| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.152648612_152648662del | CA2685735740 | XRCC2 | c.656_*31del (n.[c.656_*31del;Ser219ThrfsTer?]) c.824_*31del (n.[c.824_*31del;Ser275ThrfsTer?]) n.846_896del | gnomAD v4 |
| 7 | g.152648625_152648635del | CA2685735748 | XRCC2 | c.*9_*19del (n.*9_*19del) n.874_884del | gnomAD v4 |
| 7 | g.152648631del | CA2685735750 | XRCC2 | c.*14del (n.*14del) n.879del | gnomAD v4 |
| 7 | g.152648644_152648645insTATACATCATATGTATATGATACATGATATGATGTATATCA | CA2778474324 | XRCC2 | c.*11_*12insTCATGTATCATATACATATGATGTATATGATATACATCATA (n.*11_*12insTCATGTATCATATACATATGATGTATATGATATACATCATA) n.876_877insTCATGTATCATATACATATGATGTATATGATATACATCATA | |
| 7 | g.152648632A= | CA1753246462 | XRCC2 | c.*10T= (n.*10T=) n.875T= | |
| 7 | g.152648632A>C | CA2685735752 | XRCC2 | c.*10T>G (n.*10T>G) n.875T>G | gnomAD v4 |
| 7 | g.152648632A>G | CA1753246463 | XRCC2 | c.*10T>C (n.*10T>C) n.875T>C | dbSNP gnomAD v4 |
| 7 | g.152648632A>T | CA2685735751 | XRCC2 | c.*10T>A (n.*10T>A) n.875T>A | gnomAD v4 |
| 7 | g.152648633T>C | CA4582277 | XRCC2 | c.*9A>G (n.*9A>G) n.874A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648633T= | CA1753246464 | XRCC2 | c.*9A= (n.*9A=) n.874A= | |
| 7 | g.152648634G>T | CA2685735753 | XRCC2 | c.*8C>A (n.*8C>A) n.873C>A | gnomAD v4 |
| 7 | g.152648635A= | CA1753246465 | XRCC2 | c.*7T= (n.*7T=) n.872T= | |
| 7 | g.152648635A>C | CA2579071947 | XRCC2 | c.*7T>G (n.*7T>G) n.872T>G | |
| 7 | g.152648635A>G | CA4582278 | XRCC2 | c.*7T>C (n.*7T>C) n.872T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648636T>C | CA1108857531 | XRCC2 | c.*6A>G (n.*6A>G) n.871A>G | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648636T>G | CA2685735754 | XRCC2 | c.*6A>C (n.*6A>C) n.871A>C | gnomAD v4 |
| 7 | g.152648636T= | CA1753246468 | XRCC2 | c.*6A= (n.*6A=) n.871A= | |
| 7 | g.152648637G>A | CA2579071948 | XRCC2 | c.*5C>T (n.*5C>T) n.870C>T | |
| 7 | g.152648638T>C | CA4582279 | XRCC2 | c.*4A>G (n.*4A>G) n.869A>G | dbSNP ExAC gnomAD v4 |
| 7 | g.152648638T= | CA1753246470 | XRCC2 | c.*4A= (n.*4A=) n.869A= | |
| 7 | g.152648639A= | CA1753246472 | XRCC2 | c.*3T= (n.*3T=) n.868T= | |
| 7 | g.152648639A>G | CA4582280 | XRCC2 | c.*3T>C (n.*3T>C) n.868T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648640T>C | CA2685735755 | XRCC2 | c.*2A>G (n.*2A>G) n.867A>G | gnomAD v4 |
| 7 | g.152648641A= | CA1753246474 | XRCC2 | c.*1T= (n.*1T=) n.866T= | |
| 7 | g.152648641A>G | CA4582281 | XRCC2 | c.*1T>C (n.*1T>C) n.866T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648641A>T | CA4582282 | XRCC2 | c.*1T>A (n.*1T>A) n.866T>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648642T>A | CA370197812 | XRCC2 | c.675A>T (p.Ter225Cys) c.843A>T (p.Ter281Cys) n.865A>T | |
| 7 | g.152648642T>C | CA370197813 | XRCC2 | c.675A>G (p.Ter225Trp) c.843A>G (p.Ter281Trp) n.865A>G | |
| 7 | g.152648642T>G | CA370197814 | XRCC2 | c.675A>C (p.Ter225Cys) c.843A>C (p.Ter281Cys) n.865A>C | |
| 7 | g.152648647_152648656del | CA2580077731 | XRCC2 | c.666_675del (p.Glu222AspfsTer16) c.834_843del (p.Glu278AspfsTer16) n.856_865del | ClinVar |
| 7 | g.152648643C>A | CA370197815 | XRCC2 | c.674G>T (p.Ter225Leu) c.842G>T (p.Ter281Leu) n.864G>T | |
| 7 | g.152648643C= | CA1753246475 | XRCC2 | c.674G= (p.Ter225=) c.842G= (p.Ter281=) n.864G= | |
| 7 | g.152648643C>G | CA370197816 | XRCC2 | c.674G>C (p.Ter225Ser) c.842G>C (p.Ter281Ser) n.864G>C | |
| 7 | g.152648643C>T | CA4582283 | XRCC2 | c.674G>A (p.Ter225=) c.842G>A (p.Ter281=) n.864G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648644A>C | CA370197817 | XRCC2 | c.673T>G (p.Ter225Gly) c.841T>G (p.Ter281Gly) n.863T>G | |
| 7 | g.152648644A>G | CA370197818 | XRCC2 | c.673T>C (p.Ter225Arg) c.841T>C (p.Ter281Arg) n.863T>C | |
| 7 | g.152648644A>T | CA370197819 | XRCC2 | c.673T>A (p.Ter225Arg) c.841T>A (p.Ter281Arg) n.863T>A | |
| 7 | g.152648645A= | CA1753246478 | XRCC2 | c.672T= (p.Cys224=) c.840T= (p.Cys280=) n.862T= | |
| 7 | g.152648645A>C | CA370197820 | XRCC2 | c.672T>G (p.Cys224Trp) c.840T>G (p.Cys280Trp) n.862T>G | |
| 7 | g.152648645A>G | CA458895045 | XRCC2 | c.672T>C (p.Cys224=) c.840T>C (p.Cys280=) n.862T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648645A>T | CA370197821 | XRCC2 | c.672T>A (p.Cys224Ter) c.840T>A (p.Cys280Ter) n.862T>A | |
| 7 | g.152648646C>A | CA370197824 | XRCC2 | c.671G>T (p.Cys224Phe) c.839G>T (p.Cys280Phe) n.861G>T | dbSNP gnomAD v4 |
| 7 | g.152648646C= | CA1753246482 | XRCC2 | c.671G= (p.Cys224=) c.839G= (p.Cys280=) n.861G= | |
| 7 | g.152648646C>G | CA370197823 | XRCC2 | c.671G>C (p.Cys224Ser) c.839G>C (p.Cys280Ser) n.861G>C | |
| 7 | g.152648646C>T | CA370197822 | XRCC2 | c.671G>A (p.Cys224Tyr) c.839G>A (p.Cys280Tyr) n.861G>A | ClinVar |
| 7 | g.152648647A= | CA1753246483 | XRCC2 | c.670T= (p.Cys224=) c.838T= (p.Cys280=) n.860T= | |
| 7 | g.152648647A>C | CA370197825 | XRCC2 | c.670T>G (p.Cys224Gly) c.838T>G (p.Cys280Gly) n.860T>G | |
| 7 | g.152648647A>G | CA4582284 | XRCC2 | c.670T>C (p.Cys224Arg) c.838T>C (p.Cys280Arg) n.860T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648647A>T | CA370197826 | XRCC2 | c.670T>A (p.Cys224Ser) c.838T>A (p.Cys280Ser) n.860T>A | |
| 7 | g.152648648A>C | CA370197827 | XRCC2 | c.669T>G (p.Phe223Leu) c.837T>G (p.Phe279Leu) n.859T>G | |
| 7 | g.152648648A>G | CA458895047 | XRCC2 | c.669T>C (p.Phe223=) c.837T>C (p.Phe279=) n.859T>C | |
| 7 | g.152648648A>T | CA370197828 | XRCC2 | c.669T>A (p.Phe223Leu) c.837T>A (p.Phe279Leu) n.859T>A | |
| 7 | g.152648649A>C | CA370197829 | XRCC2 | c.668T>G (p.Phe223Cys) c.836T>G (p.Phe279Cys) n.858T>G | |
| 7 | g.152648649A>G | CA370197830 | XRCC2 | c.668T>C (p.Phe223Ser) c.836T>C (p.Phe279Ser) n.858T>C | |
| 7 | g.152648649A>T | CA370197831 | XRCC2 | c.668T>A (p.Phe223Tyr) c.836T>A (p.Phe279Tyr) n.858T>A | |
| 7 | g.152648650A>C | CA370197832 | XRCC2 | c.667T>G (p.Phe223Val) c.835T>G (p.Phe279Val) n.857T>G | |
| 7 | g.152648650A>G | CA370197833 | XRCC2 | c.667T>C (p.Phe223Leu) c.835T>C (p.Phe279Leu) n.857T>C | |
| 7 | g.152648650A>T | CA370197834 | XRCC2 | c.667T>A (p.Phe223Ile) c.835T>A (p.Phe279Ile) n.857T>A | COSMIC |
| 7 | g.152648651T>A | CA370197835 | XRCC2 | c.666A>T (p.Glu222Asp) c.834A>T (p.Glu278Asp) n.856A>T | |
| 7 | g.152648651T>C | CA458895049 | XRCC2 | c.666A>G (p.Glu222=) c.834A>G (p.Glu278=) n.856A>G | ClinVar gnomAD v4 |
| 7 | g.152648651T>G | CA370197836 | XRCC2 | c.666A>C (p.Glu222Asp) c.834A>C (p.Glu278Asp) n.856A>C | |
| 7 | g.152648652T>A | CA370197838 | XRCC2 | c.665A>T (p.Glu222Val) c.833A>T (p.Glu278Val) n.855A>T | |
| 7 | g.152648652T>C | CA370197839 | XRCC2 | c.665A>G (p.Glu222Gly) c.833A>G (p.Glu278Gly) n.855A>G | ClinVar |
| 7 | g.152648652T>G | CA370197837 | XRCC2 | c.665A>C (p.Glu222Ala) c.833A>C (p.Glu278Ala) n.855A>C | |
| 7 | g.152648653C>A | CA370197840 | XRCC2 | c.664G>T (p.Glu222Ter) c.832G>T (p.Glu278Ter) n.854G>T | |
| 7 | g.152648653C>G | CA370197841 | XRCC2 | c.664G>C (p.Glu222Gln) c.832G>C (p.Glu278Gln) n.854G>C | |
| 7 | g.152648653C>T | CA370197842 | XRCC2 | c.664G>A (p.Glu222Lys) c.832G>A (p.Glu278Lys) n.854G>A | ClinVar dbSNP |
| 7 | g.152648654A>C | CA458895053 | XRCC2 | c.663T>G (p.Val221=) c.831T>G (p.Val277=) n.853T>G | |
| 7 | g.152648654A>G | CA458895054 | XRCC2 | c.663T>C (p.Val221=) c.831T>C (p.Val277=) n.853T>C | |
| 7 | g.152648654A>T | CA458895055 | XRCC2 | c.663T>A (p.Val221=) c.831T>A (p.Val277=) n.853T>A | |
| 7 | g.152648655A>C | CA370197843 | XRCC2 | c.662T>G (p.Val221Gly) c.830T>G (p.Val277Gly) n.852T>G | |
| 7 | g.152648655A>G | CA370197844 | XRCC2 | c.662T>C (p.Val221Ala) c.830T>C (p.Val277Ala) n.852T>C | |
| 7 | g.152648655A>T | CA370197845 | XRCC2 | c.662T>A (p.Val221Asp) c.830T>A (p.Val277Asp) n.852T>A | |
| 7 | g.152648655_152648656delinsAC | CA1753246485 | XRCC2 | c.661_662delinsGT (p.Val221=) c.829_830delinsGT (p.Val277=) n.851_852delinsGT | |
| 7 | g.152648656C>A | CA370197846 | XRCC2 | c.661G>T (p.Val221Phe) c.829G>T (p.Val277Phe) n.851G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648656C= | CA1753246487 | XRCC2 | c.661G= (p.Val221=) c.829G= (p.Val277=) n.851G= | |
| 7 | g.152648656C>G | CA370197847 | XRCC2 | c.661G>C (p.Val221Leu) c.829G>C (p.Val277Leu) n.851G>C | |
| 7 | g.152648656C>T | CA4582286 | XRCC2 | c.661G>A (p.Val221Ile) c.829G>A (p.Val277Ile) n.851G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648659del | CA4582285 | XRCC2 | c.661del (p.Val221LeufsTer20) c.829del (p.Val277LeufsTer20) n.851del | dbSNP ExAC gnomAD v2 |
| 7 | g.152648657C>A | CA458895063 | XRCC2 | c.660G>T (p.Gly220=) c.828G>T (p.Gly276=) n.850G>T | dbSNP gnomAD v4 |
| 7 | g.152648657C= | CA1753246491 | XRCC2 | c.660G= (p.Gly220=) c.828G= (p.Gly276=) n.850G= | |
| 7 | g.152648657C>G | CA458895061 | XRCC2 | c.660G>C (p.Gly220=) c.828G>C (p.Gly276=) n.850G>C | ClinVar gnomAD v4 |
| 7 | g.152648657C>T | CA458895059 | XRCC2 | c.660G>A (p.Gly220=) c.828G>A (p.Gly276=) n.850G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648658C>A | CA370197848 | XRCC2 | c.659G>T (p.Gly220Val) c.827G>T (p.Gly276Val) n.849G>T | dbSNP gnomAD v4 |
| 7 | g.152648658C>G | CA370197849 | XRCC2 | c.659G>C (p.Gly220Ala) c.827G>C (p.Gly276Ala) n.849G>C | COSMIC |
| 7 | g.152648658C>T | CA370197850 | XRCC2 | c.659G>A (p.Gly220Glu) c.827G>A (p.Gly276Glu) n.849G>A | ClinVar |
| 7 | g.152648659C>A | CA370197852 | XRCC2 | c.658G>T (p.Gly220Trp) c.826G>T (p.Gly276Trp) n.848G>T | |
| 7 | g.152648659C= | CA1753246495 | XRCC2 | c.658G= (p.Gly220=) c.826G= (p.Gly276=) n.848G= | |
| 7 | g.152648659C>G | CA370197851 | XRCC2 | c.658G>C (p.Gly220Arg) c.826G>C (p.Gly276Arg) n.848G>C | |
| 7 | g.152648659C>T | CA300481 | XRCC2 | c.658G>A (p.Gly220Arg) c.826G>A (p.Gly276Arg) n.848G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648660_152648661del | CA2685735756 | XRCC2 | c.657_658del (p.Ser219ArgfsTer3) c.825_826del (p.Ser275ArgfsTer3) n.847_848del | gnomAD v4 |
| 7 | g.152648660A= | CA1753246500 | XRCC2 | c.657T= (p.Ser219=) c.825T= (p.Ser275=) n.847T= | |
| 7 | g.152648660A>C | CA4582288 | XRCC2 | c.657T>G (p.Ser219Arg) c.825T>G (p.Ser275Arg) n.847T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648660A>G | CA4582287 | XRCC2 | c.657T>C (p.Ser219=) c.825T>C (p.Ser275=) n.847T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648660A>T | CA370197853 | XRCC2 | c.657T>A (p.Ser219Arg) c.825T>A (p.Ser275Arg) n.847T>A | |
| 7 | g.152648661C>A | CA370197854 | XRCC2 | c.656G>T (p.Ser219Ile) c.824G>T (p.Ser275Ile) n.846G>T | |
| 7 | g.152648661C>G | CA370197855 | XRCC2 | c.656G>C (p.Ser219Thr) c.824G>C (p.Ser275Thr) n.846G>C | |
| 7 | g.152648661C>T | CA370197856 | XRCC2 | c.656G>A (p.Ser219Asn) c.824G>A (p.Ser275Asn) n.846G>A | |
| 7 | g.152648662T>A | CA370197857 | XRCC2 | c.655A>T (p.Ser219Cys) c.823A>T (p.Ser275Cys) n.845A>T | |
| 7 | g.152648662T>C | CA370197858 | XRCC2 | c.655A>G (p.Ser219Gly) c.823A>G (p.Ser275Gly) n.845A>G | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648662T>G | CA370197859 | XRCC2 | c.655A>C (p.Ser219Arg) c.823A>C (p.Ser275Arg) n.845A>C | |
| 7 | g.152648662T= | CA1753246503 | XRCC2 | c.655A= (p.Ser219=) c.823A= (p.Ser275=) n.845A= | |
| 7 | g.152648662_152648663insGGC | CA2685735757 | XRCC2 | c.654_655insGCC (p.Glu218_Ser219insAla) c.822_823insGCC (p.Glu274_Ser275insAla) n.844_845insGCC | gnomAD v4 |
| 7 | g.152648662_152648663insGGCTGGGCGCGGTGGC | CA2685735758 | XRCC2 | c.654_655insGCCACCGCGCCCAGCC (p.Ser219AlafsTer9) c.822_823insGCCACCGCGCCCAGCC (p.Ser275AlafsTer9) n.844_845insGCCACCGCGCCCAGCC | gnomAD v4 |
| 7 | g.152648663T>A | CA370197860 | XRCC2 | c.654A>T (p.Glu218Asp) c.822A>T (p.Glu274Asp) n.844A>T | |
| 7 | g.152648663T>C | CA458895066 | XRCC2 | c.654A>G (p.Glu218=) c.822A>G (p.Glu274=) n.844A>G | |
| 7 | g.152648663T>G | CA4582289 | XRCC2 | c.654A>C (p.Glu218Asp) c.822A>C (p.Glu274Asp) n.844A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648663T= | CA1753246504 | XRCC2 | c.654A= (p.Glu218=) c.822A= (p.Glu274=) n.844A= | |
| 7 | g.152648663_152648664insGGGCGCGGTGGC | CA2685735759 | XRCC2 | c.653_654insGCCACCGCGCCC (p.Glu218_Ser219insProProArgPro) c.821_822insGCCACCGCGCCC (p.Glu274_Ser275insProProArgPro) n.843_844insGCCACCGCGCCC | gnomAD v4 |
| 7 | g.152648664T>A | CA370197861 | XRCC2 | c.653A>T (p.Glu218Val) c.821A>T (p.Glu274Val) n.843A>T | |
| 7 | g.152648664T>C | CA16618423 | XRCC2 | c.653A>G (p.Glu218Gly) c.821A>G (p.Glu274Gly) n.843A>G | ClinVar dbSNP gnomAD v4 |
| 7 | g.152648664T>G | CA370197862 | XRCC2 | c.653A>C (p.Glu218Ala) c.821A>C (p.Glu274Ala) n.843A>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648664T= | CA1753246508 | XRCC2 | c.653A= (p.Glu218=) c.821A= (p.Glu274=) n.843A= | |
| 7 | g.152648666_152648667dup | CA658823261 | XRCC2 | c.652_653dup (p.Ser219LysfsTer23) c.820_821dup (p.Ser275LysfsTer23) n.842_843dup | ClinVar dbSNP gnomAD v4 |
| 7 | g.152648665C>A | CA370197864 | XRCC2 | c.652G>T (p.Glu218Ter) c.820G>T (p.Glu274Ter) n.842G>T | |
| 7 | g.152648665C>G | CA370197865 | XRCC2 | c.652G>C (p.Glu218Gln) c.820G>C (p.Glu274Gln) n.842G>C | |
| 7 | g.152648665C>T | CA370197863 | XRCC2 | c.652G>A (p.Glu218Lys) c.820G>A (p.Glu274Lys) n.842G>A | dbSNP |
| 7 | g.152648665_152648666insACGCCTGTAA | CA2685735760 | XRCC2 | c.651_652insTTACAGGCGT (p.Glu218LeufsTer4) c.819_820insTTACAGGCGT (p.Glu274LeufsTer4) n.841_842insTTACAGGCGT | gnomAD v4 |
| 7 | g.152648666T>A | CA458895071 | XRCC2 | c.651A>T (p.Gly217=) c.819A>T (p.Gly273=) n.841A>T | |
| 7 | g.152648666T>C | CA458895073 | XRCC2 | c.651A>G (p.Gly217=) c.819A>G (p.Gly273=) n.841A>G | |
| 7 | g.152648666T>G | CA458895072 | XRCC2 | c.651A>C (p.Gly217=) c.819A>C (p.Gly273=) n.841A>C | |
| 7 | g.152648666T= | CA1753246509 | XRCC2 | c.651A= (p.Gly217=) c.819A= (p.Gly273=) n.841A= | |
| 7 | g.152648666_152648667insGGGCG | CA2685735761 | XRCC2 | c.650_651insCGCCC (p.Glu218AlafsTer25) c.818_819insCGCCC (p.Glu274AlafsTer25) n.840_841insCGCCC | gnomAD v4 |
| 7 | g.152648666_152648667insGGGCGCGGTGG | CA2685735762 | XRCC2 | c.650_651insCCACCGCGCCC (p.Glu218HisfsTer27) c.818_819insCCACCGCGCCC (p.Glu274HisfsTer27) n.840_841insCCACCGCGCCC | gnomAD v4 |
| 7 | g.152648666_152648667insGGGCGCGGTGGCTCACG | CA2685735763 | XRCC2 | c.650_651insCGTGAGCCACCGCGCCC (p.Glu218ValfsTer29) c.818_819insCGTGAGCCACCGCGCCC (p.Glu274ValfsTer29) n.840_841insCGTGAGCCACCGCGCCC | gnomAD v4 |
| 7 | g.152648666_152648667insGGGCGCGGTGGCTCACGCCTGTAATC | CA2685735764 | XRCC2 | c.650_651insGATTACAGGCGTGAGCCACCGCGCCC (p.Glu218IlefsTer32) c.818_819insGATTACAGGCGTGAGCCACCGCGCCC (p.Glu274IlefsTer32) n.840_841insGATTACAGGCGTGAGCCACCGCGCCC | gnomAD v4 |
| 7 | g.152648666_152648667insGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGG | CA579080835 | XRCC2 | c.650_651insCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCC (p.Gly217_Glu218insLeuGlyLeuProLysCysTrpAspTyrArgArgGluProProArgPro) c.818_819insCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCC (p.Gly273_Glu274insLeuGlyLeuProLysCysTrpAspTyrArgArgGluProProArgPro) n.840_841insCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCC | dbSNP gnomAD v2 |
| 7 | g.152648667C>A | CA370197866 | XRCC2 | c.650G>T (p.Gly217Val) c.818G>T (p.Gly273Val) n.840G>T | |
| 7 | g.152648667C>G | CA370197867 | XRCC2 | c.650G>C (p.Gly217Ala) c.818G>C (p.Gly273Ala) n.840G>C | COSMIC |
| 7 | g.152648667C>T | CA370197868 | XRCC2 | c.650G>A (p.Gly217Glu) c.818G>A (p.Gly273Glu) n.840G>A | ClinVar dbSNP |
| 7 | g.152648668C>A | CA370197869 | XRCC2 | c.649G>T (p.Gly217Ter) c.817G>T (p.Gly273Ter) n.839G>T | |
| 7 | g.152648668C= | CA1753246517 | XRCC2 | c.649G= (p.Gly217=) c.817G= (p.Gly273=) n.839G= | |
| 7 | g.152648668C>G | CA370197870 | XRCC2 | c.649G>C (p.Gly217Arg) c.817G>C (p.Gly273Arg) n.839G>C | |
| 7 | g.152648668C>T | CA370197871 | XRCC2 | c.649G>A (p.Gly217Arg) c.817G>A (p.Gly273Arg) n.839G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648668_152648671delinsCAAT | CA1753246516 | XRCC2 | c.646_649delinsATTG (p.Ile216=) c.814_817delinsATTG (p.Ile272=) n.836_839delinsATTG | |
| 7 | g.152648669A>C | CA370197872 | XRCC2 | c.648T>G (p.Ile216Met) c.816T>G (p.Ile272Met) n.838T>G | |
| 7 | g.152648669A>G | CA458895077 | XRCC2 | c.648T>C (p.Ile216=) c.816T>C (p.Ile272=) n.838T>C | |
| 7 | g.152648669A>T | CA458895079 | XRCC2 | c.648T>A (p.Ile216=) c.816T>A (p.Ile272=) n.838T>A | gnomAD v4 |
| 7 | g.152648674_152648676del | CA1108857565 | XRCC2 | c.646_648del (p.Ile216del) c.814_816del (p.Ile272del) n.836_838del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648670A>C | CA370197873 | XRCC2 | c.647T>G (p.Ile216Ser) c.815T>G (p.Ile272Ser) n.837T>G | |
| 7 | g.152648670A>G | CA370197875 | XRCC2 | c.647T>C (p.Ile216Thr) c.815T>C (p.Ile272Thr) n.837T>C | gnomAD v4 |
| 7 | g.152648670A>T | CA370197874 | XRCC2 | c.647T>A (p.Ile216Asn) c.815T>A (p.Ile272Asn) n.837T>A | |
| 7 | g.152648671T>A | CA370197876 | XRCC2 | c.646A>T (p.Ile216Phe) c.814A>T (p.Ile272Phe) n.836A>T | dbSNP |
| 7 | g.152648671T>C | CA370197877 | XRCC2 | c.646A>G (p.Ile216Val) c.814A>G (p.Ile272Val) n.836A>G | gnomAD v4 |
| 7 | g.152648671T>G | CA370197878 | XRCC2 | c.646A>C (p.Ile216Leu) c.814A>C (p.Ile272Leu) n.836A>C | |
| 7 | g.152648672A>C | CA370197879 | XRCC2 | c.645T>G (p.Ile215Met) c.813T>G (p.Ile271Met) n.835T>G | |
| 7 | g.152648672A>G | CA458895084 | XRCC2 | c.645T>C (p.Ile215=) c.813T>C (p.Ile271=) n.835T>C | |
| 7 | g.152648672A>T | CA458895083 | XRCC2 | c.645T>A (p.Ile215=) c.813T>A (p.Ile271=) n.835T>A | |
| 7 | g.152648673A>C | CA370197880 | XRCC2 | c.644T>G (p.Ile215Ser) c.812T>G (p.Ile271Ser) n.834T>G | |
| 7 | g.152648673A>G | CA370197882 | XRCC2 | c.644T>C (p.Ile215Thr) c.812T>C (p.Ile271Thr) n.834T>C | |
| 7 | g.152648673A>T | CA370197881 | XRCC2 | c.644T>A (p.Ile215Asn) c.812T>A (p.Ile271Asn) n.834T>A | |
| 7 | g.152648674T>A | CA370197883 | XRCC2 | c.643A>T (p.Ile215Phe) c.811A>T (p.Ile271Phe) n.833A>T | |
| 7 | g.152648674T>C | CA288153 | XRCC2 | c.643A>G (p.Ile215Val) c.811A>G (p.Ile271Val) n.833A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648674T>G | CA370197884 | XRCC2 | c.643A>C (p.Ile215Leu) c.811A>C (p.Ile271Leu) n.833A>C | |
| 7 | g.152648674T= | CA1753246523 | XRCC2 | c.643A= (p.Ile215=) c.811A= (p.Ile271=) n.833A= | |
| 7 | g.152648674_152648677delinsTAAA | CA1753246524 | XRCC2 | c.640_643delinsTTTA (p.Phe214=) c.808_811delinsTTTA (p.Phe270=) n.830_833delinsTTTA | |
| 7 | g.152648675A>C | CA370197885 | XRCC2 | c.642T>G (p.Phe214Leu) c.810T>G (p.Phe270Leu) n.832T>G | |
| 7 | g.152648675A>G | CA458895088 | XRCC2 | c.642T>C (p.Phe214=) c.810T>C (p.Phe270=) n.832T>C | |
| 7 | g.152648675A>T | CA370197886 | XRCC2 | c.642T>A (p.Phe214Leu) c.810T>A (p.Phe270Leu) n.832T>A | |
| 7 | g.152648681dup | CA16618424 | XRCC2 | c.642dup (p.Ile215TyrfsTer8) c.810dup (p.Ile271TyrfsTer8) n.832dup | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648681del | CA2685735765 | XRCC2 | c.642del (p.Phe214LeufsTer27) c.810del (p.Phe270LeufsTer27) n.832del | dbSNP gnomAD v4 |
| 7 | g.152648679_152648681del | CA300488 | XRCC2 | c.640_642del (p.Phe214del) c.808_810del (p.Phe270del) n.830_832del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648676A>C | CA370197887 | XRCC2 | c.641T>G (p.Phe214Cys) c.809T>G (p.Phe270Cys) n.831T>G | ClinVar |
| 7 | g.152648676A>G | CA370197888 | XRCC2 | c.641T>C (p.Phe214Ser) c.809T>C (p.Phe270Ser) n.831T>C | |
| 7 | g.152648676A>T | CA370197889 | XRCC2 | c.641T>A (p.Phe214Tyr) c.809T>A (p.Phe270Tyr) n.831T>A | |
| 7 | g.152648677A= | CA1753246532 | XRCC2 | c.640T= (p.Phe214=) c.808T= (p.Phe270=) n.830T= | |
| 7 | g.152648677A>C | CA288151 | XRCC2 | c.640T>G (p.Phe214Val) c.808T>G (p.Phe270Val) n.830T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648677A>G | CA370197891 | XRCC2 | c.640T>C (p.Phe214Leu) c.808T>C (p.Phe270Leu) n.830T>C | |
| 7 | g.152648677A>T | CA370197890 | XRCC2 | c.640T>A (p.Phe214Ile) c.808T>A (p.Phe270Ile) n.830T>A | |
| 7 | g.152648678A>C | CA370197892 | XRCC2 | c.639T>G (p.Phe213Leu) c.807T>G (p.Phe269Leu) n.829T>G | ClinVar |
| 7 | g.152648678A>G | CA458895090 | XRCC2 | c.639T>C (p.Phe213=) c.807T>C (p.Phe269=) n.829T>C | |
| 7 | g.152648678A>T | CA370197893 | XRCC2 | c.639T>A (p.Phe213Leu) c.807T>A (p.Phe269Leu) n.829T>A | |
| 7 | g.152648679A>C | CA370197894 | XRCC2 | c.638T>G (p.Phe213Cys) c.806T>G (p.Phe269Cys) n.828T>G | |
| 7 | g.152648679A>G | CA370197895 | XRCC2 | c.638T>C (p.Phe213Ser) c.806T>C (p.Phe269Ser) n.828T>C | |
| 7 | g.152648679A>T | CA370197896 | XRCC2 | c.638T>A (p.Phe213Tyr) c.806T>A (p.Phe269Tyr) n.828T>A | |
| 7 | g.152648679_152648731del | CA2685735766 | XRCC2 | c.586_638del (p.Gln196PhefsTer9) c.754_806del (p.Gln252PhefsTer9) n.776_828del | gnomAD v4 |
| 7 | g.152648680A= | CA1753246534 | XRCC2 | c.637T= (p.Phe213=) c.805T= (p.Phe269=) n.827T= | |
| 7 | g.152648680A>C | CA370197897 | XRCC2 | c.637T>G (p.Phe213Val) c.805T>G (p.Phe269Val) n.827T>G | |
| 7 | g.152648680A>G | CA370197898 | XRCC2 | c.637T>C (p.Phe213Leu) c.805T>C (p.Phe269Leu) n.827T>C | ClinVar |
| 7 | g.152648680A>T | CA4582290 | XRCC2 | c.637T>A (p.Phe213Ile) c.805T>A (p.Phe269Ile) n.827T>A | ClinVar dbSNP ExAC gnomAD v2 |
| 7 | g.152648681A>C | CA370197899 | XRCC2 | c.636T>G (p.His212Gln) c.804T>G (p.His268Gln) n.826T>G | |
| 7 | g.152648681A>G | CA458895093 | XRCC2 | c.636T>C (p.His212=) c.804T>C (p.His268=) n.826T>C | |
| 7 | g.152648681A>T | CA370197900 | XRCC2 | c.636T>A (p.His212Gln) c.804T>A (p.His268Gln) n.826T>A | ClinVar |
| 7 | g.152648681_152648682delinsAT | CA1753246537 | XRCC2 | c.635_636delinsAT (p.His212=) c.803_804delinsAT (p.His268=) n.825_826delinsAT | |
| 7 | g.152648681_152648684delinsATGT | CA1753246538 | XRCC2 | c.633_636delinsACAT (p.Lys211=) c.801_804delinsACAT (p.Lys267=) n.823_826delinsACAT | |
| 7 | g.152648682del | CA4582291 | XRCC2 | c.635del (p.His212LeufsTer29) c.803del (p.His268LeufsTer29) n.825del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648682T>A | CA370197901 | XRCC2 | c.635A>T (p.His212Leu) c.803A>T (p.His268Leu) n.825A>T | |
| 7 | g.152648682T>C | CA370197903 | XRCC2 | c.635A>G (p.His212Arg) c.803A>G (p.His268Arg) n.825A>G | |
| 7 | g.152648682T>G | CA370197902 | XRCC2 | c.635A>C (p.His212Pro) c.803A>C (p.His268Pro) n.825A>C | |
| 7 | g.152648683_152648685del | CA915945586 | XRCC2 | c.633_635del (p.Lys211_His212delinsAsn) c.801_803del (p.Lys267_His268delinsAsn) n.823_825del | ClinVar dbSNP |
| 7 | g.152648683G>A | CA370197904 | XRCC2 | c.634C>T (p.His212Tyr) c.802C>T (p.His268Tyr) n.824C>T | ClinVar |
| 7 | g.152648683G>C | CA370197905 | XRCC2 | c.634C>G (p.His212Asp) c.802C>G (p.His268Asp) n.824C>G | |
| 7 | g.152648683G>T | CA370197906 | XRCC2 | c.634C>A (p.His212Asn) c.802C>A (p.His268Asn) n.824C>A | |
| 7 | g.152648683_152648684delinsGT | CA1753246542 | XRCC2 | c.633_634delinsAC (p.Lys211=) c.801_802delinsAC (p.Lys267=) n.823_824delinsAC | |
| 7 | g.152648684T>A | CA370197908 | XRCC2 | c.633A>T (p.Lys211Asn) c.801A>T (p.Lys267Asn) n.823A>T | |
| 7 | g.152648684T>C | CA458895100 | XRCC2 | c.633A>G (p.Lys211=) c.801A>G (p.Lys267=) n.823A>G | ClinVar dbSNP |
| 7 | g.152648684T>G | CA370197907 | XRCC2 | c.633A>C (p.Lys211Asn) c.801A>C (p.Lys267Asn) n.823A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648684T= | CA1753246544 | XRCC2 | c.633A= (p.Lys211=) c.801A= (p.Lys267=) n.823A= | |
| 7 | g.152648690dup | CA4582292 | XRCC2 | c.633dup (p.His212ThrfsTer11) c.801dup (p.His268ThrfsTer11) n.823dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648690del | CA458895101 | XRCC2 | c.633del (p.Lys211AsnfsTer30) c.801del (p.Lys267AsnfsTer30) n.823del | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.152648685T>A | CA370197909 | XRCC2 | c.632A>T (p.Lys211Ile) c.800A>T (p.Lys267Ile) n.822A>T | |
| 7 | g.152648685T>C | CA370197910 | XRCC2 | c.632A>G (p.Lys211Arg) c.800A>G (p.Lys267Arg) n.822A>G | |
| 7 | g.152648685T>G | CA370197911 | XRCC2 | c.632A>C (p.Lys211Thr) c.800A>C (p.Lys267Thr) n.822A>C | |
| 7 | g.152648686T>A | CA370197912 | XRCC2 | c.631A>T (p.Lys211Ter) c.799A>T (p.Lys267Ter) n.821A>T | |
| 7 | g.152648686T>C | CA370197913 | XRCC2 | c.631A>G (p.Lys211Glu) c.799A>G (p.Lys267Glu) n.821A>G | |
| 7 | g.152648686T>G | CA370197914 | XRCC2 | c.631A>C (p.Lys211Gln) c.799A>C (p.Lys267Gln) n.821A>C | |
| 7 | g.152648687T>A | CA370197915 | XRCC2 | c.630A>T (p.Lys210Asn) c.798A>T (p.Lys266Asn) n.820A>T | |
| 7 | g.152648687T>C | CA458895103 | XRCC2 | c.630A>G (p.Lys210=) c.798A>G (p.Lys266=) n.820A>G | |
| 7 | g.152648687T>G | CA370197916 | XRCC2 | c.630A>C (p.Lys210Asn) c.798A>C (p.Lys266Asn) n.820A>C | |
| 7 | g.152648688T>A | CA370197917 | XRCC2 | c.629A>T (p.Lys210Ile) c.797A>T (p.Lys266Ile) n.819A>T | |
| 7 | g.152648688T>C | CA370197918 | XRCC2 | c.629A>G (p.Lys210Arg) c.797A>G (p.Lys266Arg) n.819A>G | |
| 7 | g.152648688T>G | CA370197919 | XRCC2 | c.629A>C (p.Lys210Thr) c.797A>C (p.Lys266Thr) n.819A>C | |
| 7 | g.152648689T>A | CA370197920 | XRCC2 | c.628A>T (p.Lys210Ter) c.796A>T (p.Lys266Ter) n.818A>T | |
| 7 | g.152648689T>C | CA169486936 | XRCC2 | c.628A>G (p.Lys210Glu) c.796A>G (p.Lys266Glu) n.818A>G | dbSNP |
| 7 | g.152648689T>G | CA370197921 | XRCC2 | c.628A>C (p.Lys210Gln) c.796A>C (p.Lys266Gln) n.818A>C | |
| 7 | g.152648689T= | CA1753246546 | XRCC2 | c.628A= (p.Lys210=) c.796A= (p.Lys266=) n.818A= | |
| 7 | g.152648689_152648692delinsTTAA | CA1753246547 | XRCC2 | c.625_628delinsTTAA (p.Leu209=) c.793_796delinsTTAA (p.Leu265=) n.815_818delinsTTAA | |
| 7 | g.152648690T>A | CA370197922 | XRCC2 | c.627A>T (p.Leu209Phe) c.795A>T (p.Leu265Phe) n.817A>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648690T>C | CA458895200 | XRCC2 | c.627A>G (p.Leu209=) c.795A>G (p.Leu265=) n.817A>G | |
| 7 | g.152648690T>G | CA370197923 | XRCC2 | c.627A>C (p.Leu209Phe) c.795A>C (p.Leu265Phe) n.817A>C | |
| 7 | g.152648690T= | CA1753246548 | XRCC2 | c.627A= (p.Leu209=) c.795A= (p.Leu265=) n.817A= | |
| 7 | g.152648690_152648691delinsTA | CA1753246549 | XRCC2 | c.626_627delinsTA (p.Leu209=) c.794_795delinsTA (p.Leu265=) n.816_817delinsTA | |
| 7 | g.152648690_152648692del | CA835377062 | XRCC2 | c.625_627del (p.Leu209del) c.793_795del (p.Leu265del) n.815_817del | dbSNP |
| 7 | g.152648691A= | CA1753246557 | XRCC2 | c.626T= (p.Leu209=) c.794T= (p.Leu265=) n.816T= | |
| 7 | g.152648691A>C | CA370197924 | XRCC2 | c.626T>G (p.Leu209Ter) c.794T>G (p.Leu265Ter) n.816T>G | ClinVar dbSNP |
| 7 | g.152648691A>G | CA4582293 | XRCC2 | c.626T>C (p.Leu209Ser) c.794T>C (p.Leu265Ser) n.816T>C | ClinVar dbSNP ExAC gnomAD v2 |
| 7 | g.152648691A>T | CA4582294 | XRCC2 | c.626T>A (p.Leu209Ter) c.794T>A (p.Leu265Ter) n.816T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648693del | CA1139660349 | XRCC2 | c.626del (p.Leu209Ter) c.794del (p.Leu265Ter) n.816del | ClinVar dbSNP |
| 7 | g.152648692A= | CA1753246558 | XRCC2 | c.625T= (p.Leu209=) c.793T= (p.Leu265=) n.815T= | |
| 7 | g.152648692A>C | CA370197925 | XRCC2 | c.625T>G (p.Leu209Val) c.793T>G (p.Leu265Val) n.815T>G | |
| 7 | g.152648692A>G | CA458895201 | XRCC2 | c.625T>C (p.Leu209=) c.793T>C (p.Leu265=) n.815T>C | ClinVar |
| 7 | g.152648692A>T | CA370197926 | XRCC2 | c.625T>A (p.Leu209Ile) c.793T>A (p.Leu265Ile) n.815T>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648693A= | CA1753246559 | XRCC2 | c.624T= (p.Ser208=) c.792T= (p.Ser264=) n.814T= | |
| 7 | g.152648693A>C | CA370197927 | XRCC2 | c.624T>G (p.Ser208Arg) c.792T>G (p.Ser264Arg) n.814T>G | |
| 7 | g.152648693A>G | CA458895202 | XRCC2 | c.624T>C (p.Ser208=) c.792T>C (p.Ser264=) n.814T>C | ClinVar |
| 7 | g.152648693A>T | CA370197928 | XRCC2 | c.624T>A (p.Ser208Arg) c.792T>A (p.Ser264Arg) n.814T>A | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648694C>A | CA370197929 | XRCC2 | c.623G>T (p.Ser208Ile) c.791G>T (p.Ser264Ile) n.813G>T | gnomAD v4 |
| 7 | g.152648694C>G | CA370197930 | XRCC2 | c.623G>C (p.Ser208Thr) c.791G>C (p.Ser264Thr) n.813G>C | |
| 7 | g.152648694C>T | CA370197931 | XRCC2 | c.623G>A (p.Ser208Asn) c.791G>A (p.Ser264Asn) n.813G>A | ClinVar gnomAD v4 |
| 7 | g.152648694_152648696delinsCTG | CA1753246560 | XRCC2 | c.621_623delinsCAG (p.Asn207=) c.789_791delinsCAG (p.Asn263=) n.811_813delinsCAG | |
| 7 | g.152648695T>A | CA370197934 | XRCC2 | c.622A>T (p.Ser208Cys) c.790A>T (p.Ser264Cys) n.812A>T | |
| 7 | g.152648695T>C | CA370197932 | XRCC2 | c.622A>G (p.Ser208Gly) c.790A>G (p.Ser264Gly) n.812A>G | |
| 7 | g.152648695T>G | CA370197933 | XRCC2 | c.622A>C (p.Ser208Arg) c.790A>C (p.Ser264Arg) n.812A>C | gnomAD v4 |
| 7 | g.152648696_152648697del | CA16612057 | XRCC2 | c.621_622del (p.Asn207LysfsTer15) c.789_790del (p.Asn263LysfsTer15) n.811_812del | ClinVar dbSNP |
| 7 | g.152648696G>A | CA458895203 | XRCC2 | c.621C>T (p.Asn207=) c.789C>T (p.Asn263=) n.811C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648696G>C | CA370197935 | XRCC2 | c.621C>G (p.Asn207Lys) c.789C>G (p.Asn263Lys) n.811C>G | ClinVar dbSNP |
| 7 | g.152648696G= | CA1753246563 | XRCC2 | c.621C= (p.Asn207=) c.789C= (p.Asn263=) n.811C= | |
| 7 | g.152648696G>T | CA370197936 | XRCC2 | c.621C>A (p.Asn207Lys) c.789C>A (p.Asn263Lys) n.811C>A | |
| 7 | g.152648697T>A | CA370197937 | XRCC2 | c.620A>T (p.Asn207Ile) c.788A>T (p.Asn263Ile) n.810A>T | |
| 7 | g.152648697T>C | CA370197938 | XRCC2 | c.620A>G (p.Asn207Ser) c.788A>G (p.Asn263Ser) n.810A>G | |
| 7 | g.152648697T>G | CA370197939 | XRCC2 | c.620A>C (p.Asn207Thr) c.788A>C (p.Asn263Thr) n.810A>C | |
| 7 | g.152648697_152648700delinsTTAC | CA1753246564 | XRCC2 | c.617_620delinsGTAA (p.Ser206=) c.785_788delinsGTAA (p.Ser262=) n.807_810delinsGTAA | |
| 7 | g.152648698T>A | CA370197940 | XRCC2 | c.619A>T (p.Asn207Tyr) c.787A>T (p.Asn263Tyr) n.809A>T | |
| 7 | g.152648698T>C | CA370197941 | XRCC2 | c.619A>G (p.Asn207Asp) c.787A>G (p.Asn263Asp) n.809A>G | dbSNP |
| 7 | g.152648698T>G | CA370197942 | XRCC2 | c.619A>C (p.Asn207His) c.787A>C (p.Asn263His) n.809A>C | |
| 7 | g.152648698T= | CA1753246566 | XRCC2 | c.619A= (p.Asn207=) c.787A= (p.Asn263=) n.809A= | |
| 7 | g.152648699_152648701del | CA835377101 | XRCC2 | c.617_619del (p.Ser206del) c.785_787del (p.Ser262del) n.807_809del | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648698_152648709delinsTACTTTTTAAAC | CA1753246565 | XRCC2 | c.608_619delinsGTTTAAAAAGTA (p.Cys203=) c.776_787delinsGTTTAAAAAGTA (p.Cys259=) n.798_809delinsGTTTAAAAAGTA | |
| 7 | g.152648699A>C | CA370197943 | XRCC2 | c.618T>G (p.Ser206Arg) c.786T>G (p.Ser262Arg) n.808T>G | |
| 7 | g.152648699A>G | CA458895204 | XRCC2 | c.618T>C (p.Ser206=) c.786T>C (p.Ser262=) n.808T>C | |
| 7 | g.152648699A>T | CA370197944 | XRCC2 | c.618T>A (p.Ser206Arg) c.786T>A (p.Ser262Arg) n.808T>A | |
| 7 | g.152648699_152648709delinsGTTTA | CA288149 | XRCC2 | c.608_618delinsTAAAC (p.Cys203_Ser206delinsLeuAsn) c.776_786delinsTAAAC (p.Cys259_Ser262delinsLeuAsn) n.798_808delinsTAAAC | ClinVar dbSNP |
| 7 | g.152648700C>A | CA370197946 | XRCC2 | c.617G>T (p.Ser206Ile) c.785G>T (p.Ser262Ile) n.807G>T | |
| 7 | g.152648700C>G | CA370197947 | XRCC2 | c.617G>C (p.Ser206Thr) c.785G>C (p.Ser262Thr) n.807G>C | gnomAD v4 |
| 7 | g.152648700C>T | CA370197945 | XRCC2 | c.617G>A (p.Ser206Asn) c.785G>A (p.Ser262Asn) n.807G>A | |
| 7 | g.152648701T>A | CA370197948 | XRCC2 | c.616A>T (p.Ser206Cys) c.784A>T (p.Ser262Cys) n.806A>T | |
| 7 | g.152648701T>C | CA370197949 | XRCC2 | c.616A>G (p.Ser206Gly) c.784A>G (p.Ser262Gly) n.806A>G | ClinVar |
| 7 | g.152648701T>G | CA370197950 | XRCC2 | c.616A>C (p.Ser206Arg) c.784A>C (p.Ser262Arg) n.806A>C | |
| 7 | g.152648702T>A | CA370197951 | XRCC2 | c.615A>T (p.Lys205Asn) c.783A>T (p.Lys261Asn) n.805A>T | |
| 7 | g.152648702T>C | CA458895208 | XRCC2 | c.615A>G (p.Lys205=) c.783A>G (p.Lys261=) n.805A>G | |
| 7 | g.152648702T>G | CA370197952 | XRCC2 | c.615A>C (p.Lys205Asn) c.783A>C (p.Lys261Asn) n.805A>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648702T= | CA1753246569 | XRCC2 | c.615A= (p.Lys205=) c.783A= (p.Lys261=) n.805A= | |
| 7 | g.152648703T>A | CA370197953 | XRCC2 | c.614A>T (p.Lys205Ile) c.782A>T (p.Lys261Ile) n.804A>T | |
| 7 | g.152648703T>C | CA370197954 | XRCC2 | c.614A>G (p.Lys205Arg) c.782A>G (p.Lys261Arg) n.804A>G | |
| 7 | g.152648703T>G | CA4582295 | XRCC2 | c.614A>C (p.Lys205Thr) c.782A>C (p.Lys261Thr) n.804A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648703T= | CA1753246572 | XRCC2 | c.614A= (p.Lys205=) c.782A= (p.Lys261=) n.804A= | |
| 7 | g.152648704T>A | CA370197955 | XRCC2 | c.613A>T (p.Lys205Ter) c.781A>T (p.Lys261Ter) n.803A>T | |
| 7 | g.152648704T>C | CA370197956 | XRCC2 | c.613A>G (p.Lys205Glu) c.781A>G (p.Lys261Glu) n.803A>G | |
| 7 | g.152648704T>G | CA370197957 | XRCC2 | c.613A>C (p.Lys205Gln) c.781A>C (p.Lys261Gln) n.803A>C | |
| 7 | g.152648705T>A | CA370197958 | XRCC2 | c.612A>T (p.Leu204Phe) c.780A>T (p.Leu260Phe) n.802A>T | |
| 7 | g.152648705T>C | CA458895212 | XRCC2 | c.612A>G (p.Leu204=) c.780A>G (p.Leu260=) n.802A>G | |
| 7 | g.152648705T>G | CA370197959 | XRCC2 | c.612A>C (p.Leu204Phe) c.780A>C (p.Leu260Phe) n.802A>C | |
| 7 | g.152648706A>C | CA370197962 | XRCC2 | c.611T>G (p.Leu204Ter) c.779T>G (p.Leu260Ter) n.801T>G | |
| 7 | g.152648706A>G | CA370197961 | XRCC2 | c.611T>C (p.Leu204Ser) c.779T>C (p.Leu260Ser) n.801T>C | |
| 7 | g.152648706A>T | CA370197960 | XRCC2 | c.611T>A (p.Leu204Ter) c.779T>A (p.Leu260Ter) n.801T>A | |
| 7 | g.152648706_152648709delinsAAAC | CA1753246575 | XRCC2 | c.608_611delinsGTTT (p.Cys203=) c.776_779delinsGTTT (p.Cys259=) n.798_801delinsGTTT | |
| 7 | g.152648707A>C | CA370197963 | XRCC2 | c.610T>G (p.Leu204Val) c.778T>G (p.Leu260Val) n.800T>G | |
| 7 | g.152648707A>G | CA458895213 | XRCC2 | c.610T>C (p.Leu204=) c.778T>C (p.Leu260=) n.800T>C | |
| 7 | g.152648707A>T | CA370197964 | XRCC2 | c.610T>A (p.Leu204Ile) c.778T>A (p.Leu260Ile) n.800T>A | |
| 7 | g.152648710_152648712del | CA1108857602 | XRCC2 | c.608_610del (p.Cys203del) c.776_778del (p.Cys259del) n.798_800del | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648708A= | CA1753246579 | XRCC2 | c.609T= (p.Cys203=) c.777T= (p.Cys259=) n.799T= | |
| 7 | g.152648708A>C | CA370197965 | XRCC2 | c.609T>G (p.Cys203Trp) c.777T>G (p.Cys259Trp) n.799T>G | |
| 7 | g.152648708A>G | CA4582296 | XRCC2 | c.609T>C (p.Cys203=) c.777T>C (p.Cys259=) n.799T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648708A>T | CA370197966 | XRCC2 | c.609T>A (p.Cys203Ter) c.777T>A (p.Cys259Ter) n.799T>A | |
| 7 | g.152648709C>A | CA370197967 | XRCC2 | c.608G>T (p.Cys203Phe) c.776G>T (p.Cys259Phe) n.798G>T | |
| 7 | g.152648709C>G | CA370197968 | XRCC2 | c.608G>C (p.Cys203Ser) c.776G>C (p.Cys259Ser) n.798G>C | |
| 7 | g.152648709C>T | CA370197969 | XRCC2 | c.608G>A (p.Cys203Tyr) c.776G>A (p.Cys259Tyr) n.798G>A | ClinVar dbSNP gnomAD v4 |
| 7 | g.152648710A>C | CA370197970 | XRCC2 | c.607T>G (p.Cys203Gly) c.775T>G (p.Cys259Gly) n.797T>G | |
| 7 | g.152648710A>G | CA370197971 | XRCC2 | c.607T>C (p.Cys203Arg) c.775T>C (p.Cys259Arg) n.797T>C | |
| 7 | g.152648710A>T | CA370197972 | XRCC2 | c.607T>A (p.Cys203Ser) c.775T>A (p.Cys259Ser) n.797T>A | |
| 7 | g.152648711A>C | CA458895218 | XRCC2 | c.606T>G (p.Arg202=) c.774T>G (p.Arg258=) n.796T>G | |
| 7 | g.152648711A>G | CA458895217 | XRCC2 | c.606T>C (p.Arg202=) c.774T>C (p.Arg258=) n.796T>C | |
| 7 | g.152648711A>T | CA458895216 | XRCC2 | c.606T>A (p.Arg202=) c.774T>A (p.Arg258=) n.796T>A | |
| 7 | g.152648712C>A | CA370197973 | XRCC2 | c.605G>T (p.Arg202Leu) c.773G>T (p.Arg258Leu) n.795G>T | |
| 7 | g.152648712C= | CA1753246582 | XRCC2 | c.605G= (p.Arg202=) c.773G= (p.Arg258=) n.795G= | |
| 7 | g.152648712C>G | CA370197974 | XRCC2 | c.605G>C (p.Arg202Pro) c.773G>C (p.Arg258Pro) n.795G>C | |
| 7 | g.152648712C>T | CA288147 | XRCC2 | c.605G>A (p.Arg202His) c.773G>A (p.Arg258His) n.795G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648713G>A | CA4582297 | XRCC2 | c.604C>T (p.Arg202Cys) c.772C>T (p.Arg258Cys) n.794C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648713G>C | CA370197976 | XRCC2 | c.604C>G (p.Arg202Gly) c.772C>G (p.Arg258Gly) n.794C>G | |
| 7 | g.152648713G= | CA1753246586 | XRCC2 | c.604C= (p.Arg202=) c.772C= (p.Arg258=) n.794C= | |
| 7 | g.152648713G>T | CA370197975 | XRCC2 | c.604C>A (p.Arg202Ser) c.772C>A (p.Arg258Ser) n.794C>A | |
| 7 | g.152648714T>A | CA458895219 | XRCC2 | c.603A>T (p.Ser201=) c.771A>T (p.Ser257=) n.793A>T | |
| 7 | g.152648714T>C | CA458895220 | XRCC2 | c.603A>G (p.Ser201=) c.771A>G (p.Ser257=) n.793A>G | |
| 7 | g.152648714T>G | CA458895222 | XRCC2 | c.603A>C (p.Ser201=) c.771A>C (p.Ser257=) n.793A>C | |
| 7 | g.152648715G>A | CA300485 | XRCC2 | c.602C>T (p.Ser201Leu) c.770C>T (p.Ser257Leu) n.792C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.152648715G>C | CA370197977 | XRCC2 | c.602C>G (p.Ser201Ter) c.770C>G (p.Ser257Ter) n.792C>G | |
| 7 | g.152648715G= | CA1753246592 | XRCC2 | c.602C= (p.Ser201=) c.770C= (p.Ser257=) n.792C= | |
| 7 | g.152648715G>T | CA370197978 | XRCC2 | c.602C>A (p.Ser201Ter) c.770C>A (p.Ser257Ter) n.792C>A | dbSNP gnomAD v4 |
| 7 | g.152648716A>C | CA370197979 | XRCC2 | c.601T>G (p.Ser201Ala) c.769T>G (p.Ser257Ala) n.791T>G | |
| 7 | g.152648716A>G | CA370197980 | XRCC2 | c.601T>C (p.Ser201Pro) c.769T>C (p.Ser257Pro) n.791T>C | |
| 7 | g.152648716A>T | CA370197981 | XRCC2 | c.601T>A (p.Ser201Thr) c.769T>A (p.Ser257Thr) n.791T>A | |
| 7 | g.152648717A>C | CA458895223 | XRCC2 | c.600T>G (p.Val200=) c.768T>G (p.Val256=) n.790T>G | |
| 7 | g.152648717A>G | CA458895224 | XRCC2 | c.600T>C (p.Val200=) c.768T>C (p.Val256=) n.790T>C | |
| 7 | g.152648717A>T | CA458895225 | XRCC2 | c.600T>A (p.Val200=) c.768T>A (p.Val256=) n.790T>A | |
| 7 | g.152648717_152648718delinsAA | CA1753246597 | XRCC2 | c.599_600delinsTT (p.Val200=) c.767_768delinsTT (p.Val256=) n.789_790delinsTT | |
| 7 | g.152648717_152648718delinsCT | CA16618425 | XRCC2 | c.599_600delinsAG (p.Val200Glu) c.767_768delinsAG (p.Val256Glu) n.789_790delinsAG | ClinVar dbSNP |
| 7 | g.152648718A>C | CA370197984 | XRCC2 | c.599T>G (p.Val200Gly) c.767T>G (p.Val256Gly) n.789T>G | COSMIC |
| 7 | g.152648718A>G | CA370197982 | XRCC2 | c.599T>C (p.Val200Ala) c.767T>C (p.Val256Ala) n.789T>C | |
| 7 | g.152648718A>T | CA370197983 | XRCC2 | c.599T>A (p.Val200Asp) c.767T>A (p.Val256Asp) n.789T>A | |
| 7 | g.152648719C>A | CA370197985 | XRCC2 | c.598G>T (p.Val200Phe) c.766G>T (p.Val256Phe) n.788G>T | |
| 7 | g.152648719C>G | CA370197986 | XRCC2 | c.598G>C (p.Val200Leu) c.766G>C (p.Val256Leu) n.788G>C | |
| 7 | g.152648719C>T | CA370197987 | XRCC2 | c.598G>A (p.Val200Ile) c.766G>A (p.Val256Ile) n.788G>A | dbSNP |
| 7 | g.152648720T>A | CA370197988 | XRCC2 | c.597A>T (p.Leu199Phe) c.765A>T (p.Leu255Phe) n.787A>T | |
| 7 | g.152648720T>C | CA458895228 | XRCC2 | c.597A>G (p.Leu199=) c.765A>G (p.Leu255=) n.787A>G | |
| 7 | g.152648720T>G | CA370197989 | XRCC2 | c.597A>C (p.Leu199Phe) c.765A>C (p.Leu255Phe) n.787A>C | |
| 7 | g.152648721A= | CA1753246604 | XRCC2 | c.596T= (p.Leu199=) c.764T= (p.Leu255=) n.786T= | |
| 7 | g.152648721A>C | CA4582298 | XRCC2 | c.596T>G (p.Leu199Ter) c.764T>G (p.Leu255Ter) n.786T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.152648721A>G | CA370197991 | XRCC2 | c.596T>C (p.Leu199Ser) c.764T>C (p.Leu255Ser) n.786T>C | |
| 7 | g.152648721A>T | CA370197990 | XRCC2 | c.596T>A (p.Leu199Ter) c.764T>A (p.Leu255Ter) n.786T>A | |
| 7 | g.152648722A>C | CA370197992 | XRCC2 | c.595T>G (p.Leu199Val) c.763T>G (p.Leu255Val) n.785T>G | |
| 7 | g.152648722A>G | CA458895229 | XRCC2 | c.595T>C (p.Leu199=) c.763T>C (p.Leu255=) n.785T>C | |
| 7 | g.152648722A>T | CA370197993 | XRCC2 | c.595T>A (p.Leu199Ile) c.763T>A (p.Leu255Ile) n.785T>A | |
| 7 | g.152648723T>A | CA458895230 | XRCC2 | c.594A>T (p.Ser198=) c.762A>T (p.Ser254=) n.784A>T | |
| 7 | g.152648723T>C | CA458895231 | XRCC2 | c.594A>G (p.Ser198=) c.762A>G (p.Ser254=) n.784A>G | |
| 7 | g.152648723T>G | CA458895232 | XRCC2 | c.594A>C (p.Ser198=) c.762A>C (p.Ser254=) n.784A>C | |
| 7 | g.152648724G>A | CA370197994 | XRCC2 | c.593C>T (p.Ser198Leu) c.761C>T (p.Ser254Leu) n.783C>T | dbSNP |
| 7 | g.152648724G>C | CA370197995 | XRCC2 | c.593C>G (p.Ser198Ter) c.761C>G (p.Ser254Ter) n.783C>G | |
| 7 | g.152648724G= | CA1753246607 | XRCC2 | c.593C= (p.Ser198=) c.761C= (p.Ser254=) n.783C= | |
| 7 | g.152648724G>T | CA370197996 | XRCC2 | c.593C>A (p.Ser198Ter) c.761C>A (p.Ser254Ter) n.783C>A | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.152648725A>C | CA370197997 | XRCC2 | c.592T>G (p.Ser198Ala) c.760T>G (p.Ser254Ala) n.782T>G | |
| 7 | g.152648725A>G | CA370197998 | XRCC2 | c.592T>C (p.Ser198Pro) c.760T>C (p.Ser254Pro) n.782T>C | |
| 7 | g.152648725A>T | CA370197999 | XRCC2 | c.592T>A (p.Ser198Thr) c.760T>A (p.Ser254Thr) n.782T>A | |
| 7 | g.152648726A>C | CA370198000 | XRCC2 | c.591T>G (p.Phe197Leu) c.759T>G (p.Phe253Leu) n.781T>G | |
| 7 | g.152648726A>G | CA458895233 | XRCC2 | c.591T>C (p.Phe197=) c.759T>C (p.Phe253=) n.781T>C | |
| 7 | g.152648726A>T | CA370198001 | XRCC2 | c.591T>A (p.Phe197Leu) c.759T>A (p.Phe253Leu) n.781T>A | ClinVar |
| 7 | g.152648727A>C | CA370198004 | XRCC2 | c.590T>G (p.Phe197Cys) c.758T>G (p.Phe253Cys) n.780T>G | |
| 7 | g.152648727A>G | CA370198003 | XRCC2 | c.590T>C (p.Phe197Ser) c.758T>C (p.Phe253Ser) n.780T>C | |
| 7 | g.152648727A>T | CA370198002 | XRCC2 | c.590T>A (p.Phe197Tyr) c.758T>A (p.Phe253Tyr) n.780T>A | |
| 7 | g.152648727_152648729del | CA2580077736 | XRCC2 | c.588_590del (p.Gln196_Phe197delinsHis) c.756_758del (p.Gln252_Phe253delinsHis) n.778_780del | ClinVar |
| 7 | g.152648728A>C | CA370198005 | XRCC2 | c.589T>G (p.Phe197Val) c.757T>G (p.Phe253Val) n.779T>G | |
| 7 | g.152648728A>G | CA370198007 | XRCC2 | c.589T>C (p.Phe197Leu) c.757T>C (p.Phe253Leu) n.779T>C | |
| 7 | g.152648728A>T | CA370198006 | XRCC2 | c.589T>A (p.Phe197Ile) c.757T>A (p.Phe253Ile) n.779T>A | |
| 7 | g.152648729T>A | CA370198008 | XRCC2 | c.588A>T (p.Gln196His) c.756A>T (p.Gln252His) n.778A>T | |
| 7 | g.152648729T>C | CA458895234 | XRCC2 | c.588A>G (p.Gln196=) c.756A>G (p.Gln252=) n.778A>G | ClinVar dbSNP |
| 7 | g.152648729T>G | CA370198009 | XRCC2 | c.588A>C (p.Gln196His) c.756A>C (p.Gln252His) n.778A>C | |
| 7 | g.152648729T= | CA1753246612 | XRCC2 | c.588A= (p.Gln196=) c.756A= (p.Gln252=) n.778A= | |
| 7 | g.152648730T>A | CA370198010 | XRCC2 | c.587A>T (p.Gln196Leu) c.755A>T (p.Gln252Leu) n.777A>T | |
| 7 | g.152648730T>C | CA370198012 | XRCC2 | c.587A>G (p.Gln196Arg) c.755A>G (p.Gln252Arg) n.777A>G | |
| 7 | g.152648730T>G | CA370198011 | XRCC2 | c.587A>C (p.Gln196Pro) c.755A>C (p.Gln252Pro) n.777A>C |