Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.152648742_152648754dupCA2579071949XRCC2c.566_578dup (p.Ser193ArgfsTer2)
c.734_746dup (p.Ser249ArgfsTer2)
n.756_768dup
 ClinVar
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
 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
7g.152648757T>ACA370198070XRCC2c.560A>T (p.Lys187Ile)
c.728A>T (p.Lys243Ile)
n.750A>T
7g.152648757T>CCA370198071XRCC2c.560A>G (p.Lys187Arg)
c.728A>G (p.Lys243Arg)
n.750A>G
 ClinVar dbSNP
7g.152648757T>GCA370198072XRCC2c.560A>C (p.Lys187Thr)
c.728A>C (p.Lys243Thr)
n.750A>C
 ClinVar dbSNP gnomAD v4
7g.152648757T=CA1753246702XRCC2c.560A= (p.Lys187=)
c.728A= (p.Lys243=)
n.750A=
7g.152648758T>ACA370198073XRCC2c.559A>T (p.Lys187Ter)
c.727A>T (p.Lys243Ter)
n.749A>T
7g.152648758T>CCA370198074XRCC2c.559A>G (p.Lys187Glu)
c.727A>G (p.Lys243Glu)
n.749A>G
 ClinVar
7g.152648758T>GCA370198075XRCC2c.559A>C (p.Lys187Gln)
c.727A>C (p.Lys243Gln)
n.749A>C
7g.152648759G>ACA458895257XRCC2c.558C>T (p.Ser186=)
c.726C>T (p.Ser242=)
n.748C>T
 ClinVar dbSNP gnomAD v4 COSMIC
7g.152648759G>CCA458895259XRCC2c.558C>G (p.Ser186=)
c.726C>G (p.Ser242=)
n.748C>G
7g.152648759G>TCA458895258XRCC2c.558C>A (p.Ser186=)
c.726C>A (p.Ser242=)
n.748C>A
7g.152648760G>ACA370198078XRCC2c.557C>T (p.Ser186Phe)
c.725C>T (p.Ser242Phe)
n.747C>T
 ClinVar dbSNP
7g.152648760G>CCA370198077XRCC2c.557C>G (p.Ser186Cys)
c.725C>G (p.Ser242Cys)
n.747C>G
7g.152648760G=CA1753246712XRCC2c.557C= (p.Ser186=)
c.725C= (p.Ser242=)
n.747C=
7g.152648760G>TCA370198076XRCC2c.557C>A (p.Ser186Tyr)
c.725C>A (p.Ser242Tyr)
n.747C>A
 dbSNP
7g.152648761A>CCA370198079XRCC2c.556T>G (p.Ser186Ala)
c.724T>G (p.Ser242Ala)
n.746T>G
7g.152648761A>GCA370198080XRCC2c.556T>C (p.Ser186Pro)
c.724T>C (p.Ser242Pro)
n.746T>C
7g.152648761A>TCA370198081XRCC2c.556T>A (p.Ser186Thr)
c.724T>A (p.Ser242Thr)
n.746T>A
7g.152648762G>ACA4582306XRCC2c.555C>T (p.Phe185=)
c.723C>T (p.Phe241=)
n.745C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648762G>CCA370198082XRCC2c.555C>G (p.Phe185Leu)
c.723C>G (p.Phe241Leu)
n.745C>G
7g.152648762G=CA1753246717XRCC2c.555C= (p.Phe185=)
c.723C= (p.Phe241=)
n.745C=
7g.152648762G>TCA370198083XRCC2c.555C>A (p.Phe185Leu)
c.723C>A (p.Phe241Leu)
n.745C>A
7g.152648763A>CCA370198084XRCC2c.554T>G (p.Phe185Cys)
c.722T>G (p.Phe241Cys)
n.744T>G
7g.152648763A>GCA370198086XRCC2c.554T>C (p.Phe185Ser)
c.722T>C (p.Phe241Ser)
n.744T>C
7g.152648763A>TCA370198085XRCC2c.554T>A (p.Phe185Tyr)
c.722T>A (p.Phe241Tyr)
n.744T>A
7g.152648764A>CCA370198087XRCC2c.553T>G (p.Phe185Val)
c.721T>G (p.Phe241Val)
n.743T>G
7g.152648764A>GCA370198088XRCC2c.553T>C (p.Phe185Leu)
c.721T>C (p.Phe241Leu)
n.743T>C
7g.152648764A>TCA370198089XRCC2c.553T>A (p.Phe185Ile)
c.721T>A (p.Phe241Ile)
n.743T>A
7g.152648765A=CA1753246720XRCC2c.552T= (p.Phe184=)
c.720T= (p.Phe240=)
n.742T=
7g.152648765A>CCA370198090XRCC2c.552T>G (p.Phe184Leu)
c.720T>G (p.Phe240Leu)
n.742T>G
7g.152648765A>GCA16605087XRCC2c.552T>C (p.Phe184=)
c.720T>C (p.Phe240=)
n.742T>C
 ClinVar dbSNP
7g.152648765A>TCA370198091XRCC2c.552T>A (p.Phe184Leu)
c.720T>A (p.Phe240Leu)
n.742T>A
7g.152648766A>CCA370198092XRCC2c.551T>G (p.Phe184Cys)
c.719T>G (p.Phe240Cys)
n.741T>G
7g.152648766A>GCA370198093XRCC2c.551T>C (p.Phe184Ser)
c.719T>C (p.Phe240Ser)
n.741T>C
7g.152648766A>TCA370198094XRCC2c.551T>A (p.Phe184Tyr)
c.719T>A (p.Phe240Tyr)
n.741T>A
7g.152648767A>CCA370198095XRCC2c.550T>G (p.Phe184Val)
c.718T>G (p.Phe240Val)
n.740T>G
 ClinVar
7g.152648767A>GCA370198096XRCC2c.550T>C (p.Phe184Leu)
c.718T>C (p.Phe240Leu)
n.740T>C
7g.152648767A>TCA370198097XRCC2c.550T>A (p.Phe184Ile)
c.718T>A (p.Phe240Ile)
n.740T>A
7g.152648768C>ACA370198098XRCC2c.549G>T (p.Met183Ile)
c.717G>T (p.Met239Ile)
n.739G>T
7g.152648768C>GCA370198100XRCC2c.549G>C (p.Met183Ile)
c.717G>C (p.Met239Ile)
n.739G>C
7g.152648768C>TCA370198099XRCC2c.549G>A (p.Met183Ile)
c.717G>A (p.Met239Ile)
n.739G>A
7g.152648769A>CCA370198101XRCC2c.548T>G (p.Met183Arg)
c.716T>G (p.Met239Arg)
n.738T>G
7g.152648769A>GCA370198102XRCC2c.548T>C (p.Met183Thr)
c.716T>C (p.Met239Thr)
n.738T>C
7g.152648769A>TCA370198103XRCC2c.548T>A (p.Met183Lys)
c.716T>A (p.Met239Lys)
n.738T>A
7g.152648770T>ACA370198104XRCC2c.547A>T (p.Met183Leu)
c.715A>T (p.Met239Leu)
n.737A>T
7g.152648770T>CCA370198105XRCC2c.547A>G (p.Met183Val)
c.715A>G (p.Met239Val)
n.737A>G
 dbSNP
7g.152648770T>GCA370198106XRCC2c.547A>C (p.Met183Leu)
c.715A>C (p.Met239Leu)
n.737A>C
7g.152648770T=CA1753246725XRCC2c.547A= (p.Met183=)
c.715A= (p.Met239=)
n.737A=
7g.152648771C>ACA370198107XRCC2c.546G>T (p.Arg182Ser)
c.714G>T (p.Arg238Ser)
n.736G>T
 dbSNP
7g.152648771C=CA1753246730XRCC2c.546G= (p.Arg182=)
c.714G= (p.Arg238=)
n.736G=
7g.152648771C>GCA4582307XRCC2c.546G>C (p.Arg182Ser)
c.714G>C (p.Arg238Ser)
n.736G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648771C>TCA458895268XRCC2c.546G>A (p.Arg182=)
c.714G>A (p.Arg238=)
n.736G>A
 gnomAD v4
7g.152648772C>ACA370198108XRCC2c.545G>T (p.Arg182Met)
c.713G>T (p.Arg238Met)
n.735G>T
7g.152648772C=CA1753246739XRCC2c.545G= (p.Arg182=)
c.713G= (p.Arg238=)
n.735G=
7g.152648772C>GCA370198109XRCC2c.545G>C (p.Arg182Thr)
c.713G>C (p.Arg238Thr)
n.735G>C
7g.152648772C>TCA16618427XRCC2c.545G>A (p.Arg182Lys)
c.713G>A (p.Arg238Lys)
n.735G>A
 ClinVar dbSNP gnomAD v4
7g.152648773T>ACA370198110XRCC2c.544A>T (p.Arg182Trp)
c.712A>T (p.Arg238Trp)
n.734A>T
 gnomAD v4
7g.152648773T>CCA370198111XRCC2c.544A>G (p.Arg182Gly)
c.712A>G (p.Arg238Gly)
n.734A>G
 dbSNP gnomAD v2 gnomAD v4
7g.152648773T>GCA458895271XRCC2c.544A>C (p.Arg182=)
c.712A>C (p.Arg238=)
n.734A>C
7g.152648773T=CA1753246742XRCC2c.544A= (p.Arg182=)
c.712A= (p.Arg238=)
n.734A=
7g.152648774G>ACA16605297XRCC2c.543C>T (p.His181=)
c.711C>T (p.His237=)
n.733C>T
 ClinVar dbSNP gnomAD v4
7g.152648774G>CCA370198113XRCC2c.543C>G (p.His181Gln)
c.711C>G (p.His237Gln)
n.733C>G
 gnomAD v4
7g.152648774G=CA1753246748XRCC2c.543C= (p.His181=)
c.711C= (p.His237=)
n.733C=
7g.152648774G>TCA370198112XRCC2c.543C>A (p.His181Gln)
c.711C>A (p.His237Gln)
n.733C>A
7g.152648775T>ACA370198114XRCC2c.542A>T (p.His181Leu)
c.710A>T (p.His237Leu)
n.732A>T
 ClinVar dbSNP
7g.152648775T>CCA370198115XRCC2c.542A>G (p.His181Arg)
c.710A>G (p.His237Arg)
n.732A>G
7g.152648775T>GCA370198116XRCC2c.542A>C (p.His181Pro)
c.710A>C (p.His237Pro)
n.732A>C
7g.152648776G>ACA370198117XRCC2c.541C>T (p.His181Tyr)
c.709C>T (p.His237Tyr)
n.731C>T
7g.152648776G>CCA370198118XRCC2c.541C>G (p.His181Asp)
c.709C>G (p.His237Asp)
n.731C>G
 dbSNP
7g.152648776G>TCA370198119XRCC2c.541C>A (p.His181Asn)
c.709C>A (p.His237Asn)
n.731C>A
7g.152648777C>ACA370198120XRCC2c.540G>T (p.Lys180Asn)
c.708G>T (p.Lys236Asn)
n.730G>T
7g.152648777C>GCA370198121XRCC2c.540G>C (p.Lys180Asn)
c.708G>C (p.Lys236Asn)
n.730G>C
7g.152648777C>TCA458895273XRCC2c.540G>A (p.Lys180=)
c.708G>A (p.Lys236=)
n.730G>A
 dbSNP
7g.152648778T>ACA370198122XRCC2c.539A>T (p.Lys180Met)
c.707A>T (p.Lys236Met)
n.729A>T
7g.152648778T>CCA370198123XRCC2c.539A>G (p.Lys180Arg)
c.707A>G (p.Lys236Arg)
n.729A>G
7g.152648778T>GCA370198124XRCC2c.539A>C (p.Lys180Thr)
c.707A>C (p.Lys236Thr)
n.729A>C
7g.152648779T>ACA370198126XRCC2c.538A>T (p.Lys180Ter)
c.706A>T (p.Lys236Ter)
n.728A>T
7g.152648779T>CCA370198127XRCC2c.538A>G (p.Lys180Glu)
c.706A>G (p.Lys236Glu)
n.728A>G
7g.152648779T>GCA370198125XRCC2c.538A>C (p.Lys180Gln)
c.706A>C (p.Lys236Gln)
n.728A>C
7g.152648780C>ACA458895274XRCC2c.537G>T (p.Val179=)
c.705G>T (p.Val235=)
n.727G>T
7g.152648780C>GCA458895275XRCC2c.537G>C (p.Val179=)
c.705G>C (p.Val235=)
n.727G>C
7g.152648780C>TCA458895276XRCC2c.537G>A (p.Val179=)
c.705G>A (p.Val235=)
n.727G>A
7g.152648781A=CA1753246751XRCC2c.536T= (p.Val179=)
c.704T= (p.Val235=)
n.726T=
7g.152648781A>CCA370198128XRCC2c.536T>G (p.Val179Gly)
c.704T>G (p.Val235Gly)
n.726T>G
7g.152648781A>GCA4582308XRCC2c.536T>C (p.Val179Ala)
c.704T>C (p.Val235Ala)
n.726T>C
 dbSNP ExAC gnomAD v2 COSMIC
7g.152648781A>TCA370198129XRCC2c.536T>A (p.Val179Glu)
c.704T>A (p.Val235Glu)
n.726T>A
7g.152648782C>ACA370198130XRCC2c.535G>T (p.Val179Leu)
c.703G>T (p.Val235Leu)
n.725G>T
 ClinVar gnomAD v4
7g.152648782C=CA1753246755XRCC2c.535G= (p.Val179=)
c.703G= (p.Val235=)
n.725G=
7g.152648782C>GCA370198131XRCC2c.535G>C (p.Val179Leu)
c.703G>C (p.Val235Leu)
n.725G>C
 ClinVar dbSNP gnomAD v4
7g.152648782C>TCA370198132XRCC2c.535G>A (p.Val179Met)
c.703G>A (p.Val235Met)
n.725G>A
7g.152648783C>ACA458895277XRCC2c.534G>T (p.Leu178=)
c.702G>T (p.Leu234=)
n.724G>T
7g.152648783C>GCA458895278XRCC2c.534G>C (p.Leu178=)
c.702G>C (p.Leu234=)
n.724G>C
 ClinVar dbSNP gnomAD v4
7g.152648783C>TCA458895279XRCC2c.534G>A (p.Leu178=)
c.702G>A (p.Leu234=)
n.724G>A
 ClinVar dbSNP gnomAD v4
7g.152648784A>CCA370198135XRCC2c.533T>G (p.Leu178Arg)
c.701T>G (p.Leu234Arg)
n.723T>G
7g.152648784A>GCA370198133XRCC2c.533T>C (p.Leu178Pro)
c.701T>C (p.Leu234Pro)
n.723T>C
 ClinVar
7g.152648784A>TCA370198134XRCC2c.533T>A (p.Leu178Gln)
c.701T>A (p.Leu234Gln)
n.723T>A
7g.152648785G>ACA458895280XRCC2c.532C>T (p.Leu178=)
c.700C>T (p.Leu234=)
n.722C>T
7g.152648785G>CCA370198136XRCC2c.532C>G (p.Leu178Val)
c.700C>G (p.Leu234Val)
n.722C>G
 dbSNP
7g.152648785G>TCA370198137XRCC2c.532C>A (p.Leu178Met)
c.700C>A (p.Leu234Met)
n.722C>A
7g.152648786T>ACA370198138XRCC2c.531A>T (p.Gln177His)
c.699A>T (p.Gln233His)
n.721A>T
7g.152648786T>CCA169486940XRCC2c.531A>G (p.Gln177=)
c.699A>G (p.Gln233=)
n.721A>G
 ClinVar dbSNP
7g.152648786T>GCA370198139XRCC2c.531A>C (p.Gln177His)
c.699A>C (p.Gln233His)
n.721A>C
7g.152648786T=CA1753246759XRCC2c.531A= (p.Gln177=)
c.699A= (p.Gln233=)
n.721A=
7g.152648787T>ACA169486941XRCC2c.530A>T (p.Gln177Leu)
c.698A>T (p.Gln233Leu)
n.720A>T
 ClinVar dbSNP gnomAD v4
7g.152648787T>CCA370198140XRCC2c.530A>G (p.Gln177Arg)
c.698A>G (p.Gln233Arg)
n.720A>G
7g.152648787T>GCA370198141XRCC2c.530A>C (p.Gln177Pro)
c.698A>C (p.Gln233Pro)
n.720A>C
7g.152648787T=CA1753246765XRCC2c.530A= (p.Gln177=)
c.698A= (p.Gln233=)
n.720A=
7g.152648788G>ACA370198142XRCC2c.529C>T (p.Gln177Ter)
c.697C>T (p.Gln233Ter)
n.719C>T
7g.152648788G>CCA370198143XRCC2c.529C>G (p.Gln177Glu)
c.697C>G (p.Gln233Glu)
n.719C>G
 dbSNP
7g.152648788G>TCA370198144XRCC2c.529C>A (p.Gln177Lys)
c.697C>A (p.Gln233Lys)
n.719C>A
7g.152648789C>ACA370198145XRCC2c.528G>T (p.Gln176His)
c.696G>T (p.Gln232His)
n.718G>T
7g.152648789C>GCA370198146XRCC2c.528G>C (p.Gln176His)
c.696G>C (p.Gln232His)
n.718G>C
7g.152648789C>TCA458895281XRCC2c.528G>A (p.Gln176=)
c.696G>A (p.Gln232=)
n.718G>A
7g.152648790T>ACA370198149XRCC2c.527A>T (p.Gln176Leu)
c.695A>T (p.Gln232Leu)
n.717A>T
7g.152648790T>CCA370198148XRCC2c.527A>G (p.Gln176Arg)
c.695A>G (p.Gln232Arg)
n.717A>G
7g.152648790T>GCA370198147XRCC2c.527A>C (p.Gln176Pro)
c.695A>C (p.Gln232Pro)
n.717A>C
7g.152648791G>ACA370198150XRCC2c.526C>T (p.Gln176Ter)
c.694C>T (p.Gln232Ter)
n.716C>T
 ClinVar dbSNP
7g.152648791G>CCA370198151XRCC2c.526C>G (p.Gln176Glu)
c.694C>G (p.Gln232Glu)
n.716C>G
7g.152648791G>TCA370198152XRCC2c.526C>A (p.Gln176Lys)
c.694C>A (p.Gln232Lys)
n.716C>A
7g.152648792C>ACA370198153XRCC2c.525G>T (p.Trp175Cys)
c.693G>T (p.Trp231Cys)
n.715G>T
 ClinVar dbSNP
7g.152648792C=CA1753246770XRCC2c.525G= (p.Trp175=)
c.693G= (p.Trp231=)
n.715G=
7g.152648792C>GCA370198154XRCC2c.525G>C (p.Trp175Cys)
c.693G>C (p.Trp231Cys)
n.715G>C
 ClinVar
7g.152648792C>TCA370198155XRCC2c.525G>A (p.Trp175Ter)
c.693G>A (p.Trp231Ter)
n.715G>A
 dbSNP
7g.152648793C>ACA370198156XRCC2c.524G>T (p.Trp175Leu)
c.692G>T (p.Trp231Leu)
n.714G>T
7g.152648793C>GCA370198158XRCC2c.524G>C (p.Trp175Ser)
c.692G>C (p.Trp231Ser)
n.714G>C
7g.152648793C>TCA370198157XRCC2c.524G>A (p.Trp175Ter)
c.692G>A (p.Trp231Ter)
n.714G>A
7g.152648794A>CCA370198159XRCC2c.523T>G (p.Trp175Gly)
c.691T>G (p.Trp231Gly)
n.713T>G
7g.152648794A>GCA370198160XRCC2c.523T>C (p.Trp175Arg)
c.691T>C (p.Trp231Arg)
n.713T>C
 ClinVar
7g.152648794A>TCA370198161XRCC2c.523T>A (p.Trp175Arg)
c.691T>A (p.Trp231Arg)
n.713T>A
7g.152648795T>ACA458895284XRCC2c.522A>T (p.Ala174=)
c.690A>T (p.Ala230=)
n.712A>T
7g.152648795T>CCA458895283XRCC2c.522A>G (p.Ala174=)
c.690A>G (p.Ala230=)
n.712A>G
 ClinVar dbSNP gnomAD v4 COSMIC
7g.152648795T>GCA458895282XRCC2c.522A>C (p.Ala174=)
c.690A>C (p.Ala230=)
n.712A>C
7g.152648796G>ACA370198162XRCC2c.521C>T (p.Ala174Val)
c.689C>T (p.Ala230Val)
n.711C>T
 ClinVar gnomAD v4
7g.152648796G>CCA370198163XRCC2c.521C>G (p.Ala174Gly)
c.689C>G (p.Ala230Gly)
n.711C>G
7g.152648796G>TCA370198164XRCC2c.521C>A (p.Ala174Glu)
c.689C>A (p.Ala230Glu)
n.711C>A
7g.152648797C>ACA370198167XRCC2c.520G>T (p.Ala174Ser)
c.688G>T (p.Ala230Ser)
n.710G>T
7g.152648797C>GCA370198165XRCC2c.520G>C (p.Ala174Pro)
c.688G>C (p.Ala230Pro)
n.710G>C
7g.152648797C>TCA370198166XRCC2c.520G>A (p.Ala174Thr)
c.688G>A (p.Ala230Thr)
n.710G>A
7g.152648798C>ACA370198168XRCC2c.519G>T (p.Lys173Asn)
c.687G>T (p.Lys229Asn)
n.709G>T
7g.152648798C=CA1753246776XRCC2c.519G= (p.Lys173=)
c.687G= (p.Lys229=)
n.709G=
7g.152648798C>GCA370198169XRCC2c.519G>C (p.Lys173Asn)
c.687G>C (p.Lys229Asn)
n.709G>C
 dbSNP gnomAD v3 gnomAD v4
7g.152648798C>TCA458895285XRCC2c.519G>A (p.Lys173=)
c.687G>A (p.Lys229=)
n.709G>A
 gnomAD v4
7g.152648799T>ACA370198170XRCC2c.518A>T (p.Lys173Met)
c.686A>T (p.Lys229Met)
n.708A>T
7g.152648799T>CCA370198171XRCC2c.518A>G (p.Lys173Arg)
c.686A>G (p.Lys229Arg)
n.708A>G
7g.152648799T>GCA370198172XRCC2c.518A>C (p.Lys173Thr)
c.686A>C (p.Lys229Thr)
n.708A>C
7g.152648800T>ACA370198173XRCC2c.517A>T (p.Lys173Ter)
c.685A>T (p.Lys229Ter)
n.707A>T
7g.152648800T>CCA370198175XRCC2c.517A>G (p.Lys173Glu)
c.685A>G (p.Lys229Glu)
n.707A>G
 ClinVar gnomAD v4
7g.152648800T>GCA370198174XRCC2c.517A>C (p.Lys173Gln)
c.685A>C (p.Lys229Gln)
n.707A>C
7g.152648801A>CCA370198176XRCC2c.516T>G (p.Cys172Trp)
c.684T>G (p.Cys228Trp)
n.706T>G
7g.152648801A>GCA458895286XRCC2c.516T>C (p.Cys172=)
c.684T>C (p.Cys228=)
n.706T>C
 COSMIC
7g.152648801A>TCA370198177XRCC2c.516T>A (p.Cys172Ter)
c.684T>A (p.Cys228Ter)
n.706T>A
7g.152648802C>ACA370198178XRCC2c.515G>T (p.Cys172Phe)
c.683G>T (p.Cys228Phe)
n.705G>T
7g.152648802C>GCA370198179XRCC2c.515G>C (p.Cys172Ser)
c.683G>C (p.Cys228Ser)
n.705G>C
 gnomAD v4
7g.152648802C>TCA370198180XRCC2c.515G>A (p.Cys172Tyr)
c.683G>A (p.Cys228Tyr)
n.705G>A
 dbSNP
7g.152648803A=CA1753246780XRCC2c.514T= (p.Cys172=)
c.682T= (p.Cys228=)
n.704T=
7g.152648803A>CCA370198181XRCC2c.514T>G (p.Cys172Gly)
c.682T>G (p.Cys228Gly)
n.704T>G
7g.152648803A>GCA4582309XRCC2c.514T>C (p.Cys172Arg)
c.682T>C (p.Cys228Arg)
n.704T>C
 ClinVar dbSNP ExAC gnomAD v4
7g.152648803A>TCA370198182XRCC2c.514T>A (p.Cys172Ser)
c.682T>A (p.Cys228Ser)
n.704T>A
7g.152648806_152648807dupCA2685735767XRCC2c.513_514dup (p.Cys172SerfsTer9)
c.681_682dup (p.Cys228SerfsTer9)
n.703_704dup
 gnomAD v4
7g.152648804G>ACA458895287XRCC2c.513C>T (p.Leu171=)
c.681C>T (p.Leu227=)
n.703C>T
 ClinVar dbSNP gnomAD v4
7g.152648804G>CCA458895288XRCC2c.513C>G (p.Leu171=)
c.681C>G (p.Leu227=)
n.703C>G
 dbSNP
7g.152648804G=CA1753246783XRCC2c.513C= (p.Leu171=)
c.681C= (p.Leu227=)
n.703C=
7g.152648804G>TCA458895289XRCC2c.513C>A (p.Leu171=)
c.681C>A (p.Leu227=)
n.703C>A
7g.152648805A=CA1753246788XRCC2c.512T= (p.Leu171=)
c.680T= (p.Leu227=)
n.702T=
7g.152648805A>CCA370198183XRCC2c.512T>G (p.Leu171Arg)
c.680T>G (p.Leu227Arg)
n.702T>G
7g.152648805A>GCA4582310XRCC2c.512T>C (p.Leu171Pro)
c.680T>C (p.Leu227Pro)
n.702T>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648805A>TCA370198184XRCC2c.512T>A (p.Leu171His)
c.680T>A (p.Leu227His)
n.702T>A
7g.152648806G>ACA370198185XRCC2c.511C>T (p.Leu171Phe)
c.679C>T (p.Leu227Phe)
n.701C>T
 dbSNP gnomAD v2
7g.152648806G>CCA370198187XRCC2c.511C>G (p.Leu171Val)
c.679C>G (p.Leu227Val)
n.701C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648806G=CA1753246792XRCC2c.511C= (p.Leu171=)
c.679C= (p.Leu227=)
n.701C=
7g.152648806G>TCA370198186XRCC2c.511C>A (p.Leu171Ile)
c.679C>A (p.Leu227Ile)
n.701C>A
7g.152648807A=CA1753246799XRCC2c.510T= (p.Tyr170=)
c.678T= (p.Tyr226=)
n.700T=
7g.152648807A>CCA300479XRCC2c.510T>G (p.Tyr170Ter)
c.678T>G (p.Tyr226Ter)
n.700T>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648807A>GCA4582311XRCC2c.510T>C (p.Tyr170=)
c.678T>C (p.Tyr226=)
n.700T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648807A>TCA370198188XRCC2c.510T>A (p.Tyr170Ter)
c.678T>A (p.Tyr226Ter)
n.700T>A
7g.152648808T>ACA370198189XRCC2c.509A>T (p.Tyr170Phe)
c.677A>T (p.Tyr226Phe)
n.699A>T
 ClinVar
7g.152648808T>CCA370198190XRCC2c.509A>G (p.Tyr170Cys)
c.677A>G (p.Tyr226Cys)
n.699A>G
7g.152648808T>GCA370198191XRCC2c.509A>C (p.Tyr170Ser)
c.677A>C (p.Tyr226Ser)
n.699A>C
7g.152648808dupCA915945587XRCC2c.509dup (p.Tyr170Ter)
c.677dup (p.Tyr226Ter)
n.699dup
 ClinVar dbSNP gnomAD v4
7g.152648809A>CCA370198192XRCC2c.508T>G (p.Tyr170Asp)
c.676T>G (p.Tyr226Asp)
n.698T>G
7g.152648809A>GCA370198193XRCC2c.508T>C (p.Tyr170His)
c.676T>C (p.Tyr226His)
n.698T>C
7g.152648809A>TCA370198194XRCC2c.508T>A (p.Tyr170Asn)
c.676T>A (p.Tyr226Asn)
n.698T>A
7g.152648810A>CCA458895292XRCC2c.507T>G (p.Pro169=)
c.675T>G (p.Pro225=)
n.697T>G
 ClinVar
7g.152648810A>GCA458895291XRCC2c.507T>C (p.Pro169=)
c.675T>C (p.Pro225=)
n.697T>C
7g.152648810A>TCA458895290XRCC2c.507T>A (p.Pro169=)
c.675T>A (p.Pro225=)
n.697T>A
7g.152648811G>ACA370198195XRCC2c.506C>T (p.Pro169Leu)
c.674C>T (p.Pro225Leu)
n.696C>T
 ClinVar
7g.152648811G>CCA370198196XRCC2c.506C>G (p.Pro169Arg)
c.674C>G (p.Pro225Arg)
n.696C>G
7g.152648811G>TCA370198197XRCC2c.506C>A (p.Pro169His)
c.674C>A (p.Pro225His)
n.696C>A
7g.152648812G>ACA169486942XRCC2c.505C>T (p.Pro169Ser)
c.673C>T (p.Pro225Ser)
n.695C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648812G>CCA370198198XRCC2c.505C>G (p.Pro169Ala)
c.673C>G (p.Pro225Ala)
n.695C>G
 dbSNP
7g.152648812G=CA1753246807XRCC2c.505C= (p.Pro169=)
c.673C= (p.Pro225=)
n.695C=
7g.152648812G>TCA370198199XRCC2c.505C>A (p.Pro169Thr)
c.673C>A (p.Pro225Thr)
n.695C>A
7g.152648813T>ACA370198200XRCC2c.504A>T (p.Arg168Ser)
c.672A>T (p.Arg224Ser)
n.694A>T
7g.152648813T>CCA458895293XRCC2c.504A>G (p.Arg168=)
c.672A>G (p.Arg224=)
n.694A>G
7g.152648813T>GCA370198201XRCC2c.504A>C (p.Arg168Ser)
c.672A>C (p.Arg224Ser)
n.694A>C
 ClinVar
7g.152648814C>ACA370198202XRCC2c.503G>T (p.Arg168Ile)
c.671G>T (p.Arg224Ile)
n.693G>T
 gnomAD v4
7g.152648814C=CA1753246810XRCC2c.503G= (p.Arg168=)
c.671G= (p.Arg224=)
n.693G=
7g.152648814C>GCA370198203XRCC2c.503G>C (p.Arg168Thr)
c.671G>C (p.Arg224Thr)
n.693G>C
 ClinVar dbSNP
7g.152648814C>TCA370198204XRCC2c.503G>A (p.Arg168Lys)
c.671G>A (p.Arg224Lys)
n.693G>A
 ClinVar dbSNP
7g.152648815T>ACA370198205XRCC2c.502A>T (p.Arg168Ter)
c.670A>T (p.Arg224Ter)
n.692A>T
7g.152648815T>CCA370198206XRCC2c.502A>G (p.Arg168Gly)
c.670A>G (p.Arg224Gly)
n.692A>G
7g.152648815T>GCA458895294XRCC2c.502A>C (p.Arg168=)
c.670A>C (p.Arg224=)
n.692A>C
7g.152648816_152648817dupCA579080839XRCC2c.501_502dup (p.Arg168ThrfsTer13)
c.669_670dup (p.Arg224ThrfsTer13)
n.691_692dup
 dbSNP gnomAD v2 gnomAD v4
7g.152648816G>ACA4582312XRCC2c.501C>T (p.Tyr167=)
c.669C>T (p.Tyr223=)
n.691C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648816G>CCA370198207XRCC2c.501C>G (p.Tyr167Ter)
c.669C>G (p.Tyr223Ter)
n.691C>G
 dbSNP
7g.152648816G=CA1753246816XRCC2c.501C= (p.Tyr167=)
c.669C= (p.Tyr223=)
n.691C=
7g.152648816G>TCA370198208XRCC2c.501C>A (p.Tyr167Ter)
c.669C>A (p.Tyr223Ter)
n.691C>A
7g.152648817T>ACA370198209XRCC2c.500A>T (p.Tyr167Phe)
c.668A>T (p.Tyr223Phe)
n.690A>T
7g.152648817T>CCA370198210XRCC2c.500A>G (p.Tyr167Cys)
c.668A>G (p.Tyr223Cys)
n.690A>G
 ClinVar gnomAD v4
7g.152648817T>GCA370198211XRCC2c.500A>C (p.Tyr167Ser)
c.668A>C (p.Tyr223Ser)
n.690A>C
7g.152648818A=CA1753246823XRCC2c.499T= (p.Tyr167=)
c.667T= (p.Tyr223=)
n.689T=
7g.152648818A>CCA370198213XRCC2c.499T>G (p.Tyr167Asp)
c.667T>G (p.Tyr223Asp)
n.689T>G
 ClinVar
7g.152648818A>GCA288145XRCC2c.499T>C (p.Tyr167His)
c.667T>C (p.Tyr223His)
n.689T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648818A>TCA370198212XRCC2c.499T>A (p.Tyr167Asn)
c.667T>A (p.Tyr223Asn)
n.689T>A
 ClinVar
7g.152648819G>ACA458895312XRCC2c.498C>T (p.Asp166=)
c.666C>T (p.Asp222=)
n.688C>T
7g.152648819G>CCA370198214XRCC2c.498C>G (p.Asp166Glu)
c.666C>G (p.Asp222Glu)
n.688C>G
 gnomAD v4
7g.152648819G>TCA370198215XRCC2c.498C>A (p.Asp166Glu)
c.666C>A (p.Asp222Glu)
n.688C>A
7g.152648820T>ACA370198216XRCC2c.497A>T (p.Asp166Val)
c.665A>T (p.Asp222Val)
n.687A>T
7g.152648820T>CCA370198217XRCC2c.497A>G (p.Asp166Gly)
c.665A>G (p.Asp222Gly)
n.687A>G
7g.152648820T>GCA370198218XRCC2c.497A>C (p.Asp166Ala)
c.665A>C (p.Asp222Ala)
n.687A>C
7g.152648821C>ACA370198219XRCC2c.496G>T (p.Asp166Tyr)
c.664G>T (p.Asp222Tyr)
n.686G>T
 ClinVar
7g.152648821C>GCA370198220XRCC2c.496G>C (p.Asp166His)
c.664G>C (p.Asp222His)
n.686G>C
7g.152648821C>TCA370198221XRCC2c.496G>A (p.Asp166Asn)
c.664G>A (p.Asp222Asn)
n.686G>A
7g.152648822T>ACA458895316XRCC2c.495A>T (p.Ile165=)
c.663A>T (p.Ile221=)
n.685A>T
7g.152648822T>CCA370198222XRCC2c.495A>G (p.Ile165Met)
c.663A>G (p.Ile221Met)
n.685A>G
 gnomAD v4
7g.152648822T>GCA458895317XRCC2c.495A>C (p.Ile165=)
c.663A>C (p.Ile221=)
n.685A>C
 dbSNP gnomAD v2 gnomAD v4
7g.152648822T=CA1753246832XRCC2c.495A= (p.Ile165=)
c.663A= (p.Ile221=)
n.685A=
7g.152648823A=CA1753246837XRCC2c.494T= (p.Ile165=)
c.662T= (p.Ile221=)
n.684T=
7g.152648823A>CCA370198223XRCC2c.494T>G (p.Ile165Arg)
c.662T>G (p.Ile221Arg)
n.684T>G
7g.152648823A>GCA4582313XRCC2c.494T>C (p.Ile165Thr)
c.662T>C (p.Ile221Thr)
n.684T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648823A>TCA370198224XRCC2c.494T>A (p.Ile165Lys)
c.662T>A (p.Ile221Lys)
n.684T>A
7g.152648824T>ACA370198226XRCC2c.493A>T (p.Ile165Leu)
c.661A>T (p.Ile221Leu)
n.683A>T
7g.152648824T>CCA169486943XRCC2c.493A>G (p.Ile165Val)
c.661A>G (p.Ile221Val)
n.683A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648824T>GCA370198225XRCC2c.493A>C (p.Ile165Leu)
c.661A>C (p.Ile221Leu)
n.683A>C
7g.152648824T=CA1753246842XRCC2c.493A= (p.Ile165=)
c.661A= (p.Ile221=)
n.683A=
7g.152648825G>ACA458895319XRCC2c.492C>T (p.Asp164=)
c.660C>T (p.Asp220=)
n.682C>T
 ClinVar dbSNP gnomAD v4
7g.152648825G>CCA370198227XRCC2c.492C>G (p.Asp164Glu)
c.660C>G (p.Asp220Glu)
n.682C>G
7g.152648825G=CA1753246845XRCC2c.492C= (p.Asp164=)
c.660C= (p.Asp220=)
n.682C=
7g.152648825G>TCA370198228XRCC2c.492C>A (p.Asp164Glu)
c.660C>A (p.Asp220Glu)
n.682C>A
7g.152648826T>ACA4582314XRCC2c.491A>T (p.Asp164Val)
c.659A>T (p.Asp220Val)
n.681A>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648826T>CCA370198229XRCC2c.491A>G (p.Asp164Gly)
c.659A>G (p.Asp220Gly)
n.681A>G
 ClinVar
7g.152648826T>GCA370198230XRCC2c.491A>C (p.Asp164Ala)
c.659A>C (p.Asp220Ala)
n.681A>C
7g.152648826T=CA1753246849XRCC2c.491A= (p.Asp164=)
c.659A= (p.Asp220=)
n.681A=
7g.152648827C>ACA370198233XRCC2c.490G>T (p.Asp164Tyr)
c.658G>T (p.Asp220Tyr)
n.680G>T
7g.152648827C=CA1753246854XRCC2c.490G= (p.Asp164=)
c.658G= (p.Asp220=)
n.680G=
7g.152648827C>GCA370198231XRCC2c.490G>C (p.Asp164His)
c.658G>C (p.Asp220His)
n.680G>C
 dbSNP gnomAD v2 gnomAD v4
7g.152648827C>TCA370198232XRCC2c.490G>A (p.Asp164Asn)
c.658G>A (p.Asp220Asn)
n.680G>A
 ClinVar dbSNP
7g.152648828C>ACA458895321XRCC2c.489G>T (p.Val163=)
c.657G>T (p.Val219=)
n.679G>T
7g.152648828C>GCA458895322XRCC2c.489G>C (p.Val163=)
c.657G>C (p.Val219=)
n.679G>C
7g.152648828C>TCA458895323XRCC2c.489G>A (p.Val163=)
c.657G>A (p.Val219=)
n.679G>A
7g.152648829A>CCA370198234XRCC2c.488T>G (p.Val163Gly)
c.656T>G (p.Val219Gly)
n.678T>G
7g.152648829A>GCA370198235XRCC2c.488T>C (p.Val163Ala)
c.656T>C (p.Val219Ala)
n.678T>C
7g.152648829A>TCA370198236XRCC2c.488T>A (p.Val163Glu)
c.656T>A (p.Val219Glu)
n.678T>A
7g.152648830C>ACA370198237XRCC2c.487G>T (p.Val163Leu)
c.655G>T (p.Val219Leu)
n.677G>T
7g.152648830C=CA1753246858XRCC2c.487G= (p.Val163=)
c.655G= (p.Val219=)
n.677G=
7g.152648830C>GCA370198238XRCC2c.487G>C (p.Val163Leu)
c.655G>C (p.Val219Leu)
n.677G>C
7g.152648830C>TCA4582315XRCC2c.487G>A (p.Val163Met)
c.655G>A (p.Val219Met)
n.677G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648831A>CCA370198239XRCC2c.486T>G (p.Asp162Glu)
c.654T>G (p.Asp218Glu)
n.676T>G
7g.152648831A>GCA458895325XRCC2c.486T>C (p.Asp162=)
c.654T>C (p.Asp218=)
n.676T>C
 ClinVar dbSNP gnomAD v4
7g.152648831A>TCA370198240XRCC2c.486T>A (p.Asp162Glu)
c.654T>A (p.Asp218Glu)
n.676T>A
7g.152648832T>ACA370198241XRCC2c.485A>T (p.Asp162Val)
c.653A>T (p.Asp218Val)
n.675A>T
7g.152648832T>CCA370198243XRCC2c.485A>G (p.Asp162Gly)
c.653A>G (p.Asp218Gly)
n.675A>G
 ClinVar dbSNP gnomAD v4
7g.152648832T>GCA370198242XRCC2c.485A>C (p.Asp162Ala)
c.653A>C (p.Asp218Ala)
n.675A>C
7g.152648832_152648834delinsTCACA1753246865XRCC2c.483_485delinsTGA (p.Cys161=)
c.651_653delinsTGA (p.Cys217=)
n.673_675delinsTGA
7g.152648833C>ACA370198244XRCC2c.484G>T (p.Asp162Tyr)
c.652G>T (p.Asp218Tyr)
n.674G>T
7g.152648833C=CA1753246872XRCC2c.484G= (p.Asp162=)
c.652G= (p.Asp218=)
n.674G=
7g.152648833C>GCA370198245XRCC2c.484G>C (p.Asp162His)
c.652G>C (p.Asp218His)
n.674G>C
7g.152648833C>TCA370198246XRCC2c.484G>A (p.Asp162Asn)
c.652G>A (p.Asp218Asn)
n.674G>A
 dbSNP gnomAD v2 gnomAD v4
7g.152648837_152648838delCA16618428XRCC2c.483_484del (p.Cys161Ter)
c.651_652del (p.Cys217Ter)
n.673_674del
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648834A=CA1753246876XRCC2c.483T= (p.Cys161=)
c.651T= (p.Cys217=)
n.673T=
7g.152648834A>CCA370198248XRCC2c.483T>G (p.Cys161Trp)
c.651T>G (p.Cys217Trp)
n.673T>G
7g.152648834A>GCA458895327XRCC2c.483T>C (p.Cys161=)
c.651T>C (p.Cys217=)
n.673T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648834A>TCA370198247XRCC2c.483T>A (p.Cys161Ter)
c.651T>A (p.Cys217Ter)
n.673T>A
7g.152648838_152648839insACCAAACACACCCAACACACA2778474372XRCC2c.483_484insTGGGTGTGTTTGGTTGTGT (p.Asp162TrpfsTer7)
c.651_652insTGGGTGTGTTTGGTTGTGT (p.Asp218TrpfsTer7)
n.673_674insTGGGTGTGTTTGGTTGTGT
7g.152648835C>ACA370198249XRCC2c.482G>T (p.Cys161Phe)
c.650G>T (p.Cys217Phe)
n.672G>T
7g.152648835C=CA1753246879XRCC2c.482G= (p.Cys161=)
c.650G= (p.Cys217=)
n.672G=
7g.152648835C>GCA370198250XRCC2c.482G>C (p.Cys161Ser)
c.650G>C (p.Cys217Ser)
n.672G>C
 dbSNP
7g.152648835C>TCA10584276XRCC2c.482G>A (p.Cys161Tyr)
c.650G>A (p.Cys217Tyr)
n.672G>A
 ClinVar dbSNP
7g.152648836A=CA1753246882XRCC2c.481T= (p.Cys161=)
c.649T= (p.Cys217=)
n.671T=
7g.152648836A>CCA370198251XRCC2c.481T>G (p.Cys161Gly)
c.649T>G (p.Cys217Gly)
n.671T>G
7g.152648836A>GCA370198252XRCC2c.481T>C (p.Cys161Arg)
c.649T>C (p.Cys217Arg)
n.671T>C
 dbSNP
7g.152648836A>TCA370198253XRCC2c.481T>A (p.Cys161Ser)
c.649T>A (p.Cys217Ser)
n.671T>A
 gnomAD v4
7g.152648837C>ACA458895330XRCC2c.480G>T (p.Leu160=)
c.648G>T (p.Leu216=)
n.670G>T
 ClinVar
7g.152648837C>GCA458895331XRCC2c.480G>C (p.Leu160=)
c.648G>C (p.Leu216=)
n.670G>C
7g.152648837C>TCA458895332XRCC2c.480G>A (p.Leu160=)
c.648G>A (p.Leu216=)
n.670G>A
 ClinVar gnomAD v4
7g.152648837_152648847delinsCAGTCGTCGAGCA1753246884XRCC2c.470_480delinsCTCGACGACTG (p.Ser157=)
c.638_648delinsCTCGACGACTG (p.Ser213=)
n.660_670delinsCTCGACGACTG
7g.152648838A=CA1753246887XRCC2c.479T= (p.Leu160=)
c.647T= (p.Leu216=)
n.669T=
7g.152648838A>CCA370198254XRCC2c.479T>G (p.Leu160Arg)
c.647T>G (p.Leu216Arg)
n.669T>G
7g.152648838A>GCA370198255XRCC2c.479T>C (p.Leu160Pro)
c.647T>C (p.Leu216Pro)
n.669T>C
 ClinVar dbSNP gnomAD v4
7g.152648838A>TCA370198256XRCC2c.479T>A (p.Leu160Gln)
c.647T>A (p.Leu216Gln)
n.669T>A
7g.152648840_152648849delCA579080840XRCC2c.470_479del (p.Ser157CysfsTer6)
c.638_647del (p.Ser213CysfsTer6)
n.660_669del
 dbSNP gnomAD v2 gnomAD v4
7g.152648839G>ACA458895333XRCC2c.478C>T (p.Leu160=)
c.646C>T (p.Leu216=)
n.668C>T
7g.152648839G>CCA370198257XRCC2c.478C>G (p.Leu160Val)
c.646C>G (p.Leu216Val)
n.668C>G
 dbSNP
7g.152648839G>TCA370198258XRCC2c.478C>A (p.Leu160Met)
c.646C>A (p.Leu216Met)
n.668C>A
7g.152648840T>ACA458895335XRCC2c.477A>T (p.Arg159=)
c.645A>T (p.Arg215=)
n.667A>T
7g.152648840T>CCA458895336XRCC2c.477A>G (p.Arg159=)
c.645A>G (p.Arg215=)
n.667A>G
 gnomAD v4
7g.152648840T>GCA458895337XRCC2c.477A>C (p.Arg159=)
c.645A>C (p.Arg215=)
n.667A>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648840T=CA1753246889XRCC2c.477A= (p.Arg159=)
c.645A= (p.Arg215=)
n.667A=
7g.152648841C>ACA370198260XRCC2c.476G>T (p.Arg159Leu)
c.644G>T (p.Arg215Leu)
n.666G>T
 gnomAD v4
7g.152648841C=CA1753246892XRCC2c.476G= (p.Arg159=)
c.644G= (p.Arg215=)
n.666G=
7g.152648841C>GCA370198259XRCC2c.476G>C (p.Arg159Pro)
c.644G>C (p.Arg215Pro)
n.666G>C
7g.152648841C>TCA4582316XRCC2c.476G>A (p.Arg159Gln)
c.644G>A (p.Arg215Gln)
n.666G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched