala27Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.83204915G>C | CA360359329 | XRCC4 | c.739G>C (p.Ala247Pro) n.751G>C n.808G>C c.79G>C (p.Ala27Pro) | dbSNP |
5 | g.83204915G= | CA1559631323 | XRCC4 | c.739G= (p.Ala247=) n.751G= n.808G= c.79G= (p.Ala27=) | dbSNP |
5 | g.83204915G>A | CA360359330 | XRCC4 | c.739G>A (p.Ala247Thr) n.751G>A n.808G>A c.79G>A (p.Ala27Thr) | dbSNP gnomAD v4 |