Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.152648612_152648662delCA2685735740XRCC2c.656_*31del (n.[c.656_*31del;Ser219ThrfsTer?])
c.824_*31del (n.[c.824_*31del;Ser275ThrfsTer?])
n.846_896del
 gnomAD v4
7g.152648647_152648656delCA2580077731XRCC2c.666_675del (p.Glu222AspfsTer16)
c.834_843del (p.Glu278AspfsTer16)
n.856_865del
 ClinVar
7g.152648655_152648656delinsACCA1753246485XRCC2c.661_662delinsGT (p.Val221=)
c.829_830delinsGT (p.Val277=)
n.851_852delinsGT
7g.152648656C>ACA370197846XRCC2c.661G>T (p.Val221Phe)
c.829G>T (p.Val277Phe)
n.851G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648656C=CA1753246487XRCC2c.661G= (p.Val221=)
c.829G= (p.Val277=)
n.851G=
7g.152648656C>GCA370197847XRCC2c.661G>C (p.Val221Leu)
c.829G>C (p.Val277Leu)
n.851G>C
7g.152648656C>TCA4582286XRCC2c.661G>A (p.Val221Ile)
c.829G>A (p.Val277Ile)
n.851G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648659delCA4582285XRCC2c.661del (p.Val221LeufsTer20)
c.829del (p.Val277LeufsTer20)
n.851del
 dbSNP ExAC gnomAD v2
7g.152648657C>ACA458895063XRCC2c.660G>T (p.Gly220=)
c.828G>T (p.Gly276=)
n.850G>T
 dbSNP gnomAD v4
7g.152648657C=CA1753246491XRCC2c.660G= (p.Gly220=)
c.828G= (p.Gly276=)
n.850G=
7g.152648657C>GCA458895061XRCC2c.660G>C (p.Gly220=)
c.828G>C (p.Gly276=)
n.850G>C
 ClinVar gnomAD v4
7g.152648657C>TCA458895059XRCC2c.660G>A (p.Gly220=)
c.828G>A (p.Gly276=)
n.850G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648658C>ACA370197848XRCC2c.659G>T (p.Gly220Val)
c.827G>T (p.Gly276Val)
n.849G>T
 dbSNP gnomAD v4
7g.152648658C>GCA370197849XRCC2c.659G>C (p.Gly220Ala)
c.827G>C (p.Gly276Ala)
n.849G>C
 COSMIC
7g.152648658C>TCA370197850XRCC2c.659G>A (p.Gly220Glu)
c.827G>A (p.Gly276Glu)
n.849G>A
 ClinVar
7g.152648659C>ACA370197852XRCC2c.658G>T (p.Gly220Trp)
c.826G>T (p.Gly276Trp)
n.848G>T
7g.152648659C=CA1753246495XRCC2c.658G= (p.Gly220=)
c.826G= (p.Gly276=)
n.848G=
7g.152648659C>GCA370197851XRCC2c.658G>C (p.Gly220Arg)
c.826G>C (p.Gly276Arg)
n.848G>C
7g.152648659C>TCA300481XRCC2c.658G>A (p.Gly220Arg)
c.826G>A (p.Gly276Arg)
n.848G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648660_152648661delCA2685735756XRCC2c.657_658del (p.Ser219ArgfsTer3)
c.825_826del (p.Ser275ArgfsTer3)
n.847_848del
 gnomAD v4
7g.152648660A=CA1753246500XRCC2c.657T= (p.Ser219=)
c.825T= (p.Ser275=)
n.847T=
7g.152648660A>CCA4582288XRCC2c.657T>G (p.Ser219Arg)
c.825T>G (p.Ser275Arg)
n.847T>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648660A>GCA4582287XRCC2c.657T>C (p.Ser219=)
c.825T>C (p.Ser275=)
n.847T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648660A>TCA370197853XRCC2c.657T>A (p.Ser219Arg)
c.825T>A (p.Ser275Arg)
n.847T>A
7g.152648661C>ACA370197854XRCC2c.656G>T (p.Ser219Ile)
c.824G>T (p.Ser275Ile)
n.846G>T
7g.152648661C>GCA370197855XRCC2c.656G>C (p.Ser219Thr)
c.824G>C (p.Ser275Thr)
n.846G>C
7g.152648661C>TCA370197856XRCC2c.656G>A (p.Ser219Asn)
c.824G>A (p.Ser275Asn)
n.846G>A
7g.152648662T>ACA370197857XRCC2c.655A>T (p.Ser219Cys)
c.823A>T (p.Ser275Cys)
n.845A>T
7g.152648662T>CCA370197858XRCC2c.655A>G (p.Ser219Gly)
c.823A>G (p.Ser275Gly)
n.845A>G
 dbSNP gnomAD v3 gnomAD v4
7g.152648662T>GCA370197859XRCC2c.655A>C (p.Ser219Arg)
c.823A>C (p.Ser275Arg)
n.845A>C
7g.152648662T=CA1753246503XRCC2c.655A= (p.Ser219=)
c.823A= (p.Ser275=)
n.845A=
7g.152648662_152648663insGGCCA2685735757XRCC2c.654_655insGCC (p.Glu218_Ser219insAla)
c.822_823insGCC (p.Glu274_Ser275insAla)
n.844_845insGCC
 gnomAD v4
7g.152648662_152648663insGGCTGGGCGCGGTGGCCA2685735758XRCC2c.654_655insGCCACCGCGCCCAGCC (p.Ser219AlafsTer9)
c.822_823insGCCACCGCGCCCAGCC (p.Ser275AlafsTer9)
n.844_845insGCCACCGCGCCCAGCC
 gnomAD v4
7g.152648663T>ACA370197860XRCC2c.654A>T (p.Glu218Asp)
c.822A>T (p.Glu274Asp)
n.844A>T
7g.152648663T>CCA458895066XRCC2c.654A>G (p.Glu218=)
c.822A>G (p.Glu274=)
n.844A>G
7g.152648663T>GCA4582289XRCC2c.654A>C (p.Glu218Asp)
c.822A>C (p.Glu274Asp)
n.844A>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648663T=CA1753246504XRCC2c.654A= (p.Glu218=)
c.822A= (p.Glu274=)
n.844A=
7g.152648663_152648664insGGGCGCGGTGGCCA2685735759XRCC2c.653_654insGCCACCGCGCCC (p.Glu218_Ser219insProProArgPro)
c.821_822insGCCACCGCGCCC (p.Glu274_Ser275insProProArgPro)
n.843_844insGCCACCGCGCCC
 gnomAD v4
7g.152648664T>ACA370197861XRCC2c.653A>T (p.Glu218Val)
c.821A>T (p.Glu274Val)
n.843A>T
7g.152648664T>CCA16618423XRCC2c.653A>G (p.Glu218Gly)
c.821A>G (p.Glu274Gly)
n.843A>G
 ClinVar dbSNP gnomAD v4
7g.152648664T>GCA370197862XRCC2c.653A>C (p.Glu218Ala)
c.821A>C (p.Glu274Ala)
n.843A>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648664T=CA1753246508XRCC2c.653A= (p.Glu218=)
c.821A= (p.Glu274=)
n.843A=
7g.152648666_152648667dupCA658823261XRCC2c.652_653dup (p.Ser219LysfsTer23)
c.820_821dup (p.Ser275LysfsTer23)
n.842_843dup
 ClinVar dbSNP gnomAD v4
7g.152648665C>ACA370197864XRCC2c.652G>T (p.Glu218Ter)
c.820G>T (p.Glu274Ter)
n.842G>T
7g.152648665C>GCA370197865XRCC2c.652G>C (p.Glu218Gln)
c.820G>C (p.Glu274Gln)
n.842G>C
7g.152648665C>TCA370197863XRCC2c.652G>A (p.Glu218Lys)
c.820G>A (p.Glu274Lys)
n.842G>A
 dbSNP
7g.152648665_152648666insACGCCTGTAACA2685735760XRCC2c.651_652insTTACAGGCGT (p.Glu218LeufsTer4)
c.819_820insTTACAGGCGT (p.Glu274LeufsTer4)
n.841_842insTTACAGGCGT
 gnomAD v4
7g.152648666T>ACA458895071XRCC2c.651A>T (p.Gly217=)
c.819A>T (p.Gly273=)
n.841A>T
7g.152648666T>CCA458895073XRCC2c.651A>G (p.Gly217=)
c.819A>G (p.Gly273=)
n.841A>G
7g.152648666T>GCA458895072XRCC2c.651A>C (p.Gly217=)
c.819A>C (p.Gly273=)
n.841A>C
7g.152648666T=CA1753246509XRCC2c.651A= (p.Gly217=)
c.819A= (p.Gly273=)
n.841A=
7g.152648666_152648667insGGGCGCA2685735761XRCC2c.650_651insCGCCC (p.Glu218AlafsTer25)
c.818_819insCGCCC (p.Glu274AlafsTer25)
n.840_841insCGCCC
 gnomAD v4
7g.152648666_152648667insGGGCGCGGTGGCA2685735762XRCC2c.650_651insCCACCGCGCCC (p.Glu218HisfsTer27)
c.818_819insCCACCGCGCCC (p.Glu274HisfsTer27)
n.840_841insCCACCGCGCCC
 gnomAD v4
7g.152648666_152648667insGGGCGCGGTGGCTCACGCA2685735763XRCC2c.650_651insCGTGAGCCACCGCGCCC (p.Glu218ValfsTer29)
c.818_819insCGTGAGCCACCGCGCCC (p.Glu274ValfsTer29)
n.840_841insCGTGAGCCACCGCGCCC
 gnomAD v4
7g.152648666_152648667insGGGCGCGGTGGCTCACGCCTGTAATCCA2685735764XRCC2c.650_651insGATTACAGGCGTGAGCCACCGCGCCC (p.Glu218IlefsTer32)
c.818_819insGATTACAGGCGTGAGCCACCGCGCCC (p.Glu274IlefsTer32)
n.840_841insGATTACAGGCGTGAGCCACCGCGCCC
 gnomAD v4
7g.152648666_152648667insGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCA579080835XRCC2c.650_651insCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCC (p.Gly217_Glu218insLeuGlyLeuProLysCysTrpAspTyrArgArgGluProProArgPro)
c.818_819insCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCC (p.Gly273_Glu274insLeuGlyLeuProLysCysTrpAspTyrArgArgGluProProArgPro)
n.840_841insCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCC
 dbSNP gnomAD v2
7g.152648667C>ACA370197866XRCC2c.650G>T (p.Gly217Val)
c.818G>T (p.Gly273Val)
n.840G>T
7g.152648667C>GCA370197867XRCC2c.650G>C (p.Gly217Ala)
c.818G>C (p.Gly273Ala)
n.840G>C
 COSMIC
7g.152648667C>TCA370197868XRCC2c.650G>A (p.Gly217Glu)
c.818G>A (p.Gly273Glu)
n.840G>A
 ClinVar dbSNP
7g.152648668C>ACA370197869XRCC2c.649G>T (p.Gly217Ter)
c.817G>T (p.Gly273Ter)
n.839G>T
7g.152648668C=CA1753246517XRCC2c.649G= (p.Gly217=)
c.817G= (p.Gly273=)
n.839G=
7g.152648668C>GCA370197870XRCC2c.649G>C (p.Gly217Arg)
c.817G>C (p.Gly273Arg)
n.839G>C
7g.152648668C>TCA370197871XRCC2c.649G>A (p.Gly217Arg)
c.817G>A (p.Gly273Arg)
n.839G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648668_152648671delinsCAATCA1753246516XRCC2c.646_649delinsATTG (p.Ile216=)
c.814_817delinsATTG (p.Ile272=)
n.836_839delinsATTG
7g.152648669A>CCA370197872XRCC2c.648T>G (p.Ile216Met)
c.816T>G (p.Ile272Met)
n.838T>G
7g.152648669A>GCA458895077XRCC2c.648T>C (p.Ile216=)
c.816T>C (p.Ile272=)
n.838T>C
7g.152648669A>TCA458895079XRCC2c.648T>A (p.Ile216=)
c.816T>A (p.Ile272=)
n.838T>A
 gnomAD v4
7g.152648674_152648676delCA1108857565XRCC2c.646_648del (p.Ile216del)
c.814_816del (p.Ile272del)
n.836_838del
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648670A>CCA370197873XRCC2c.647T>G (p.Ile216Ser)
c.815T>G (p.Ile272Ser)
n.837T>G
7g.152648670A>GCA370197875XRCC2c.647T>C (p.Ile216Thr)
c.815T>C (p.Ile272Thr)
n.837T>C
 gnomAD v4
7g.152648670A>TCA370197874XRCC2c.647T>A (p.Ile216Asn)
c.815T>A (p.Ile272Asn)
n.837T>A
7g.152648671T>ACA370197876XRCC2c.646A>T (p.Ile216Phe)
c.814A>T (p.Ile272Phe)
n.836A>T
 dbSNP
7g.152648671T>CCA370197877XRCC2c.646A>G (p.Ile216Val)
c.814A>G (p.Ile272Val)
n.836A>G
 gnomAD v4
7g.152648671T>GCA370197878XRCC2c.646A>C (p.Ile216Leu)
c.814A>C (p.Ile272Leu)
n.836A>C
7g.152648672A>CCA370197879XRCC2c.645T>G (p.Ile215Met)
c.813T>G (p.Ile271Met)
n.835T>G
7g.152648672A>GCA458895084XRCC2c.645T>C (p.Ile215=)
c.813T>C (p.Ile271=)
n.835T>C
7g.152648672A>TCA458895083XRCC2c.645T>A (p.Ile215=)
c.813T>A (p.Ile271=)
n.835T>A
7g.152648673A>CCA370197880XRCC2c.644T>G (p.Ile215Ser)
c.812T>G (p.Ile271Ser)
n.834T>G
7g.152648673A>GCA370197882XRCC2c.644T>C (p.Ile215Thr)
c.812T>C (p.Ile271Thr)
n.834T>C
7g.152648673A>TCA370197881XRCC2c.644T>A (p.Ile215Asn)
c.812T>A (p.Ile271Asn)
n.834T>A
7g.152648674T>ACA370197883XRCC2c.643A>T (p.Ile215Phe)
c.811A>T (p.Ile271Phe)
n.833A>T
7g.152648674T>CCA288153XRCC2c.643A>G (p.Ile215Val)
c.811A>G (p.Ile271Val)
n.833A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648674T>GCA370197884XRCC2c.643A>C (p.Ile215Leu)
c.811A>C (p.Ile271Leu)
n.833A>C
7g.152648674T=CA1753246523XRCC2c.643A= (p.Ile215=)
c.811A= (p.Ile271=)
n.833A=
7g.152648674_152648677delinsTAAACA1753246524XRCC2c.640_643delinsTTTA (p.Phe214=)
c.808_811delinsTTTA (p.Phe270=)
n.830_833delinsTTTA
7g.152648675A>CCA370197885XRCC2c.642T>G (p.Phe214Leu)
c.810T>G (p.Phe270Leu)
n.832T>G
7g.152648675A>GCA458895088XRCC2c.642T>C (p.Phe214=)
c.810T>C (p.Phe270=)
n.832T>C
7g.152648675A>TCA370197886XRCC2c.642T>A (p.Phe214Leu)
c.810T>A (p.Phe270Leu)
n.832T>A
7g.152648681dupCA16618424XRCC2c.642dup (p.Ile215TyrfsTer8)
c.810dup (p.Ile271TyrfsTer8)
n.832dup
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648681delCA2685735765XRCC2c.642del (p.Phe214LeufsTer27)
c.810del (p.Phe270LeufsTer27)
n.832del
 dbSNP gnomAD v4
7g.152648679_152648681delCA300488XRCC2c.640_642del (p.Phe214del)
c.808_810del (p.Phe270del)
n.830_832del
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648676A>CCA370197887XRCC2c.641T>G (p.Phe214Cys)
c.809T>G (p.Phe270Cys)
n.831T>G
 ClinVar
7g.152648676A>GCA370197888XRCC2c.641T>C (p.Phe214Ser)
c.809T>C (p.Phe270Ser)
n.831T>C
7g.152648676A>TCA370197889XRCC2c.641T>A (p.Phe214Tyr)
c.809T>A (p.Phe270Tyr)
n.831T>A
7g.152648677A=CA1753246532XRCC2c.640T= (p.Phe214=)
c.808T= (p.Phe270=)
n.830T=
7g.152648677A>CCA288151XRCC2c.640T>G (p.Phe214Val)
c.808T>G (p.Phe270Val)
n.830T>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648677A>GCA370197891XRCC2c.640T>C (p.Phe214Leu)
c.808T>C (p.Phe270Leu)
n.830T>C
7g.152648677A>TCA370197890XRCC2c.640T>A (p.Phe214Ile)
c.808T>A (p.Phe270Ile)
n.830T>A
7g.152648678A>CCA370197892XRCC2c.639T>G (p.Phe213Leu)
c.807T>G (p.Phe269Leu)
n.829T>G
 ClinVar
7g.152648678A>GCA458895090XRCC2c.639T>C (p.Phe213=)
c.807T>C (p.Phe269=)
n.829T>C
7g.152648678A>TCA370197893XRCC2c.639T>A (p.Phe213Leu)
c.807T>A (p.Phe269Leu)
n.829T>A
7g.152648679A>CCA370197894XRCC2c.638T>G (p.Phe213Cys)
c.806T>G (p.Phe269Cys)
n.828T>G
7g.152648679A>GCA370197895XRCC2c.638T>C (p.Phe213Ser)
c.806T>C (p.Phe269Ser)
n.828T>C
7g.152648679A>TCA370197896XRCC2c.638T>A (p.Phe213Tyr)
c.806T>A (p.Phe269Tyr)
n.828T>A
7g.152648679_152648731delCA2685735766XRCC2c.586_638del (p.Gln196PhefsTer9)
c.754_806del (p.Gln252PhefsTer9)
n.776_828del
 gnomAD v4
7g.152648680A=CA1753246534XRCC2c.637T= (p.Phe213=)
c.805T= (p.Phe269=)
n.827T=
7g.152648680A>CCA370197897XRCC2c.637T>G (p.Phe213Val)
c.805T>G (p.Phe269Val)
n.827T>G
7g.152648680A>GCA370197898XRCC2c.637T>C (p.Phe213Leu)
c.805T>C (p.Phe269Leu)
n.827T>C
 ClinVar
7g.152648680A>TCA4582290XRCC2c.637T>A (p.Phe213Ile)
c.805T>A (p.Phe269Ile)
n.827T>A
 ClinVar dbSNP ExAC gnomAD v2
7g.152648681A>CCA370197899XRCC2c.636T>G (p.His212Gln)
c.804T>G (p.His268Gln)
n.826T>G
7g.152648681A>GCA458895093XRCC2c.636T>C (p.His212=)
c.804T>C (p.His268=)
n.826T>C
7g.152648681A>TCA370197900XRCC2c.636T>A (p.His212Gln)
c.804T>A (p.His268Gln)
n.826T>A
 ClinVar
7g.152648681_152648682delinsATCA1753246537XRCC2c.635_636delinsAT (p.His212=)
c.803_804delinsAT (p.His268=)
n.825_826delinsAT
7g.152648681_152648684delinsATGTCA1753246538XRCC2c.633_636delinsACAT (p.Lys211=)
c.801_804delinsACAT (p.Lys267=)
n.823_826delinsACAT
7g.152648682delCA4582291XRCC2c.635del (p.His212LeufsTer29)
c.803del (p.His268LeufsTer29)
n.825del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648682T>ACA370197901XRCC2c.635A>T (p.His212Leu)
c.803A>T (p.His268Leu)
n.825A>T
7g.152648682T>CCA370197903XRCC2c.635A>G (p.His212Arg)
c.803A>G (p.His268Arg)
n.825A>G
7g.152648682T>GCA370197902XRCC2c.635A>C (p.His212Pro)
c.803A>C (p.His268Pro)
n.825A>C
7g.152648683_152648685delCA915945586XRCC2c.633_635del (p.Lys211_His212delinsAsn)
c.801_803del (p.Lys267_His268delinsAsn)
n.823_825del
 ClinVar dbSNP
7g.152648683G>ACA370197904XRCC2c.634C>T (p.His212Tyr)
c.802C>T (p.His268Tyr)
n.824C>T
 ClinVar
7g.152648683G>CCA370197905XRCC2c.634C>G (p.His212Asp)
c.802C>G (p.His268Asp)
n.824C>G
7g.152648683G>TCA370197906XRCC2c.634C>A (p.His212Asn)
c.802C>A (p.His268Asn)
n.824C>A
7g.152648683_152648684delinsGTCA1753246542XRCC2c.633_634delinsAC (p.Lys211=)
c.801_802delinsAC (p.Lys267=)
n.823_824delinsAC
7g.152648684T>ACA370197908XRCC2c.633A>T (p.Lys211Asn)
c.801A>T (p.Lys267Asn)
n.823A>T
7g.152648684T>CCA458895100XRCC2c.633A>G (p.Lys211=)
c.801A>G (p.Lys267=)
n.823A>G
 ClinVar dbSNP
7g.152648684T>GCA370197907XRCC2c.633A>C (p.Lys211Asn)
c.801A>C (p.Lys267Asn)
n.823A>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648684T=CA1753246544XRCC2c.633A= (p.Lys211=)
c.801A= (p.Lys267=)
n.823A=
7g.152648690dupCA4582292XRCC2c.633dup (p.His212ThrfsTer11)
c.801dup (p.His268ThrfsTer11)
n.823dup
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648690delCA458895101XRCC2c.633del (p.Lys211AsnfsTer30)
c.801del (p.Lys267AsnfsTer30)
n.823del
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.152648685T>ACA370197909XRCC2c.632A>T (p.Lys211Ile)
c.800A>T (p.Lys267Ile)
n.822A>T
7g.152648685T>CCA370197910XRCC2c.632A>G (p.Lys211Arg)
c.800A>G (p.Lys267Arg)
n.822A>G
7g.152648685T>GCA370197911XRCC2c.632A>C (p.Lys211Thr)
c.800A>C (p.Lys267Thr)
n.822A>C
7g.152648686T>ACA370197912XRCC2c.631A>T (p.Lys211Ter)
c.799A>T (p.Lys267Ter)
n.821A>T
7g.152648686T>CCA370197913XRCC2c.631A>G (p.Lys211Glu)
c.799A>G (p.Lys267Glu)
n.821A>G
7g.152648686T>GCA370197914XRCC2c.631A>C (p.Lys211Gln)
c.799A>C (p.Lys267Gln)
n.821A>C
7g.152648687T>ACA370197915XRCC2c.630A>T (p.Lys210Asn)
c.798A>T (p.Lys266Asn)
n.820A>T
7g.152648687T>CCA458895103XRCC2c.630A>G (p.Lys210=)
c.798A>G (p.Lys266=)
n.820A>G
7g.152648687T>GCA370197916XRCC2c.630A>C (p.Lys210Asn)
c.798A>C (p.Lys266Asn)
n.820A>C
7g.152648688T>ACA370197917XRCC2c.629A>T (p.Lys210Ile)
c.797A>T (p.Lys266Ile)
n.819A>T
7g.152648688T>CCA370197918XRCC2c.629A>G (p.Lys210Arg)
c.797A>G (p.Lys266Arg)
n.819A>G
7g.152648688T>GCA370197919XRCC2c.629A>C (p.Lys210Thr)
c.797A>C (p.Lys266Thr)
n.819A>C
7g.152648689T>ACA370197920XRCC2c.628A>T (p.Lys210Ter)
c.796A>T (p.Lys266Ter)
n.818A>T
7g.152648689T>CCA169486936XRCC2c.628A>G (p.Lys210Glu)
c.796A>G (p.Lys266Glu)
n.818A>G
 dbSNP
7g.152648689T>GCA370197921XRCC2c.628A>C (p.Lys210Gln)
c.796A>C (p.Lys266Gln)
n.818A>C
7g.152648689T=CA1753246546XRCC2c.628A= (p.Lys210=)
c.796A= (p.Lys266=)
n.818A=
7g.152648689_152648692delinsTTAACA1753246547XRCC2c.625_628delinsTTAA (p.Leu209=)
c.793_796delinsTTAA (p.Leu265=)
n.815_818delinsTTAA
7g.152648690T>ACA370197922XRCC2c.627A>T (p.Leu209Phe)
c.795A>T (p.Leu265Phe)
n.817A>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648690T>CCA458895200XRCC2c.627A>G (p.Leu209=)
c.795A>G (p.Leu265=)
n.817A>G
7g.152648690T>GCA370197923XRCC2c.627A>C (p.Leu209Phe)
c.795A>C (p.Leu265Phe)
n.817A>C
7g.152648690T=CA1753246548XRCC2c.627A= (p.Leu209=)
c.795A= (p.Leu265=)
n.817A=
7g.152648690_152648691delinsTACA1753246549XRCC2c.626_627delinsTA (p.Leu209=)
c.794_795delinsTA (p.Leu265=)
n.816_817delinsTA
7g.152648690_152648692delCA835377062XRCC2c.625_627del (p.Leu209del)
c.793_795del (p.Leu265del)
n.815_817del
 dbSNP
7g.152648691A=CA1753246557XRCC2c.626T= (p.Leu209=)
c.794T= (p.Leu265=)
n.816T=
7g.152648691A>CCA370197924XRCC2c.626T>G (p.Leu209Ter)
c.794T>G (p.Leu265Ter)
n.816T>G
 ClinVar dbSNP
7g.152648691A>GCA4582293XRCC2c.626T>C (p.Leu209Ser)
c.794T>C (p.Leu265Ser)
n.816T>C
 ClinVar dbSNP ExAC gnomAD v2
7g.152648691A>TCA4582294XRCC2c.626T>A (p.Leu209Ter)
c.794T>A (p.Leu265Ter)
n.816T>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648693delCA1139660349XRCC2c.626del (p.Leu209Ter)
c.794del (p.Leu265Ter)
n.816del
 ClinVar dbSNP
7g.152648692A=CA1753246558XRCC2c.625T= (p.Leu209=)
c.793T= (p.Leu265=)
n.815T=
7g.152648692A>CCA370197925XRCC2c.625T>G (p.Leu209Val)
c.793T>G (p.Leu265Val)
n.815T>G
7g.152648692A>GCA458895201XRCC2c.625T>C (p.Leu209=)
c.793T>C (p.Leu265=)
n.815T>C
 ClinVar
7g.152648692A>TCA370197926XRCC2c.625T>A (p.Leu209Ile)
c.793T>A (p.Leu265Ile)
n.815T>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648693A=CA1753246559XRCC2c.624T= (p.Ser208=)
c.792T= (p.Ser264=)
n.814T=
7g.152648693A>CCA370197927XRCC2c.624T>G (p.Ser208Arg)
c.792T>G (p.Ser264Arg)
n.814T>G
7g.152648693A>GCA458895202XRCC2c.624T>C (p.Ser208=)
c.792T>C (p.Ser264=)
n.814T>C
 ClinVar
7g.152648693A>TCA370197928XRCC2c.624T>A (p.Ser208Arg)
c.792T>A (p.Ser264Arg)
n.814T>A
 dbSNP gnomAD v3 gnomAD v4
7g.152648694C>ACA370197929XRCC2c.623G>T (p.Ser208Ile)
c.791G>T (p.Ser264Ile)
n.813G>T
 gnomAD v4
7g.152648694C>GCA370197930XRCC2c.623G>C (p.Ser208Thr)
c.791G>C (p.Ser264Thr)
n.813G>C
7g.152648694C>TCA370197931XRCC2c.623G>A (p.Ser208Asn)
c.791G>A (p.Ser264Asn)
n.813G>A
 ClinVar gnomAD v4
7g.152648694_152648696delinsCTGCA1753246560XRCC2c.621_623delinsCAG (p.Asn207=)
c.789_791delinsCAG (p.Asn263=)
n.811_813delinsCAG
7g.152648695T>ACA370197934XRCC2c.622A>T (p.Ser208Cys)
c.790A>T (p.Ser264Cys)
n.812A>T
7g.152648695T>CCA370197932XRCC2c.622A>G (p.Ser208Gly)
c.790A>G (p.Ser264Gly)
n.812A>G
7g.152648695T>GCA370197933XRCC2c.622A>C (p.Ser208Arg)
c.790A>C (p.Ser264Arg)
n.812A>C
 gnomAD v4
7g.152648696_152648697delCA16612057XRCC2c.621_622del (p.Asn207LysfsTer15)
c.789_790del (p.Asn263LysfsTer15)
n.811_812del
 ClinVar dbSNP
7g.152648696G>ACA458895203XRCC2c.621C>T (p.Asn207=)
c.789C>T (p.Asn263=)
n.811C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648696G>CCA370197935XRCC2c.621C>G (p.Asn207Lys)
c.789C>G (p.Asn263Lys)
n.811C>G
 ClinVar dbSNP
7g.152648696G=CA1753246563XRCC2c.621C= (p.Asn207=)
c.789C= (p.Asn263=)
n.811C=
7g.152648696G>TCA370197936XRCC2c.621C>A (p.Asn207Lys)
c.789C>A (p.Asn263Lys)
n.811C>A
7g.152648697T>ACA370197937XRCC2c.620A>T (p.Asn207Ile)
c.788A>T (p.Asn263Ile)
n.810A>T
7g.152648697T>CCA370197938XRCC2c.620A>G (p.Asn207Ser)
c.788A>G (p.Asn263Ser)
n.810A>G
7g.152648697T>GCA370197939XRCC2c.620A>C (p.Asn207Thr)
c.788A>C (p.Asn263Thr)
n.810A>C
7g.152648697_152648700delinsTTACCA1753246564XRCC2c.617_620delinsGTAA (p.Ser206=)
c.785_788delinsGTAA (p.Ser262=)
n.807_810delinsGTAA
7g.152648698T>ACA370197940XRCC2c.619A>T (p.Asn207Tyr)
c.787A>T (p.Asn263Tyr)
n.809A>T
7g.152648698T>CCA370197941XRCC2c.619A>G (p.Asn207Asp)
c.787A>G (p.Asn263Asp)
n.809A>G
 dbSNP
7g.152648698T>GCA370197942XRCC2c.619A>C (p.Asn207His)
c.787A>C (p.Asn263His)
n.809A>C
7g.152648698T=CA1753246566XRCC2c.619A= (p.Asn207=)
c.787A= (p.Asn263=)
n.809A=
7g.152648699_152648701delCA835377101XRCC2c.617_619del (p.Ser206del)
c.785_787del (p.Ser262del)
n.807_809del
 dbSNP gnomAD v3 gnomAD v4
7g.152648698_152648709delinsTACTTTTTAAACCA1753246565XRCC2c.608_619delinsGTTTAAAAAGTA (p.Cys203=)
c.776_787delinsGTTTAAAAAGTA (p.Cys259=)
n.798_809delinsGTTTAAAAAGTA
7g.152648699A>CCA370197943XRCC2c.618T>G (p.Ser206Arg)
c.786T>G (p.Ser262Arg)
n.808T>G
7g.152648699A>GCA458895204XRCC2c.618T>C (p.Ser206=)
c.786T>C (p.Ser262=)
n.808T>C
7g.152648699A>TCA370197944XRCC2c.618T>A (p.Ser206Arg)
c.786T>A (p.Ser262Arg)
n.808T>A
7g.152648699_152648709delinsGTTTACA288149XRCC2c.608_618delinsTAAAC (p.Cys203_Ser206delinsLeuAsn)
c.776_786delinsTAAAC (p.Cys259_Ser262delinsLeuAsn)
n.798_808delinsTAAAC
 ClinVar dbSNP
7g.152648700C>ACA370197946XRCC2c.617G>T (p.Ser206Ile)
c.785G>T (p.Ser262Ile)
n.807G>T
7g.152648700C>GCA370197947XRCC2c.617G>C (p.Ser206Thr)
c.785G>C (p.Ser262Thr)
n.807G>C
 gnomAD v4
7g.152648700C>TCA370197945XRCC2c.617G>A (p.Ser206Asn)
c.785G>A (p.Ser262Asn)
n.807G>A
7g.152648701T>ACA370197948XRCC2c.616A>T (p.Ser206Cys)
c.784A>T (p.Ser262Cys)
n.806A>T
7g.152648701T>CCA370197949XRCC2c.616A>G (p.Ser206Gly)
c.784A>G (p.Ser262Gly)
n.806A>G
 ClinVar
7g.152648701T>GCA370197950XRCC2c.616A>C (p.Ser206Arg)
c.784A>C (p.Ser262Arg)
n.806A>C
7g.152648702T>ACA370197951XRCC2c.615A>T (p.Lys205Asn)
c.783A>T (p.Lys261Asn)
n.805A>T
7g.152648702T>CCA458895208XRCC2c.615A>G (p.Lys205=)
c.783A>G (p.Lys261=)
n.805A>G
7g.152648702T>GCA370197952XRCC2c.615A>C (p.Lys205Asn)
c.783A>C (p.Lys261Asn)
n.805A>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648702T=CA1753246569XRCC2c.615A= (p.Lys205=)
c.783A= (p.Lys261=)
n.805A=
7g.152648703T>ACA370197953XRCC2c.614A>T (p.Lys205Ile)
c.782A>T (p.Lys261Ile)
n.804A>T
7g.152648703T>CCA370197954XRCC2c.614A>G (p.Lys205Arg)
c.782A>G (p.Lys261Arg)
n.804A>G
7g.152648703T>GCA4582295XRCC2c.614A>C (p.Lys205Thr)
c.782A>C (p.Lys261Thr)
n.804A>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648703T=CA1753246572XRCC2c.614A= (p.Lys205=)
c.782A= (p.Lys261=)
n.804A=
7g.152648704T>ACA370197955XRCC2c.613A>T (p.Lys205Ter)
c.781A>T (p.Lys261Ter)
n.803A>T
7g.152648704T>CCA370197956XRCC2c.613A>G (p.Lys205Glu)
c.781A>G (p.Lys261Glu)
n.803A>G
7g.152648704T>GCA370197957XRCC2c.613A>C (p.Lys205Gln)
c.781A>C (p.Lys261Gln)
n.803A>C
7g.152648705T>ACA370197958XRCC2c.612A>T (p.Leu204Phe)
c.780A>T (p.Leu260Phe)
n.802A>T
7g.152648705T>CCA458895212XRCC2c.612A>G (p.Leu204=)
c.780A>G (p.Leu260=)
n.802A>G
7g.152648705T>GCA370197959XRCC2c.612A>C (p.Leu204Phe)
c.780A>C (p.Leu260Phe)
n.802A>C
7g.152648706A>CCA370197962XRCC2c.611T>G (p.Leu204Ter)
c.779T>G (p.Leu260Ter)
n.801T>G
7g.152648706A>GCA370197961XRCC2c.611T>C (p.Leu204Ser)
c.779T>C (p.Leu260Ser)
n.801T>C
7g.152648706A>TCA370197960XRCC2c.611T>A (p.Leu204Ter)
c.779T>A (p.Leu260Ter)
n.801T>A
7g.152648706_152648709delinsAAACCA1753246575XRCC2c.608_611delinsGTTT (p.Cys203=)
c.776_779delinsGTTT (p.Cys259=)
n.798_801delinsGTTT
7g.152648707A>CCA370197963XRCC2c.610T>G (p.Leu204Val)
c.778T>G (p.Leu260Val)
n.800T>G
7g.152648707A>GCA458895213XRCC2c.610T>C (p.Leu204=)
c.778T>C (p.Leu260=)
n.800T>C
7g.152648707A>TCA370197964XRCC2c.610T>A (p.Leu204Ile)
c.778T>A (p.Leu260Ile)
n.800T>A
7g.152648710_152648712delCA1108857602XRCC2c.608_610del (p.Cys203del)
c.776_778del (p.Cys259del)
n.798_800del
 dbSNP gnomAD v3 gnomAD v4
7g.152648708A=CA1753246579XRCC2c.609T= (p.Cys203=)
c.777T= (p.Cys259=)
n.799T=
7g.152648708A>CCA370197965XRCC2c.609T>G (p.Cys203Trp)
c.777T>G (p.Cys259Trp)
n.799T>G
7g.152648708A>GCA4582296XRCC2c.609T>C (p.Cys203=)
c.777T>C (p.Cys259=)
n.799T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648708A>TCA370197966XRCC2c.609T>A (p.Cys203Ter)
c.777T>A (p.Cys259Ter)
n.799T>A
7g.152648709C>ACA370197967XRCC2c.608G>T (p.Cys203Phe)
c.776G>T (p.Cys259Phe)
n.798G>T
7g.152648709C>GCA370197968XRCC2c.608G>C (p.Cys203Ser)
c.776G>C (p.Cys259Ser)
n.798G>C
7g.152648709C>TCA370197969XRCC2c.608G>A (p.Cys203Tyr)
c.776G>A (p.Cys259Tyr)
n.798G>A
 ClinVar dbSNP gnomAD v4
7g.152648710A>CCA370197970XRCC2c.607T>G (p.Cys203Gly)
c.775T>G (p.Cys259Gly)
n.797T>G
7g.152648710A>GCA370197971XRCC2c.607T>C (p.Cys203Arg)
c.775T>C (p.Cys259Arg)
n.797T>C
7g.152648710A>TCA370197972XRCC2c.607T>A (p.Cys203Ser)
c.775T>A (p.Cys259Ser)
n.797T>A
7g.152648711A>CCA458895218XRCC2c.606T>G (p.Arg202=)
c.774T>G (p.Arg258=)
n.796T>G
7g.152648711A>GCA458895217XRCC2c.606T>C (p.Arg202=)
c.774T>C (p.Arg258=)
n.796T>C
7g.152648711A>TCA458895216XRCC2c.606T>A (p.Arg202=)
c.774T>A (p.Arg258=)
n.796T>A
7g.152648712C>ACA370197973XRCC2c.605G>T (p.Arg202Leu)
c.773G>T (p.Arg258Leu)
n.795G>T
7g.152648712C=CA1753246582XRCC2c.605G= (p.Arg202=)
c.773G= (p.Arg258=)
n.795G=
7g.152648712C>GCA370197974XRCC2c.605G>C (p.Arg202Pro)
c.773G>C (p.Arg258Pro)
n.795G>C
7g.152648712C>TCA288147XRCC2c.605G>A (p.Arg202His)
c.773G>A (p.Arg258His)
n.795G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648713G>ACA4582297XRCC2c.604C>T (p.Arg202Cys)
c.772C>T (p.Arg258Cys)
n.794C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648713G>CCA370197976XRCC2c.604C>G (p.Arg202Gly)
c.772C>G (p.Arg258Gly)
n.794C>G
7g.152648713G=CA1753246586XRCC2c.604C= (p.Arg202=)
c.772C= (p.Arg258=)
n.794C=
7g.152648713G>TCA370197975XRCC2c.604C>A (p.Arg202Ser)
c.772C>A (p.Arg258Ser)
n.794C>A
7g.152648714T>ACA458895219XRCC2c.603A>T (p.Ser201=)
c.771A>T (p.Ser257=)
n.793A>T
7g.152648714T>CCA458895220XRCC2c.603A>G (p.Ser201=)
c.771A>G (p.Ser257=)
n.793A>G
7g.152648714T>GCA458895222XRCC2c.603A>C (p.Ser201=)
c.771A>C (p.Ser257=)
n.793A>C
7g.152648715G>ACA300485XRCC2c.602C>T (p.Ser201Leu)
c.770C>T (p.Ser257Leu)
n.792C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648715G>CCA370197977XRCC2c.602C>G (p.Ser201Ter)
c.770C>G (p.Ser257Ter)
n.792C>G
7g.152648715G=CA1753246592XRCC2c.602C= (p.Ser201=)
c.770C= (p.Ser257=)
n.792C=
7g.152648715G>TCA370197978XRCC2c.602C>A (p.Ser201Ter)
c.770C>A (p.Ser257Ter)
n.792C>A
 dbSNP gnomAD v4
7g.152648716A>CCA370197979XRCC2c.601T>G (p.Ser201Ala)
c.769T>G (p.Ser257Ala)
n.791T>G
7g.152648716A>GCA370197980XRCC2c.601T>C (p.Ser201Pro)
c.769T>C (p.Ser257Pro)
n.791T>C
7g.152648716A>TCA370197981XRCC2c.601T>A (p.Ser201Thr)
c.769T>A (p.Ser257Thr)
n.791T>A
7g.152648717A>CCA458895223XRCC2c.600T>G (p.Val200=)
c.768T>G (p.Val256=)
n.790T>G
7g.152648717A>GCA458895224XRCC2c.600T>C (p.Val200=)
c.768T>C (p.Val256=)
n.790T>C
7g.152648717A>TCA458895225XRCC2c.600T>A (p.Val200=)
c.768T>A (p.Val256=)
n.790T>A
7g.152648717_152648718delinsAACA1753246597XRCC2c.599_600delinsTT (p.Val200=)
c.767_768delinsTT (p.Val256=)
n.789_790delinsTT
7g.152648717_152648718delinsCTCA16618425XRCC2c.599_600delinsAG (p.Val200Glu)
c.767_768delinsAG (p.Val256Glu)
n.789_790delinsAG
 ClinVar dbSNP
7g.152648718A>CCA370197984XRCC2c.599T>G (p.Val200Gly)
c.767T>G (p.Val256Gly)
n.789T>G
 COSMIC
7g.152648718A>GCA370197982XRCC2c.599T>C (p.Val200Ala)
c.767T>C (p.Val256Ala)
n.789T>C
7g.152648718A>TCA370197983XRCC2c.599T>A (p.Val200Asp)
c.767T>A (p.Val256Asp)
n.789T>A
7g.152648719C>ACA370197985XRCC2c.598G>T (p.Val200Phe)
c.766G>T (p.Val256Phe)
n.788G>T
7g.152648719C>GCA370197986XRCC2c.598G>C (p.Val200Leu)
c.766G>C (p.Val256Leu)
n.788G>C
7g.152648719C>TCA370197987XRCC2c.598G>A (p.Val200Ile)
c.766G>A (p.Val256Ile)
n.788G>A
 dbSNP
7g.152648720T>ACA370197988XRCC2c.597A>T (p.Leu199Phe)
c.765A>T (p.Leu255Phe)
n.787A>T
7g.152648720T>CCA458895228XRCC2c.597A>G (p.Leu199=)
c.765A>G (p.Leu255=)
n.787A>G
7g.152648720T>GCA370197989XRCC2c.597A>C (p.Leu199Phe)
c.765A>C (p.Leu255Phe)
n.787A>C
7g.152648721A=CA1753246604XRCC2c.596T= (p.Leu199=)
c.764T= (p.Leu255=)
n.786T=
7g.152648721A>CCA4582298XRCC2c.596T>G (p.Leu199Ter)
c.764T>G (p.Leu255Ter)
n.786T>G
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648721A>GCA370197991XRCC2c.596T>C (p.Leu199Ser)
c.764T>C (p.Leu255Ser)
n.786T>C
7g.152648721A>TCA370197990XRCC2c.596T>A (p.Leu199Ter)
c.764T>A (p.Leu255Ter)
n.786T>A
7g.152648722A>CCA370197992XRCC2c.595T>G (p.Leu199Val)
c.763T>G (p.Leu255Val)
n.785T>G
7g.152648722A>GCA458895229XRCC2c.595T>C (p.Leu199=)
c.763T>C (p.Leu255=)
n.785T>C
7g.152648722A>TCA370197993XRCC2c.595T>A (p.Leu199Ile)
c.763T>A (p.Leu255Ile)
n.785T>A
7g.152648723T>ACA458895230XRCC2c.594A>T (p.Ser198=)
c.762A>T (p.Ser254=)
n.784A>T
7g.152648723T>CCA458895231XRCC2c.594A>G (p.Ser198=)
c.762A>G (p.Ser254=)
n.784A>G
7g.152648723T>GCA458895232XRCC2c.594A>C (p.Ser198=)
c.762A>C (p.Ser254=)
n.784A>C
7g.152648724G>ACA370197994XRCC2c.593C>T (p.Ser198Leu)
c.761C>T (p.Ser254Leu)
n.783C>T
 dbSNP
7g.152648724G>CCA370197995XRCC2c.593C>G (p.Ser198Ter)
c.761C>G (p.Ser254Ter)
n.783C>G
7g.152648724G=CA1753246607XRCC2c.593C= (p.Ser198=)
c.761C= (p.Ser254=)
n.783C=
7g.152648724G>TCA370197996XRCC2c.593C>A (p.Ser198Ter)
c.761C>A (p.Ser254Ter)
n.783C>A
 dbSNP gnomAD v2 gnomAD v4
7g.152648725A>CCA370197997XRCC2c.592T>G (p.Ser198Ala)
c.760T>G (p.Ser254Ala)
n.782T>G
7g.152648725A>GCA370197998XRCC2c.592T>C (p.Ser198Pro)
c.760T>C (p.Ser254Pro)
n.782T>C
7g.152648725A>TCA370197999XRCC2c.592T>A (p.Ser198Thr)
c.760T>A (p.Ser254Thr)
n.782T>A
7g.152648726A>CCA370198000XRCC2c.591T>G (p.Phe197Leu)
c.759T>G (p.Phe253Leu)
n.781T>G
7g.152648726A>GCA458895233XRCC2c.591T>C (p.Phe197=)
c.759T>C (p.Phe253=)
n.781T>C
7g.152648726A>TCA370198001XRCC2c.591T>A (p.Phe197Leu)
c.759T>A (p.Phe253Leu)
n.781T>A
 ClinVar
7g.152648727A>CCA370198004XRCC2c.590T>G (p.Phe197Cys)
c.758T>G (p.Phe253Cys)
n.780T>G
7g.152648727A>GCA370198003XRCC2c.590T>C (p.Phe197Ser)
c.758T>C (p.Phe253Ser)
n.780T>C
7g.152648727A>TCA370198002XRCC2c.590T>A (p.Phe197Tyr)
c.758T>A (p.Phe253Tyr)
n.780T>A
7g.152648727_152648729delCA2580077736XRCC2c.588_590del (p.Gln196_Phe197delinsHis)
c.756_758del (p.Gln252_Phe253delinsHis)
n.778_780del
 ClinVar
7g.152648728A>CCA370198005XRCC2c.589T>G (p.Phe197Val)
c.757T>G (p.Phe253Val)
n.779T>G
7g.152648728A>GCA370198007XRCC2c.589T>C (p.Phe197Leu)
c.757T>C (p.Phe253Leu)
n.779T>C
7g.152648728A>TCA370198006XRCC2c.589T>A (p.Phe197Ile)
c.757T>A (p.Phe253Ile)
n.779T>A
7g.152648729T>ACA370198008XRCC2c.588A>T (p.Gln196His)
c.756A>T (p.Gln252His)
n.778A>T
7g.152648729T>CCA458895234XRCC2c.588A>G (p.Gln196=)
c.756A>G (p.Gln252=)
n.778A>G
 ClinVar dbSNP
7g.152648729T>GCA370198009XRCC2c.588A>C (p.Gln196His)
c.756A>C (p.Gln252His)
n.778A>C
7g.152648729T=CA1753246612XRCC2c.588A= (p.Gln196=)
c.756A= (p.Gln252=)
n.778A=
7g.152648730T>ACA370198010XRCC2c.587A>T (p.Gln196Leu)
c.755A>T (p.Gln252Leu)
n.777A>T
7g.152648730T>CCA370198012XRCC2c.587A>G (p.Gln196Arg)
c.755A>G (p.Gln252Arg)
n.777A>G
7g.152648730T>GCA370198011XRCC2c.587A>C (p.Gln196Pro)
c.755A>C (p.Gln252Pro)
n.777A>C
7g.152648731G>ACA370198013XRCC2c.586C>T (p.Gln196Ter)
c.754C>T (p.Gln252Ter)
n.776C>T
7g.152648731G>CCA370198015XRCC2c.586C>G (p.Gln196Glu)
c.754C>G (p.Gln252Glu)
n.776C>G
 ClinVar dbSNP gnomAD v4
7g.152648731G=CA1753246617XRCC2c.586C= (p.Gln196=)
c.754C= (p.Gln252=)
n.776C=
7g.152648731G>TCA370198014XRCC2c.586C>A (p.Gln196Lys)
c.754C>A (p.Gln252Lys)
n.776C>A
7g.152648732G>ACA458895239XRCC2c.585C>T (p.Asn195=)
c.753C>T (p.Asn251=)
n.775C>T
 ClinVar dbSNP
7g.152648732G>CCA4582299XRCC2c.585C>G (p.Asn195Lys)
c.753C>G (p.Asn251Lys)
n.775C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648732G=CA1753246623XRCC2c.585C= (p.Asn195=)
c.753C= (p.Asn251=)
n.775C=
7g.152648732G>TCA370198016XRCC2c.585C>A (p.Asn195Lys)
c.753C>A (p.Asn251Lys)
n.775C>A
7g.152648733T>ACA370198017XRCC2c.584A>T (p.Asn195Ile)
c.752A>T (p.Asn251Ile)
n.774A>T
7g.152648733T>CCA370198019XRCC2c.584A>G (p.Asn195Ser)
c.752A>G (p.Asn251Ser)
n.774A>G
7g.152648733T>GCA370198018XRCC2c.584A>C (p.Asn195Thr)
c.752A>C (p.Asn251Thr)
n.774A>C
7g.152648734T>ACA370198020XRCC2c.583A>T (p.Asn195Tyr)
c.751A>T (p.Asn251Tyr)
n.773A>T
7g.152648734T>CCA370198022XRCC2c.583A>G (p.Asn195Asp)
c.751A>G (p.Asn251Asp)
n.773A>G
7g.152648734T>GCA370198021XRCC2c.583A>C (p.Asn195His)
c.751A>C (p.Asn251His)
n.773A>C
 gnomAD v4
7g.152648735G>ACA458895241XRCC2c.582C>T (p.Ser194=)
c.750C>T (p.Ser250=)
n.772C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648735G>CCA370198023XRCC2c.582C>G (p.Ser194Arg)
c.750C>G (p.Ser250Arg)
n.772C>G
7g.152648735G=CA1753246636XRCC2c.582C= (p.Ser194=)
c.750C= (p.Ser250=)
n.772C=
7g.152648735G>TCA370198024XRCC2c.582C>A (p.Ser194Arg)
c.750C>A (p.Ser250Arg)
n.772C>A
7g.152648736C>ACA370198025XRCC2c.581G>T (p.Ser194Ile)
c.749G>T (p.Ser250Ile)
n.771G>T
7g.152648736C=CA1753246640XRCC2c.581G= (p.Ser194=)
c.749G= (p.Ser250=)
n.771G=
7g.152648736C>GCA370198026XRCC2c.581G>C (p.Ser194Thr)
c.749G>C (p.Ser250Thr)
n.771G>C
 ClinVar dbSNP
7g.152648736C>TCA370198027XRCC2c.581G>A (p.Ser194Asn)
c.749G>A (p.Ser250Asn)
n.771G>A
7g.152648737T>ACA370198028XRCC2c.580A>T (p.Ser194Cys)
c.748A>T (p.Ser250Cys)
n.770A>T
7g.152648737T>CCA370198029XRCC2c.580A>G (p.Ser194Gly)
c.748A>G (p.Ser250Gly)
n.770A>G
 dbSNP
7g.152648737T>GCA370198030XRCC2c.580A>C (p.Ser194Arg)
c.748A>C (p.Ser250Arg)
n.770A>C
7g.152648737T=CA1753246644XRCC2c.580A= (p.Ser194=)
c.748A= (p.Ser250=)
n.770A=
7g.152648738G>ACA4582300XRCC2c.579C>T (p.Ser193=)
c.747C>T (p.Ser249=)
n.769C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648738G>CCA370198031XRCC2c.579C>G (p.Ser193Arg)
c.747C>G (p.Ser249Arg)
n.769C>G
7g.152648738G=CA1753246651XRCC2c.579C= (p.Ser193=)
c.747C= (p.Ser249=)
n.769C=
7g.152648738G>TCA370198032XRCC2c.579C>A (p.Ser193Arg)
c.747C>A (p.Ser249Arg)
n.769C>A
7g.152648739C>ACA370198034XRCC2c.578G>T (p.Ser193Ile)
c.746G>T (p.Ser249Ile)
n.768G>T
7g.152648739C=CA1753246654XRCC2c.578G= (p.Ser193=)
c.746G= (p.Ser249=)
n.768G=
7g.152648739C>GCA4582301XRCC2c.578G>C (p.Ser193Thr)
c.746G>C (p.Ser249Thr)
n.768G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648739C>TCA370198033XRCC2c.578G>A (p.Ser193Asn)
c.746G>A (p.Ser249Asn)
n.768G>A
7g.152648742_152648754dupCA2579071949XRCC2c.566_578dup (p.Ser193ArgfsTer2)
c.734_746dup (p.Ser249ArgfsTer2)
n.756_768dup
 ClinVar
7g.152648740T>ACA370198035XRCC2c.577A>T (p.Ser193Cys)
c.745A>T (p.Ser249Cys)
n.767A>T
7g.152648740T>CCA370198036XRCC2c.577A>G (p.Ser193Gly)
c.745A>G (p.Ser249Gly)
n.767A>G
7g.152648740T>GCA370198037XRCC2c.577A>C (p.Ser193Arg)
c.745A>C (p.Ser249Arg)
n.767A>C
7g.152648741T>ACA370198038XRCC2c.576A>T (p.Gln192His)
c.744A>T (p.Gln248His)
n.766A>T
7g.152648741T>CCA458895243XRCC2c.576A>G (p.Gln192=)
c.744A>G (p.Gln248=)
n.766A>G
7g.152648741T>GCA4582302XRCC2c.576A>C (p.Gln192His)
c.744A>C (p.Gln248His)
n.766A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648741T=CA1753246657XRCC2c.576A= (p.Gln192=)
c.744A= (p.Gln248=)
n.766A=
7g.152648742T>ACA370198039XRCC2c.575A>T (p.Gln192Leu)
c.743A>T (p.Gln248Leu)
n.765A>T
7g.152648742T>CCA169486937XRCC2c.575A>G (p.Gln192Arg)
c.743A>G (p.Gln248Arg)
n.765A>G
 dbSNP
7g.152648742T>GCA370198040XRCC2c.575A>C (p.Gln192Pro)
c.743A>C (p.Gln248Pro)
n.765A>C
 ClinVar gnomAD v4
7g.152648742T=CA1753246661XRCC2c.575A= (p.Gln192=)
c.743A= (p.Gln248=)
n.765A=
7g.152648743G>ACA370198041XRCC2c.574C>T (p.Gln192Ter)
c.742C>T (p.Gln248Ter)
n.764C>T
 dbSNP
7g.152648743G>CCA4582303XRCC2c.574C>G (p.Gln192Glu)
c.742C>G (p.Gln248Glu)
n.764C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648743G=CA1753246664XRCC2c.574C= (p.Gln192=)
c.742C= (p.Gln248=)
n.764C=
7g.152648743G>TCA370198042XRCC2c.574C>A (p.Gln192Lys)
c.742C>A (p.Gln248Lys)
n.764C>A
7g.152648744A>CCA458895244XRCC2c.573T>G (p.Ser191=)
c.741T>G (p.Ser247=)
n.763T>G
7g.152648744A>GCA458895245XRCC2c.573T>C (p.Ser191=)
c.741T>C (p.Ser247=)
n.763T>C
7g.152648744A>TCA458895246XRCC2c.573T>A (p.Ser191=)
c.741T>A (p.Ser247=)
n.763T>A
7g.152648745G>ACA4582304XRCC2c.572C>T (p.Ser191Phe)
c.740C>T (p.Ser247Phe)
n.762C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648745G>CCA370198044XRCC2c.572C>G (p.Ser191Cys)
c.740C>G (p.Ser247Cys)
n.762C>G
 ClinVar gnomAD v4
7g.152648745G=CA1753246670XRCC2c.572C= (p.Ser191=)
c.740C= (p.Ser247=)
n.762C=
7g.152648745G>TCA370198043XRCC2c.572C>A (p.Ser191Tyr)
c.740C>A (p.Ser247Tyr)
n.762C>A
7g.152648746A>CCA370198045XRCC2c.571T>G (p.Ser191Ala)
c.739T>G (p.Ser247Ala)
n.761T>G
7g.152648746A>GCA370198046XRCC2c.571T>C (p.Ser191Pro)
c.739T>C (p.Ser247Pro)
n.761T>C
 ClinVar gnomAD v4
7g.152648746A>TCA370198047XRCC2c.571T>A (p.Ser191Thr)
c.739T>A (p.Ser247Thr)
n.761T>A
7g.152648747A>CCA370198048XRCC2c.570T>G (p.Asp190Glu)
c.738T>G (p.Asp246Glu)
n.760T>G
7g.152648747A>GCA458895247XRCC2c.570T>C (p.Asp190=)
c.738T>C (p.Asp246=)
n.760T>C
7g.152648747A>TCA370198049XRCC2c.570T>A (p.Asp190Glu)
c.738T>A (p.Asp246Glu)
n.760T>A
7g.152648748T>ACA370198050XRCC2c.569A>T (p.Asp190Val)
c.737A>T (p.Asp246Val)
n.759A>T
7g.152648748T>CCA370198051XRCC2c.569A>G (p.Asp190Gly)
c.737A>G (p.Asp246Gly)
n.759A>G
7g.152648748T>GCA370198052XRCC2c.569A>C (p.Asp190Ala)
c.737A>C (p.Asp246Ala)
n.759A>C
7g.152648749C>ACA370198053XRCC2c.568G>T (p.Asp190Tyr)
c.736G>T (p.Asp246Tyr)
n.758G>T
 dbSNP
7g.152648749C>GCA370198054XRCC2c.568G>C (p.Asp190His)
c.736G>C (p.Asp246His)
n.758G>C
7g.152648749C>TCA370198055XRCC2c.568G>A (p.Asp190Asn)
c.736G>A (p.Asp246Asn)
n.758G>A
7g.152648750A>CCA370198056XRCC2c.567T>G (p.Asp189Glu)
c.735T>G (p.Asp245Glu)
n.757T>G
7g.152648750A>GCA458895248XRCC2c.567T>C (p.Asp189=)
c.735T>C (p.Asp245=)
n.757T>C
7g.152648750A>TCA370198057XRCC2c.567T>A (p.Asp189Glu)
c.735T>A (p.Asp245Glu)
n.757T>A
7g.152648751T>ACA169486938XRCC2c.566A>T (p.Asp189Val)
c.734A>T (p.Asp245Val)
n.756A>T
 ClinVar dbSNP
7g.152648751T>CCA4582305XRCC2c.566A>G (p.Asp189Gly)
c.734A>G (p.Asp245Gly)
n.756A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648751T>GCA370198058XRCC2c.566A>C (p.Asp189Ala)
c.734A>C (p.Asp245Ala)
n.756A>C
7g.152648751T=CA1753246677XRCC2c.566A= (p.Asp189=)
c.734A= (p.Asp245=)
n.756A=
7g.152648752C>ACA169486939XRCC2c.565G>T (p.Asp189Tyr)
c.733G>T (p.Asp245Tyr)
n.755G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648752C=CA1753246682XRCC2c.565G= (p.Asp189=)
c.733G= (p.Asp245=)
n.755G=
7g.152648752C>GCA370198059XRCC2c.565G>C (p.Asp189His)
c.733G>C (p.Asp245His)
n.755G>C
7g.152648752C>TCA370198060XRCC2c.565G>A (p.Asp189Asn)
c.733G>A (p.Asp245Asn)
n.755G>A
7g.152648752_152648754delinsCTTCA1753246684XRCC2c.563_565delinsAAG (p.Gln188=)
c.731_733delinsAAG (p.Gln244=)
n.753_755delinsAAG
7g.152648753T>ACA370198061XRCC2c.564A>T (p.Gln188His)
c.732A>T (p.Gln244His)
n.754A>T
7g.152648753T>CCA458895250XRCC2c.564A>G (p.Gln188=)
c.732A>G (p.Gln244=)
n.754A>G
7g.152648753T>GCA370198062XRCC2c.564A>C (p.Gln188His)
c.732A>C (p.Gln244His)
n.754A>C
7g.152648753_152648754delCA916082967XRCC2c.563_564del (p.Gln188ArgfsTer2)
c.731_732del (p.Gln244ArgfsTer2)
n.753_754del
 ClinVar dbSNP gnomAD v4
7g.152648754T>ACA370198063XRCC2c.563A>T (p.Gln188Leu)
c.731A>T (p.Gln244Leu)
n.753A>T
7g.152648754T>CCA370198064XRCC2c.563A>G (p.Gln188Arg)
c.731A>G (p.Gln244Arg)
n.753A>G
 ClinVar dbSNP gnomAD v4
7g.152648754T>GCA370198065XRCC2c.563A>C (p.Gln188Pro)
c.731A>C (p.Gln244Pro)
n.753A>C
7g.152648754T=CA1753246691XRCC2c.563A= (p.Gln188=)
c.731A= (p.Gln244=)
n.753A=
7g.152648755G>ACA16618426XRCC2c.562C>T (p.Gln188Ter)
c.730C>T (p.Gln244Ter)
n.752C>T
 ClinVar dbSNP gnomAD v4
7g.152648755G>CCA370198066XRCC2c.562C>G (p.Gln188Glu)
c.730C>G (p.Gln244Glu)
n.752C>G
 dbSNP gnomAD v4
7g.152648755G=CA1753246698XRCC2c.562C= (p.Gln188=)
c.730C= (p.Gln244=)
n.752C=
7g.152648755G>TCA370198067XRCC2c.562C>A (p.Gln188Lys)
c.730C>A (p.Gln244Lys)
n.752C>A
7g.152648756T>ACA370198068XRCC2c.561A>T (p.Lys187Asn)
c.729A>T (p.Lys243Asn)
n.751A>T
7g.152648756T>CCA458895253XRCC2c.561A>G (p.Lys187=)
c.729A>G (p.Lys243=)
n.751A>G
7g.152648756T>GCA370198069XRCC2c.561A>C (p.Lys187Asn)
c.729A>C (p.Lys243Asn)
n.751A>C

Number of alleles fetched