Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 | ClinVar 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 | |
7 | g.152648838_152648839insACCAAACACACCCAACACA | CA2778474372 | XRCC2 | c.483_484insTGGGTGTGTTTGGTTGTGT (p.Asp162TrpfsTer7) c.651_652insTGGGTGTGTTTGGTTGTGT (p.Asp218TrpfsTer7) n.673_674insTGGGTGTGTTTGGTTGTGT | |
7 | g.152648835C>A | CA370198249 | XRCC2 | c.482G>T (p.Cys161Phe) c.650G>T (p.Cys217Phe) n.672G>T | |
7 | g.152648835C= | CA1753246879 | XRCC2 | c.482G= (p.Cys161=) c.650G= (p.Cys217=) n.672G= | |
7 | g.152648835C>G | CA370198250 | XRCC2 | c.482G>C (p.Cys161Ser) c.650G>C (p.Cys217Ser) n.672G>C | dbSNP |
7 | g.152648835C>T | CA10584276 | XRCC2 | c.482G>A (p.Cys161Tyr) c.650G>A (p.Cys217Tyr) n.672G>A | ClinVar dbSNP |
7 | g.152648836A= | CA1753246882 | XRCC2 | c.481T= (p.Cys161=) c.649T= (p.Cys217=) n.671T= | |
7 | g.152648836A>C | CA370198251 | XRCC2 | c.481T>G (p.Cys161Gly) c.649T>G (p.Cys217Gly) n.671T>G | |
7 | g.152648836A>G | CA370198252 | XRCC2 | c.481T>C (p.Cys161Arg) c.649T>C (p.Cys217Arg) n.671T>C | dbSNP |
7 | g.152648836A>T | CA370198253 | XRCC2 | c.481T>A (p.Cys161Ser) c.649T>A (p.Cys217Ser) n.671T>A | gnomAD v4 |
7 | g.152648837C>A | CA458895330 | XRCC2 | c.480G>T (p.Leu160=) c.648G>T (p.Leu216=) n.670G>T | ClinVar |
7 | g.152648837C>G | CA458895331 | XRCC2 | c.480G>C (p.Leu160=) c.648G>C (p.Leu216=) n.670G>C | |
7 | g.152648837C>T | CA458895332 | XRCC2 | c.480G>A (p.Leu160=) c.648G>A (p.Leu216=) n.670G>A | ClinVar gnomAD v4 |
7 | g.152648837_152648847delinsCAGTCGTCGAG | CA1753246884 | XRCC2 | c.470_480delinsCTCGACGACTG (p.Ser157=) c.638_648delinsCTCGACGACTG (p.Ser213=) n.660_670delinsCTCGACGACTG | |
7 | g.152648838A= | CA1753246887 | XRCC2 | c.479T= (p.Leu160=) c.647T= (p.Leu216=) n.669T= | |
7 | g.152648838A>C | CA370198254 | XRCC2 | c.479T>G (p.Leu160Arg) c.647T>G (p.Leu216Arg) n.669T>G | |
7 | g.152648838A>G | CA370198255 | XRCC2 | c.479T>C (p.Leu160Pro) c.647T>C (p.Leu216Pro) n.669T>C | ClinVar dbSNP gnomAD v4 |
7 | g.152648838A>T | CA370198256 | XRCC2 | c.479T>A (p.Leu160Gln) c.647T>A (p.Leu216Gln) n.669T>A | |
7 | g.152648840_152648849del | CA579080840 | XRCC2 | c.470_479del (p.Ser157CysfsTer6) c.638_647del (p.Ser213CysfsTer6) n.660_669del | dbSNP gnomAD v2 gnomAD v4 |
7 | g.152648839G>A | CA458895333 | XRCC2 | c.478C>T (p.Leu160=) c.646C>T (p.Leu216=) n.668C>T | |
7 | g.152648839G>C | CA370198257 | XRCC2 | c.478C>G (p.Leu160Val) c.646C>G (p.Leu216Val) n.668C>G | dbSNP |