| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.152648822T>A | CA458895316 | XRCC2 | c.495A>T (p.Ile165=) c.663A>T (p.Ile221=) n.685A>T | |
| 7 | g.152648822T>C | CA370198222 | XRCC2 | c.495A>G (p.Ile165Met) c.663A>G (p.Ile221Met) n.685A>G | gnomAD v4 |
| 7 | g.152648822T>G | CA458895317 | XRCC2 | c.495A>C (p.Ile165=) c.663A>C (p.Ile221=) n.685A>C | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648822T= | CA1753246832 | XRCC2 | c.495A= (p.Ile165=) c.663A= (p.Ile221=) n.685A= | |
| 7 | g.152648823A= | CA1753246837 | XRCC2 | c.494T= (p.Ile165=) c.662T= (p.Ile221=) n.684T= | |
| 7 | g.152648823A>C | CA370198223 | XRCC2 | c.494T>G (p.Ile165Arg) c.662T>G (p.Ile221Arg) n.684T>G | |
| 7 | g.152648823A>G | CA4582313 | XRCC2 | c.494T>C (p.Ile165Thr) c.662T>C (p.Ile221Thr) n.684T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648823A>T | CA370198224 | XRCC2 | c.494T>A (p.Ile165Lys) c.662T>A (p.Ile221Lys) n.684T>A | |
| 7 | g.152648824T>A | CA370198226 | XRCC2 | c.493A>T (p.Ile165Leu) c.661A>T (p.Ile221Leu) n.683A>T | |
| 7 | g.152648824T>C | CA169486943 | XRCC2 | c.493A>G (p.Ile165Val) c.661A>G (p.Ile221Val) n.683A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648824T>G | CA370198225 | XRCC2 | c.493A>C (p.Ile165Leu) c.661A>C (p.Ile221Leu) n.683A>C | |
| 7 | g.152648824T= | CA1753246842 | XRCC2 | c.493A= (p.Ile165=) c.661A= (p.Ile221=) n.683A= | |
| 7 | g.152648825G>A | CA458895319 | XRCC2 | c.492C>T (p.Asp164=) c.660C>T (p.Asp220=) n.682C>T | ClinVar dbSNP gnomAD v4 |
| 7 | g.152648825G>C | CA370198227 | XRCC2 | c.492C>G (p.Asp164Glu) c.660C>G (p.Asp220Glu) n.682C>G | |
| 7 | g.152648825G= | CA1753246845 | XRCC2 | c.492C= (p.Asp164=) c.660C= (p.Asp220=) n.682C= | |
| 7 | g.152648825G>T | CA370198228 | XRCC2 | c.492C>A (p.Asp164Glu) c.660C>A (p.Asp220Glu) n.682C>A | |
| 7 | g.152648826T>A | CA4582314 | XRCC2 | c.491A>T (p.Asp164Val) c.659A>T (p.Asp220Val) n.681A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648826T>C | CA370198229 | XRCC2 | c.491A>G (p.Asp164Gly) c.659A>G (p.Asp220Gly) n.681A>G | ClinVar |
| 7 | g.152648826T>G | CA370198230 | XRCC2 | c.491A>C (p.Asp164Ala) c.659A>C (p.Asp220Ala) n.681A>C | |
| 7 | g.152648826T= | CA1753246849 | XRCC2 | c.491A= (p.Asp164=) c.659A= (p.Asp220=) n.681A= | |
| 7 | g.152648827C>A | CA370198233 | XRCC2 | c.490G>T (p.Asp164Tyr) c.658G>T (p.Asp220Tyr) n.680G>T | |
| 7 | g.152648827C= | CA1753246854 | XRCC2 | c.490G= (p.Asp164=) c.658G= (p.Asp220=) n.680G= | |
| 7 | g.152648827C>G | CA370198231 | XRCC2 | c.490G>C (p.Asp164His) c.658G>C (p.Asp220His) n.680G>C | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648827C>T | CA370198232 | XRCC2 | c.490G>A (p.Asp164Asn) c.658G>A (p.Asp220Asn) n.680G>A | ClinVar dbSNP |
| 7 | g.152648828C>A | CA458895321 | XRCC2 | c.489G>T (p.Val163=) c.657G>T (p.Val219=) n.679G>T | |
| 7 | g.152648828C>G | CA458895322 | XRCC2 | c.489G>C (p.Val163=) c.657G>C (p.Val219=) n.679G>C | |
| 7 | g.152648828C>T | CA458895323 | XRCC2 | c.489G>A (p.Val163=) c.657G>A (p.Val219=) n.679G>A | |
| 7 | g.152648829A>C | CA370198234 | XRCC2 | c.488T>G (p.Val163Gly) c.656T>G (p.Val219Gly) n.678T>G | |
| 7 | g.152648829A>G | CA370198235 | XRCC2 | c.488T>C (p.Val163Ala) c.656T>C (p.Val219Ala) n.678T>C | |
| 7 | g.152648829A>T | CA370198236 | XRCC2 | c.488T>A (p.Val163Glu) c.656T>A (p.Val219Glu) n.678T>A | |
| 7 | g.152648830C>A | CA370198237 | XRCC2 | c.487G>T (p.Val163Leu) c.655G>T (p.Val219Leu) n.677G>T | |
| 7 | g.152648830C= | CA1753246858 | XRCC2 | c.487G= (p.Val163=) c.655G= (p.Val219=) n.677G= | |
| 7 | g.152648830C>G | CA370198238 | XRCC2 | c.487G>C (p.Val163Leu) c.655G>C (p.Val219Leu) n.677G>C | |
| 7 | g.152648830C>T | CA4582315 | XRCC2 | c.487G>A (p.Val163Met) c.655G>A (p.Val219Met) n.677G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648831A>C | CA370198239 | XRCC2 | c.486T>G (p.Asp162Glu) c.654T>G (p.Asp218Glu) n.676T>G | |
| 7 | g.152648831A>G | CA458895325 | XRCC2 | c.486T>C (p.Asp162=) c.654T>C (p.Asp218=) n.676T>C | ClinVar dbSNP gnomAD v4 |
| 7 | g.152648831A>T | CA370198240 | XRCC2 | c.486T>A (p.Asp162Glu) c.654T>A (p.Asp218Glu) n.676T>A | |
| 7 | g.152648832T>A | CA370198241 | XRCC2 | c.485A>T (p.Asp162Val) c.653A>T (p.Asp218Val) n.675A>T | |
| 7 | g.152648832T>C | CA370198243 | XRCC2 | c.485A>G (p.Asp162Gly) c.653A>G (p.Asp218Gly) n.675A>G | ClinVar dbSNP gnomAD v4 |
| 7 | g.152648832T>G | CA370198242 | XRCC2 | c.485A>C (p.Asp162Ala) c.653A>C (p.Asp218Ala) n.675A>C | |
| 7 | g.152648832_152648834delinsTCA | CA1753246865 | XRCC2 | c.483_485delinsTGA (p.Cys161=) c.651_653delinsTGA (p.Cys217=) n.673_675delinsTGA | |
| 7 | g.152648833C>A | CA370198244 | XRCC2 | c.484G>T (p.Asp162Tyr) c.652G>T (p.Asp218Tyr) n.674G>T | |
| 7 | g.152648833C= | CA1753246872 | XRCC2 | c.484G= (p.Asp162=) c.652G= (p.Asp218=) n.674G= | |
| 7 | g.152648833C>G | CA370198245 | XRCC2 | c.484G>C (p.Asp162His) c.652G>C (p.Asp218His) n.674G>C | |
| 7 | g.152648833C>T | CA370198246 | XRCC2 | c.484G>A (p.Asp162Asn) c.652G>A (p.Asp218Asn) n.674G>A | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648837_152648838del | CA16618428 | XRCC2 | c.483_484del (p.Cys161Ter) c.651_652del (p.Cys217Ter) n.673_674del | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648834A= | CA1753246876 | XRCC2 | c.483T= (p.Cys161=) c.651T= (p.Cys217=) n.673T= | |
| 7 | g.152648834A>C | CA370198248 | XRCC2 | c.483T>G (p.Cys161Trp) c.651T>G (p.Cys217Trp) n.673T>G | |
| 7 | g.152648834A>G | CA458895327 | XRCC2 | c.483T>C (p.Cys161=) c.651T>C (p.Cys217=) n.673T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648834A>T | CA370198247 | XRCC2 | c.483T>A (p.Cys161Ter) c.651T>A (p.Cys217Ter) n.673T>A |