Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.152648679_152648731delCA2685735766XRCC2c.586_638del (p.Gln196PhefsTer9)
c.754_806del (p.Gln252PhefsTer9)
n.776_828del
 gnomAD v4
7g.152648698_152648709delinsTACTTTTTAAACCA1753246565XRCC2c.608_619delinsGTTTAAAAAGTA (p.Cys203=)
c.776_787delinsGTTTAAAAAGTA (p.Cys259=)
n.798_809delinsGTTTAAAAAGTA
7g.152648699_152648709delinsGTTTACA288149XRCC2c.608_618delinsTAAAC (p.Cys203_Ser206delinsLeuAsn)
c.776_786delinsTAAAC (p.Cys259_Ser262delinsLeuAsn)
n.798_808delinsTAAAC
 ClinVar dbSNP
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
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
 ClinVar
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
 ClinVar
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.152648773dupCA2825001567XRCC2c.544dup (p.Arg182LysfsTer9)
c.712dup (p.Arg238LysfsTer9)
n.734dup
 ClinVar
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
 ClinVar 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

Number of alleles fetched