Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.43551605A=CA2337551269XRCC1c.1165T= (p.Cys389=)
c.1072T= (p.Cys358=)
c.775T=
19g.43551605A>CCA406203304XRCC1c.1165T>G (p.Cys389Gly)
c.1072T>G (p.Cys358Gly)
c.775T>G
19g.43551605A>GCA308773369XRCC1c.1165T>C (p.Cys389Arg)
c.1072T>C (p.Cys358Arg)
c.775T>C
 dbSNP gnomAD v4
19g.43551605A>TCA406203305XRCC1c.1165T>A (p.Cys389Ser)
c.1072T>A (p.Cys358Ser)
c.775T>A
 dbSNP
19g.43551606G>ACA507741025XRCC1c.1164C>T (p.Asp388=)
c.1071C>T (p.Asp357=)
c.774C>T
 dbSNP
19g.43551606G>CCA406203308XRCC1c.1164C>G (p.Asp388Glu)
c.1071C>G (p.Asp357Glu)
c.774C>G
 dbSNP
19g.43551606G>TCA406203310XRCC1c.1164C>A (p.Asp388Glu)
c.1071C>A (p.Asp357Glu)
c.774C>A
19g.43551607T>ACA406203314XRCC1c.1163A>T (p.Asp388Val)
c.1070A>T (p.Asp357Val)
c.773A>T
19g.43551607T>CCA406203318XRCC1c.1163A>G (p.Asp388Gly)
c.1070A>G (p.Asp357Gly)
c.773A>G
19g.43551607T>GCA406203315XRCC1c.1163A>C (p.Asp388Ala)
c.1070A>C (p.Asp357Ala)
c.773A>C
19g.43551607T=CA2337551270XRCC1c.1163A= (p.Asp388=)
c.1070A= (p.Asp357=)
c.773A=
19g.43551608C>ACA406203320XRCC1c.1162G>T (p.Asp388Tyr)
c.1069G>T (p.Asp357Tyr)
c.772G>T
19g.43551608C=CA2337551271XRCC1c.1162G= (p.Asp388=)
c.1069G= (p.Asp357=)
c.772G=
19g.43551608C>GCA406203322XRCC1c.1162G>C (p.Asp388His)
c.1069G>C (p.Asp357His)
c.772G>C
 dbSNP
19g.43551608C>TCA308773372XRCC1c.1162G>A (p.Asp388Asn)
c.1069G>A (p.Asp357Asn)
c.772G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.43551609dupCA920114762XRCC1c.1162dup (p.Asp388GlyfsTer24)
c.1069dup (p.Asp357GlyfsTer24)
c.772dup
 dbSNP
19g.43551609C>ACA507741026XRCC1c.1161G>T (p.Leu387=)
c.1068G>T (p.Leu356=)
c.771G>T
 dbSNP
19g.43551609C=CA2337551272XRCC1c.1161G= (p.Leu387=)
c.1068G= (p.Leu356=)
c.771G=
19g.43551609C>GCA507741027XRCC1c.1161G>C (p.Leu387=)
c.1068G>C (p.Leu356=)
c.771G>C
 dbSNP
19g.43551609C>TCA308773375XRCC1c.1161G>A (p.Leu387=)
c.1068G>A (p.Leu356=)
c.771G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.43551610A>CCA406203331XRCC1c.1160T>G (p.Leu387Arg)
c.1067T>G (p.Leu356Arg)
c.770T>G
 dbSNP
19g.43551610A>GCA406203334XRCC1c.1160T>C (p.Leu387Pro)
c.1067T>C (p.Leu356Pro)
c.770T>C
 dbSNP gnomAD v4
19g.43551610A>TCA406203335XRCC1c.1160T>A (p.Leu387Gln)
c.1067T>A (p.Leu356Gln)
c.770T>A
 dbSNP
19g.43551611G>ACA507741028XRCC1c.1159C>T (p.Leu387=)
c.1066C>T (p.Leu356=)
c.769C>T
 dbSNP
19g.43551611G>CCA9488528XRCC1c.1159C>G (p.Leu387Val)
c.1066C>G (p.Leu356Val)
c.769C>G
 dbSNP ExAC
19g.43551611G=CA2337551273XRCC1c.1159C= (p.Leu387=)
c.1066C= (p.Leu356=)
c.769C=
19g.43551611G>TCA406203336XRCC1c.1159C>A (p.Leu387Met)
c.1066C>A (p.Leu356Met)
c.769C>A
 dbSNP
19g.43551612C>ACA507741029XRCC1c.1158G>T (p.Val386=)
c.1065G>T (p.Val355=)
c.768G>T
 dbSNP
19g.43551612C>GCA507741030XRCC1c.1158G>C (p.Val386=)
c.1065G>C (p.Val355=)
c.768G>C
 dbSNP
19g.43551612C>TCA507741031XRCC1c.1158G>A (p.Val386=)
c.1065G>A (p.Val355=)
c.768G>A
 dbSNP COSMIC
19g.43551613A>CCA406203337XRCC1c.1157T>G (p.Val386Gly)
c.1064T>G (p.Val355Gly)
c.767T>G
19g.43551613A>GCA406203339XRCC1c.1157T>C (p.Val386Ala)
c.1064T>C (p.Val355Ala)
c.767T>C
19g.43551613A>TCA406203340XRCC1c.1157T>A (p.Val386Glu)
c.1064T>A (p.Val355Glu)
c.767T>A
 dbSNP
19g.43551614C>ACA406203344XRCC1c.1156G>T (p.Val386Leu)
c.1063G>T (p.Val355Leu)
c.766G>T
19g.43551614C>GCA406203341XRCC1c.1156G>C (p.Val386Leu)
c.1063G>C (p.Val355Leu)
c.766G>C
 dbSNP
19g.43551614C>TCA406203342XRCC1c.1156G>A (p.Val386Met)
c.1063G>A (p.Val355Met)
c.766G>A
 dbSNP
19g.43551615C>ACA406203346XRCC1c.1155G>T (p.Trp385Cys)
c.1062G>T (p.Trp354Cys)
c.765G>T
 dbSNP
19g.43551615C>GCA406203348XRCC1c.1155G>C (p.Trp385Cys)
c.1062G>C (p.Trp354Cys)
c.765G>C
 dbSNP
19g.43551615C>TCA406203350XRCC1c.1155G>A (p.Trp385Ter)
c.1062G>A (p.Trp354Ter)
c.765G>A
19g.43551616C>ACA406203352XRCC1c.1154G>T (p.Trp385Leu)
c.1061G>T (p.Trp354Leu)
c.764G>T
 dbSNP
19g.43551616C=CA2337551274XRCC1c.1154G= (p.Trp385=)
c.1061G= (p.Trp354=)
c.764G=
19g.43551616C>GCA406203355XRCC1c.1154G>C (p.Trp385Ser)
c.1061G>C (p.Trp354Ser)
c.764G>C
19g.43551616C>TCA9488529XRCC1c.1154G>A (p.Trp385Ter)
c.1061G>A (p.Trp354Ter)
c.764G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551617A=CA2337551275XRCC1c.1153T= (p.Trp385=)
c.1060T= (p.Trp354=)
c.763T=
19g.43551617A>CCA308773380XRCC1c.1153T>G (p.Trp385Gly)
c.1060T>G (p.Trp354Gly)
c.763T>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.43551617A>GCA406203366XRCC1c.1153T>C (p.Trp385Arg)
c.1060T>C (p.Trp354Arg)
c.763T>C
19g.43551617A>TCA406203363XRCC1c.1153T>A (p.Trp385Arg)
c.1060T>A (p.Trp354Arg)
c.763T>A
 dbSNP
19g.43551618C>ACA406203372XRCC1c.1152G>T (p.Glu384Asp)
c.1059G>T (p.Glu353Asp)
c.762G>T
 gnomAD v4
19g.43551618C=CA2337551276XRCC1c.1152G= (p.Glu384=)
c.1059G= (p.Glu353=)
c.762G=
19g.43551618C>GCA406203374XRCC1c.1152G>C (p.Glu384Asp)
c.1059G>C (p.Glu353Asp)
c.762G>C
19g.43551618C>TCA9488530XRCC1c.1152G>A (p.Glu384=)
c.1059G>A (p.Glu353=)
c.762G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.43551619T>ACA406203378XRCC1c.1151A>T (p.Glu384Val)
c.1058A>T (p.Glu353Val)
c.761A>T
 dbSNP
19g.43551619T>CCA406203379XRCC1c.1151A>G (p.Glu384Gly)
c.1058A>G (p.Glu353Gly)
c.761A>G
 dbSNP
19g.43551619T>GCA406203382XRCC1c.1151A>C (p.Glu384Ala)
c.1058A>C (p.Glu353Ala)
c.761A>C
19g.43551620C>ACA406203383XRCC1c.1150G>T (p.Glu384Ter)
c.1057G>T (p.Glu353Ter)
c.760G>T
 dbSNP
19g.43551620C=CA2337551277XRCC1c.1150G= (p.Glu384=)
c.1057G= (p.Glu353=)
c.760G=
19g.43551620C>GCA406203388XRCC1c.1150G>C (p.Glu384Gln)
c.1057G>C (p.Glu353Gln)
c.760G>C
 dbSNP
19g.43551620C>TCA406203386XRCC1c.1150G>A (p.Glu384Lys)
c.1057G>A (p.Glu353Lys)
c.760G>A
 dbSNP
19g.43551621C>ACA406203390XRCC1c.1149G>T (p.Lys383Asn)
c.1056G>T (p.Lys352Asn)
c.759G>T
19g.43551621C=CA2337551278XRCC1c.1149G= (p.Lys383=)
c.1056G= (p.Lys352=)
c.759G=
19g.43551621C>GCA406203391XRCC1c.1149G>C (p.Lys383Asn)
c.1056G>C (p.Lys352Asn)
c.759G>C
19g.43551621C>TCA507741032XRCC1c.1149G>A (p.Lys383=)
c.1056G>A (p.Lys352=)
c.759G>A
 dbSNP gnomAD v2 gnomAD v4
19g.43551622T>ACA406203394XRCC1c.1148A>T (p.Lys383Met)
c.1055A>T (p.Lys352Met)
c.758A>T
 dbSNP
19g.43551622T>CCA406203397XRCC1c.1148A>G (p.Lys383Arg)
c.1055A>G (p.Lys352Arg)
c.758A>G
 dbSNP
19g.43551622T>GCA406203399XRCC1c.1148A>C (p.Lys383Thr)
c.1055A>C (p.Lys352Thr)
c.758A>C
19g.43551623T>ACA406203403XRCC1c.1147A>T (p.Lys383Ter)
c.1054A>T (p.Lys352Ter)
c.757A>T
19g.43551623T>CCA406203406XRCC1c.1147A>G (p.Lys383Glu)
c.1054A>G (p.Lys352Glu)
c.757A>G
 dbSNP gnomAD v3 gnomAD v4
19g.43551623T>GCA406203408XRCC1c.1147A>C (p.Lys383Gln)
c.1054A>C (p.Lys352Gln)
c.757A>C
19g.43551623T=CA2337551279XRCC1c.1147A= (p.Lys383=)
c.1054A= (p.Lys352=)
c.757A=
19g.43551624A>CCA507741033XRCC1c.1146T>G (p.Arg382=)
c.1053T>G (p.Arg351=)
c.756T>G
19g.43551624A>GCA507741034XRCC1c.1146T>C (p.Arg382=)
c.1053T>C (p.Arg351=)
c.756T>C
19g.43551624A>TCA507741035XRCC1c.1146T>A (p.Arg382=)
c.1053T>A (p.Arg351=)
c.756T>A
19g.43551627_43551630delCA2736074758XRCC1c.1143_1146del (p.Lys383SerfsTer?)
c.1050_1053del (p.Lys352SerfsTer?)
c.753_756del
 dbSNP
19g.43551625C>ACA406203411XRCC1c.1145G>T (p.Arg382Leu)
c.1052G>T (p.Arg351Leu)
c.755G>T
19g.43551625C=CA2337551280XRCC1c.1145G= (p.Arg382=)
c.1052G= (p.Arg351=)
c.755G=
19g.43551625C>GCA406203414XRCC1c.1145G>C (p.Arg382Pro)
c.1052G>C (p.Arg351Pro)
c.755G>C
 dbSNP
19g.43551625C>TCA9488531XRCC1c.1145G>A (p.Arg382His)
c.1052G>A (p.Arg351His)
c.755G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551626G>ACA9488532XRCC1c.1144C>T (p.Arg382Cys)
c.1051C>T (p.Arg351Cys)
c.754C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.43551626G>CCA406203422XRCC1c.1144C>G (p.Arg382Gly)
c.1051C>G (p.Arg351Gly)
c.754C>G
 dbSNP
19g.43551626G=CA2337551281XRCC1c.1144C= (p.Arg382=)
c.1051C= (p.Arg351=)
c.754C=
19g.43551626G>TCA406203420XRCC1c.1144C>A (p.Arg382Ser)
c.1051C>A (p.Arg351Ser)
c.754C>A
 gnomAD v4
19g.43551627C>ACA507741036XRCC1c.1143G>T (p.Val381=)
c.1050G>T (p.Val350=)
c.753G>T
19g.43551627C=CA2337551282XRCC1c.1143G= (p.Val381=)
c.1050G= (p.Val350=)
c.753G=
19g.43551627C>GCA507741037XRCC1c.1143G>C (p.Val381=)
c.1050G>C (p.Val350=)
c.753G>C
 dbSNP gnomAD v4
19g.43551627C>TCA308773403XRCC1c.1143G>A (p.Val381=)
c.1050G>A (p.Val350=)
c.753G>A
 dbSNP gnomAD v4
19g.43551628A=CA2337551283XRCC1c.1142T= (p.Val381=)
c.1049T= (p.Val350=)
c.752T=
19g.43551628A>CCA406203425XRCC1c.1142T>G (p.Val381Gly)
c.1049T>G (p.Val350Gly)
c.752T>G
 dbSNP
19g.43551628A>GCA406203433XRCC1c.1142T>C (p.Val381Ala)
c.1049T>C (p.Val350Ala)
c.752T>C
 dbSNP
19g.43551628A>TCA9488533XRCC1c.1142T>A (p.Val381Glu)
c.1049T>A (p.Val350Glu)
c.752T>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551629C>ACA406203436XRCC1c.1141G>T (p.Val381Leu)
c.1048G>T (p.Val350Leu)
c.751G>T
 dbSNP
19g.43551629C=CA2337551284XRCC1c.1141G= (p.Val381=)
c.1048G= (p.Val350=)
c.751G=
19g.43551629C>GCA406203439XRCC1c.1141G>C (p.Val381Leu)
c.1048G>C (p.Val350Leu)
c.751G>C
 dbSNP gnomAD v4
19g.43551629C>TCA9488534XRCC1c.1141G>A (p.Val381Met)
c.1048G>A (p.Val350Met)
c.751G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.43551630G>ACA9488535XRCC1c.1140C>T (p.Ile380=)
c.1047C>T (p.Ile349=)
c.750C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551630G>CCA406203449XRCC1c.1140C>G (p.Ile380Met)
c.1047C>G (p.Ile349Met)
c.750C>G
 dbSNP
19g.43551630G=CA2337551285XRCC1c.1140C= (p.Ile380=)
c.1047C= (p.Ile349=)
c.750C=
19g.43551630G>TCA507741038XRCC1c.1140C>A (p.Ile380=)
c.1047C>A (p.Ile349=)
c.750C>A
 dbSNP
19g.43551631A>CCA406203451XRCC1c.1139T>G (p.Ile380Ser)
c.1046T>G (p.Ile349Ser)
c.749T>G
 dbSNP
19g.43551631A>GCA406203453XRCC1c.1139T>C (p.Ile380Thr)
c.1046T>C (p.Ile349Thr)
c.749T>C
19g.43551631A>TCA406203457XRCC1c.1139T>A (p.Ile380Asn)
c.1046T>A (p.Ile349Asn)
c.749T>A
 dbSNP
19g.43551632T>ACA406203459XRCC1c.1138A>T (p.Ile380Phe)
c.1045A>T (p.Ile349Phe)
c.748A>T
 dbSNP gnomAD v4
19g.43551632T>CCA308773418XRCC1c.1138A>G (p.Ile380Val)
c.1045A>G (p.Ile349Val)
c.748A>G
 dbSNP gnomAD v2 gnomAD v4
19g.43551632T>GCA406203461XRCC1c.1138A>C (p.Ile380Leu)
c.1045A>C (p.Ile349Leu)
c.748A>C
19g.43551632T=CA2337551286XRCC1c.1138A= (p.Ile380=)
c.1045A= (p.Ile349=)
c.748A=
19g.43551633G>ACA9488536XRCC1c.1137C>T (p.Arg379=)
c.1044C>T (p.Arg348=)
c.747C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551633G>CCA507741039XRCC1c.1137C>G (p.Arg379=)
c.1044C>G (p.Arg348=)
c.747C>G
 dbSNP
19g.43551633G=CA2337551287XRCC1c.1137C= (p.Arg379=)
c.1044C= (p.Arg348=)
c.747C=
19g.43551633G>TCA507741040XRCC1c.1137C>A (p.Arg379=)
c.1044C>A (p.Arg348=)
c.747C>A
 dbSNP
19g.43551634C>ACA406203464XRCC1c.1136G>T (p.Arg379Leu)
c.1043G>T (p.Arg348Leu)
c.746G>T
 gnomAD v4
19g.43551634C=CA2337551288XRCC1c.1136G= (p.Arg379=)
c.1043G= (p.Arg348=)
c.746G=
19g.43551634C>GCA406203467XRCC1c.1136G>C (p.Arg379Pro)
c.1043G>C (p.Arg348Pro)
c.746G>C
19g.43551634C>TCA9488537XRCC1c.1136G>A (p.Arg379His)
c.1043G>A (p.Arg348His)
c.746G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.43551635G>ACA9488538XRCC1c.1135C>T (p.Arg379Cys)
c.1042C>T (p.Arg348Cys)
c.745C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551635G>CCA406203470XRCC1c.1135C>G (p.Arg379Gly)
c.1042C>G (p.Arg348Gly)
c.745C>G
 dbSNP gnomAD v4
19g.43551635G=CA2337551289XRCC1c.1135C= (p.Arg379=)
c.1042C= (p.Arg348=)
c.745C=
19g.43551635G>TCA406203472XRCC1c.1135C>A (p.Arg379Ser)
c.1042C>A (p.Arg348Ser)
c.745C>A
 dbSNP gnomAD v4
19g.43551636G>ACA507741041XRCC1c.1134C>T (p.Gly378=)
c.1041C>T (p.Gly347=)
c.744C>T
 dbSNP
19g.43551636G>CCA507741042XRCC1c.1134C>G (p.Gly378=)
c.1041C>G (p.Gly347=)
c.744C>G
 dbSNP
19g.43551636G>TCA507741043XRCC1c.1134C>A (p.Gly378=)
c.1041C>A (p.Gly347=)
c.744C>A
 dbSNP
19g.43551637C>ACA406203474XRCC1c.1133G>T (p.Gly378Val)
c.1040G>T (p.Gly347Val)
c.743G>T
19g.43551637C>GCA406203476XRCC1c.1133G>C (p.Gly378Ala)
c.1040G>C (p.Gly347Ala)
c.743G>C
 dbSNP
19g.43551637C>TCA406203478XRCC1c.1133G>A (p.Gly378Asp)
c.1040G>A (p.Gly347Asp)
c.743G>A
 dbSNP
19g.43551638C>ACA406203480XRCC1c.1132G>T (p.Gly378Cys)
c.1039G>T (p.Gly347Cys)
c.742G>T
 dbSNP
19g.43551638C=CA2337551290XRCC1c.1132G= (p.Gly378=)
c.1039G= (p.Gly347=)
c.742G=
19g.43551638C>GCA406203482XRCC1c.1132G>C (p.Gly378Arg)
c.1039G>C (p.Gly347Arg)
c.742G>C
 dbSNP
19g.43551638C>TCA406203484XRCC1c.1132G>A (p.Gly378Ser)
c.1039G>A (p.Gly347Ser)
c.742G>A
 dbSNP gnomAD v2 gnomAD v4
19g.43551639T>ACA507741044XRCC1c.1131A>T (p.Gly377=)
c.1038A>T (p.Gly346=)
c.741A>T
19g.43551639T>CCA507741045XRCC1c.1131A>G (p.Gly377=)
c.1038A>G (p.Gly346=)
c.741A>G
19g.43551639T>GCA507741046XRCC1c.1131A>C (p.Gly377=)
c.1038A>C (p.Gly346=)
c.741A>C
19g.43551639_43551640delinsTCCA2337551291XRCC1c.1130_1131delinsGA (p.Gly377=)
c.1037_1038delinsGA (p.Gly346=)
c.740_741delinsGA
19g.43551640C>ACA406203503XRCC1c.1130G>T (p.Gly377Val)
c.1037G>T (p.Gly346Val)
c.740G>T
 dbSNP
19g.43551640C>GCA406203499XRCC1c.1130G>C (p.Gly377Ala)
c.1037G>C (p.Gly346Ala)
c.740G>C
 dbSNP
19g.43551640C>TCA406203501XRCC1c.1130G>A (p.Gly377Glu)
c.1037G>A (p.Gly346Glu)
c.740G>A
 dbSNP
19g.43551642delCA9488539XRCC1c.1130del (p.Gly377GlufsTer?)
c.1037del (p.Gly346GlufsTer?)
c.740del
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.43551641C>ACA406203509XRCC1c.1129G>T (p.Gly377Ter)
c.1036G>T (p.Gly346Ter)
c.739G>T
 dbSNP
19g.43551641C>GCA406203505XRCC1c.1129G>C (p.Gly377Arg)
c.1036G>C (p.Gly346Arg)
c.739G>C
 dbSNP
19g.43551641C>TCA406203507XRCC1c.1129G>A (p.Gly377Arg)
c.1036G>A (p.Gly346Arg)
c.739G>A
 dbSNP
19g.43551642C>ACA507741047XRCC1c.1128G>T (p.Leu376=)
c.1035G>T (p.Leu345=)
c.738G>T
 dbSNP
19g.43551642C=CA2337551292XRCC1c.1128G= (p.Leu376=)
c.1035G= (p.Leu345=)
c.738G=
19g.43551642C>GCA9488540XRCC1c.1128G>C (p.Leu376=)
c.1035G>C (p.Leu345=)
c.738G>C
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.43551642C>TCA507741048XRCC1c.1128G>A (p.Leu376=)
c.1035G>A (p.Leu345=)
c.738G>A
 dbSNP
19g.43551643A=CA2337551293XRCC1c.1127T= (p.Leu376=)
c.1034T= (p.Leu345=)
c.737T=
19g.43551643A>CCA406203512XRCC1c.1127T>G (p.Leu376Arg)
c.1034T>G (p.Leu345Arg)
c.737T>G
19g.43551643A>GCA406203514XRCC1c.1127T>C (p.Leu376Pro)
c.1034T>C (p.Leu345Pro)
c.737T>C
 dbSNP
19g.43551643A>TCA406203516XRCC1c.1127T>A (p.Leu376Gln)
c.1034T>A (p.Leu345Gln)
c.737T>A
 dbSNP
19g.43551644G>ACA507741049XRCC1c.1126C>T (p.Leu376=)
c.1033C>T (p.Leu345=)
c.736C>T
 dbSNP gnomAD v3 gnomAD v4
19g.43551644G>CCA406203518XRCC1c.1126C>G (p.Leu376Val)
c.1033C>G (p.Leu345Val)
c.736C>G
19g.43551644G=CA2337551294XRCC1c.1126C= (p.Leu376=)
c.1033C= (p.Leu345=)
c.736C=
19g.43551644G>TCA406203519XRCC1c.1126C>A (p.Leu376Met)
c.1033C>A (p.Leu345Met)
c.736C>A
19g.43551645G>ACA507741050XRCC1c.1125C>T (p.Gly375=)
c.1032C>T (p.Gly344=)
c.735C>T
 dbSNP gnomAD v4
19g.43551645G>CCA507741051XRCC1c.1125C>G (p.Gly375=)
c.1032C>G (p.Gly344=)
c.735C>G
 dbSNP
19g.43551645G>TCA507741052XRCC1c.1125C>A (p.Gly375=)
c.1032C>A (p.Gly344=)
c.735C>A
19g.43551646C>ACA406203522XRCC1c.1124G>T (p.Gly375Val)
c.1031G>T (p.Gly344Val)
c.734G>T
 dbSNP
19g.43551646C>GCA406203524XRCC1c.1124G>C (p.Gly375Ala)
c.1031G>C (p.Gly344Ala)
c.734G>C
 dbSNP
19g.43551646C>TCA406203526XRCC1c.1124G>A (p.Gly375Asp)
c.1031G>A (p.Gly344Asp)
c.734G>A
 dbSNP
19g.43551647C>ACA406203532XRCC1c.1123G>T (p.Gly375Cys)
c.1030G>T (p.Gly344Cys)
c.733G>T
 dbSNP
19g.43551647C>GCA406203530XRCC1c.1123G>C (p.Gly375Arg)
c.1030G>C (p.Gly344Arg)
c.733G>C
 dbSNP
19g.43551647C>TCA406203528XRCC1c.1123G>A (p.Gly375Ser)
c.1030G>A (p.Gly344Ser)
c.733G>A
19g.43551648T>ACA507741053XRCC1c.1122A>T (p.Leu374=)
c.1029A>T (p.Leu343=)
c.732A>T
 dbSNP
19g.43551648T>CCA507741054XRCC1c.1122A>G (p.Leu374=)
c.1029A>G (p.Leu343=)
c.732A>G
 dbSNP gnomAD v4
19g.43551648T>GCA507741055XRCC1c.1122A>C (p.Leu374=)
c.1029A>C (p.Leu343=)
c.732A>C
19g.43551649A>CCA406203533XRCC1c.1121T>G (p.Leu374Arg)
c.1028T>G (p.Leu343Arg)
c.731T>G
 dbSNP
19g.43551649A>GCA406203535XRCC1c.1121T>C (p.Leu374Pro)
c.1028T>C (p.Leu343Pro)
c.731T>C
 dbSNP COSMIC
19g.43551649A>TCA406203537XRCC1c.1121T>A (p.Leu374Gln)
c.1028T>A (p.Leu343Gln)
c.731T>A
 dbSNP
19g.43551650G>ACA507741056XRCC1c.1120C>T (p.Leu374=)
c.1027C>T (p.Leu343=)
c.730C>T
 dbSNP
19g.43551650G>CCA406203539XRCC1c.1120C>G (p.Leu374Val)
c.1027C>G (p.Leu343Val)
c.730C>G
 dbSNP gnomAD v3 gnomAD v4
19g.43551650G=CA2337551295XRCC1c.1120C= (p.Leu374=)
c.1027C= (p.Leu343=)
c.730C=
19g.43551650G>TCA406203541XRCC1c.1120C>A (p.Leu374Ile)
c.1027C>A (p.Leu343Ile)
c.730C>A
 dbSNP
19g.43551651G>ACA507741057XRCC1c.1119C>T (p.Val373=)
c.1026C>T (p.Val342=)
c.729C>T
 dbSNP
19g.43551651G>CCA507741058XRCC1c.1119C>G (p.Val373=)
c.1026C>G (p.Val342=)
c.729C>G
 dbSNP
19g.43551651G>TCA507741059XRCC1c.1119C>A (p.Val373=)
c.1026C>A (p.Val342=)
c.729C>A
19g.43551652A>CCA406203543XRCC1c.1118T>G (p.Val373Gly)
c.1025T>G (p.Val342Gly)
c.728T>G
 dbSNP
19g.43551652A>GCA406203545XRCC1c.1118T>C (p.Val373Ala)
c.1025T>C (p.Val342Ala)
c.728T>C
 dbSNP
19g.43551652A>TCA406203547XRCC1c.1118T>A (p.Val373Asp)
c.1025T>A (p.Val342Asp)
c.728T>A
 dbSNP
19g.43551653C>ACA406203549XRCC1c.1117G>T (p.Val373Phe)
c.1024G>T (p.Val342Phe)
c.727G>T
 dbSNP
19g.43551653C>GCA406203551XRCC1c.1117G>C (p.Val373Leu)
c.1024G>C (p.Val342Leu)
c.727G>C
 dbSNP
19g.43551653C>TCA406203553XRCC1c.1117G>A (p.Val373Ile)
c.1024G>A (p.Val342Ile)
c.727G>A
 dbSNP gnomAD v4
19g.43551654C>ACA406203555XRCC1c.1116G>T (p.Gln372His)
c.1023G>T (p.Gln341His)
c.726G>T
19g.43551654C>GCA406203557XRCC1c.1116G>C (p.Gln372His)
c.1023G>C (p.Gln341His)
c.726G>C
 dbSNP
19g.43551654C>TCA507741060XRCC1c.1116G>A (p.Gln372=)
c.1023G>A (p.Gln341=)
c.726G>A
 gnomAD v4
19g.43551655T>ACA406203559XRCC1c.1115A>T (p.Gln372Leu)
c.1022A>T (p.Gln341Leu)
c.725A>T
19g.43551655T>CCA406203563XRCC1c.1115A>G (p.Gln372Arg)
c.1022A>G (p.Gln341Arg)
c.725A>G
19g.43551655T>GCA406203561XRCC1c.1115A>C (p.Gln372Pro)
c.1022A>C (p.Gln341Pro)
c.725A>C
19g.43551656G>ACA9488541XRCC1c.1114C>T (p.Gln372Ter)
c.1021C>T (p.Gln341Ter)
c.724C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551656G>CCA406203568XRCC1c.1114C>G (p.Gln372Glu)
c.1021C>G (p.Gln341Glu)
c.724C>G
 dbSNP
19g.43551656G=CA2337551296XRCC1c.1114C= (p.Gln372=)
c.1021C= (p.Gln341=)
c.724C=
19g.43551656G>TCA406203566XRCC1c.1114C>A (p.Gln372Lys)
c.1021C>A (p.Gln341Lys)
c.724C>A
19g.43551657G>ACA507741061XRCC1c.1113C>T (p.Ser371=)
c.1020C>T (p.Ser340=)
c.723C>T
 dbSNP
19g.43551657G>CCA406203571XRCC1c.1113C>G (p.Ser371Arg)
c.1020C>G (p.Ser340Arg)
c.723C>G
 dbSNP
19g.43551657G>TCA406203573XRCC1c.1113C>A (p.Ser371Arg)
c.1020C>A (p.Ser340Arg)
c.723C>A
 dbSNP
19g.43551658C>ACA406203574XRCC1c.1112G>T (p.Ser371Ile)
c.1019G>T (p.Ser340Ile)
c.722G>T
19g.43551658C>GCA406203576XRCC1c.1112G>C (p.Ser371Thr)
c.1019G>C (p.Ser340Thr)
c.722G>C
 dbSNP gnomAD v4
19g.43551658C>TCA406203578XRCC1c.1112G>A (p.Ser371Asn)
c.1019G>A (p.Ser340Asn)
c.722G>A
 dbSNP
19g.43551659T>ACA406203581XRCC1c.1111A>T (p.Ser371Cys)
c.1018A>T (p.Ser340Cys)
c.721A>T
 dbSNP
19g.43551659T>CCA406203583XRCC1c.1111A>G (p.Ser371Gly)
c.1018A>G (p.Ser340Gly)
c.721A>G
19g.43551659T>GCA406203585XRCC1c.1111A>C (p.Ser371Arg)
c.1018A>C (p.Ser340Arg)
c.721A>C
19g.43551660G>ACA507741062XRCC1c.1110C>T (p.Tyr370=)
c.1017C>T (p.Tyr339=)
c.720C>T
 dbSNP
19g.43551660G>CCA406203587XRCC1c.1110C>G (p.Tyr370Ter)
c.1017C>G (p.Tyr339Ter)
c.720C>G
 dbSNP
19g.43551660G>TCA406203589XRCC1c.1110C>A (p.Tyr370Ter)
c.1017C>A (p.Tyr339Ter)
c.720C>A
19g.43551661T>ACA406203591XRCC1c.1109A>T (p.Tyr370Phe)
c.1016A>T (p.Tyr339Phe)
c.719A>T
 dbSNP
19g.43551661T>CCA9488542XRCC1c.1109A>G (p.Tyr370Cys)
c.1016A>G (p.Tyr339Cys)
c.719A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.43551661T>GCA406203592XRCC1c.1109A>C (p.Tyr370Ser)
c.1016A>C (p.Tyr339Ser)
c.719A>C
 dbSNP
19g.43551661T=CA2337551297XRCC1c.1109A= (p.Tyr370=)
c.1016A= (p.Tyr339=)
c.719A=
19g.43551662A=CA2337551298XRCC1c.1108T= (p.Tyr370=)
c.1015T= (p.Tyr339=)
c.718T=
19g.43551662A>CCA406203598XRCC1c.1108T>G (p.Tyr370Asp)
c.1015T>G (p.Tyr339Asp)
c.718T>G
 dbSNP
19g.43551662A>GCA406203596XRCC1c.1108T>C (p.Tyr370His)
c.1015T>C (p.Tyr339His)
c.718T>C
 dbSNP
19g.43551662A>TCA406203595XRCC1c.1108T>A (p.Tyr370Asn)
c.1015T>A (p.Tyr339Asn)
c.718T>A
 dbSNP gnomAD v2 gnomAD v4
19g.43551663C>ACA406203600XRCC1c.1107G>T (p.Lys369Asn)
c.1014G>T (p.Lys338Asn)
c.717G>T
 dbSNP
19g.43551663C=CA2337551299XRCC1c.1107G= (p.Lys369=)
c.1014G= (p.Lys338=)
c.717G=
19g.43551663C>GCA406203602XRCC1c.1107G>C (p.Lys369Asn)
c.1014G>C (p.Lys338Asn)
c.717G>C
 dbSNP
19g.43551663C>TCA507741063XRCC1c.1107G>A (p.Lys369=)
c.1014G>A (p.Lys338=)
c.717G>A
 dbSNP gnomAD v4
19g.43551664T>ACA406203604XRCC1c.1106A>T (p.Lys369Met)
c.1013A>T (p.Lys338Met)
c.716A>T
 dbSNP
19g.43551664T>CCA406203606XRCC1c.1106A>G (p.Lys369Arg)
c.1013A>G (p.Lys338Arg)
c.716A>G
 gnomAD v4
19g.43551664T>GCA406203608XRCC1c.1106A>C (p.Lys369Thr)
c.1013A>C (p.Lys338Thr)
c.716A>C
19g.43551665T>ACA406203610XRCC1c.1105A>T (p.Lys369Ter)
c.1012A>T (p.Lys338Ter)
c.715A>T
19g.43551665T>CCA406203612XRCC1c.1105A>G (p.Lys369Glu)
c.1012A>G (p.Lys338Glu)
c.715A>G
19g.43551665T>GCA406203613XRCC1c.1105A>C (p.Lys369Gln)
c.1012A>C (p.Lys338Gln)
c.715A>C
19g.43551666G>ACA9488543XRCC1c.1104C>T (p.Pro368=)
c.1011C>T (p.Pro337=)
c.714C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.43551666G>CCA507741064XRCC1c.1104C>G (p.Pro368=)
c.1011C>G (p.Pro337=)
c.714C>G
19g.43551666G=CA2337551300XRCC1c.1104C= (p.Pro368=)
c.1011C= (p.Pro337=)
c.714C=
19g.43551666G>TCA507741065XRCC1c.1104C>A (p.Pro368=)
c.1011C>A (p.Pro337=)
c.714C>A
19g.43551667G>ACA406203617XRCC1c.1103C>T (p.Pro368Leu)
c.1010C>T (p.Pro337Leu)
c.713C>T
 dbSNP COSMIC
19g.43551667G>CCA406203619XRCC1c.1103C>G (p.Pro368Arg)
c.1010C>G (p.Pro337Arg)
c.713C>G
 dbSNP
19g.43551667G>TCA406203621XRCC1c.1103C>A (p.Pro368His)
c.1010C>A (p.Pro337His)
c.713C>A
 dbSNP
19g.43551668G>ACA406203627XRCC1c.1102C>T (p.Pro368Ser)
c.1009C>T (p.Pro337Ser)
c.712C>T
 dbSNP gnomAD v4
19g.43551668G>CCA406203624XRCC1c.1102C>G (p.Pro368Ala)
c.1009C>G (p.Pro337Ala)
c.712C>G
 dbSNP
19g.43551668G>TCA406203623XRCC1c.1102C>A (p.Pro368Thr)
c.1009C>A (p.Pro337Thr)
c.712C>A
 dbSNP
19g.43551669G>ACA507741066XRCC1c.1101C>T (p.Thr367=)
c.1008C>T (p.Thr336=)
c.711C>T
 dbSNP
19g.43551669G>CCA507741067XRCC1c.1101C>G (p.Thr367=)
c.1008C>G (p.Thr336=)
c.711C>G
 dbSNP
19g.43551669G>TCA507741068XRCC1c.1101C>A (p.Thr367=)
c.1008C>A (p.Thr336=)
c.711C>A
 dbSNP
19g.43551670G>ACA406203629XRCC1c.1100C>T (p.Thr367Ile)
c.1007C>T (p.Thr336Ile)
c.710C>T
 dbSNP
19g.43551670G>CCA406203631XRCC1c.1100C>G (p.Thr367Ser)
c.1007C>G (p.Thr336Ser)
c.710C>G
 dbSNP
19g.43551670G>TCA406203632XRCC1c.1100C>A (p.Thr367Asn)
c.1007C>A (p.Thr336Asn)
c.710C>A
19g.43551671T>ACA406203633XRCC1c.1099A>T (p.Thr367Ser)
c.1006A>T (p.Thr336Ser)
c.709A>T
 dbSNP
19g.43551671T>CCA406203634XRCC1c.1099A>G (p.Thr367Ala)
c.1006A>G (p.Thr336Ala)
c.709A>G
19g.43551671T>GCA406203636XRCC1c.1099A>C (p.Thr367Pro)
c.1006A>C (p.Thr336Pro)
c.709A>C
 dbSNP
19g.43551671T=CA2337550678XRCC1c.1099A= (p.Thr367=)
c.1006A= (p.Thr336=)
c.709A=
19g.43551672G>ACA507741069XRCC1c.1098C>T (p.Asn366=)
c.1005C>T (p.Asn335=)
c.708C>T
 dbSNP gnomAD v4
19g.43551672G>CCA406203640XRCC1c.1098C>G (p.Asn366Lys)
c.1005C>G (p.Asn335Lys)
c.708C>G
 dbSNP
19g.43551672G>TCA406203638XRCC1c.1098C>A (p.Asn366Lys)
c.1005C>A (p.Asn335Lys)
c.708C>A
 dbSNP
19g.43551673T>ACA406203642XRCC1c.1097A>T (p.Asn366Ile)
c.1004A>T (p.Asn335Ile)
c.707A>T
 dbSNP
19g.43551673T>CCA308773454XRCC1c.1097A>G (p.Asn366Ser)
c.1004A>G (p.Asn335Ser)
c.707A>G
 dbSNP gnomAD v3 gnomAD v4
19g.43551673T>GCA406203645XRCC1c.1097A>C (p.Asn366Thr)
c.1004A>C (p.Asn335Thr)
c.707A>C
 dbSNP
19g.43551673T=CA2337551301XRCC1c.1097A= (p.Asn366=)
c.1004A= (p.Asn335=)
c.707A=
19g.43551674T>ACA406203647XRCC1c.1096A>T (p.Asn366Tyr)
c.1003A>T (p.Asn335Tyr)
c.706A>T
 dbSNP
19g.43551674T>CCA406203649XRCC1c.1096A>G (p.Asn366Asp)
c.1003A>G (p.Asn335Asp)
c.706A>G
19g.43551674T>GCA406203651XRCC1c.1096A>C (p.Asn366His)
c.1003A>C (p.Asn335His)
c.706A>C
 dbSNP
19g.43551675G>ACA507741070XRCC1c.1095C>T (p.Ala365=)
c.1002C>T (p.Ala334=)
c.705C>T
 dbSNP gnomAD v4
19g.43551675G>CCA507741071XRCC1c.1095C>G (p.Ala365=)
c.1002C>G (p.Ala334=)
c.705C>G
 dbSNP
19g.43551675G>TCA507741072XRCC1c.1095C>A (p.Ala365=)
c.1002C>A (p.Ala334=)
c.705C>A
19g.43551676G>ACA9488544XRCC1c.1094C>T (p.Ala365Val)
c.1001C>T (p.Ala334Val)
c.704C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551676G>CCA406203656XRCC1c.1094C>G (p.Ala365Gly)
c.1001C>G (p.Ala334Gly)
c.704C>G
 dbSNP
19g.43551676G=CA2337551302XRCC1c.1094C= (p.Ala365=)
c.1001C= (p.Ala334=)
c.704C=
19g.43551676G>TCA406203654XRCC1c.1094C>A (p.Ala365Asp)
c.1001C>A (p.Ala334Asp)
c.704C>A
19g.43551677C>ACA406203658XRCC1c.1093G>T (p.Ala365Ser)
c.1000G>T (p.Ala334Ser)
c.703G>T
19g.43551677C>GCA406203660XRCC1c.1093G>C (p.Ala365Pro)
c.1000G>C (p.Ala334Pro)
c.703G>C
19g.43551677C>TCA406203661XRCC1c.1093G>A (p.Ala365Thr)
c.1000G>A (p.Ala334Thr)
c.703G>A
 dbSNP COSMIC
19g.43551678A>CCA406203664XRCC1c.1092T>G (p.Phe364Leu)
c.999T>G (p.Phe333Leu)
c.702T>G
19g.43551678A>GCA507741073XRCC1c.1092T>C (p.Phe364=)
c.999T>C (p.Phe333=)
c.702T>C
19g.43551678A>TCA406203665XRCC1c.1092T>A (p.Phe364Leu)
c.999T>A (p.Phe333Leu)
c.702T>A
19g.43551679A>CCA406203666XRCC1c.1091T>G (p.Phe364Cys)
c.998T>G (p.Phe333Cys)
c.701T>G
 dbSNP
19g.43551679A>GCA406203668XRCC1c.1091T>C (p.Phe364Ser)
c.998T>C (p.Phe333Ser)
c.701T>C
 dbSNP
19g.43551679A>TCA406203670XRCC1c.1091T>A (p.Phe364Tyr)
c.998T>A (p.Phe333Tyr)
c.701T>A
19g.43551680A>CCA406203671XRCC1c.1090T>G (p.Phe364Val)
c.997T>G (p.Phe333Val)
c.700T>G
19g.43551680A>GCA406203674XRCC1c.1090T>C (p.Phe364Leu)
c.997T>C (p.Phe333Leu)
c.700T>C
 dbSNP
19g.43551680A>TCA406203676XRCC1c.1090T>A (p.Phe364Ile)
c.997T>A (p.Phe333Ile)
c.700T>A
 dbSNP
19g.43551681G>ACA9488545XRCC1c.1089C>T (p.Ala363=)
c.996C>T (p.Ala332=)
c.699C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551681G>CCA507741074XRCC1c.1089C>G (p.Ala363=)
c.996C>G (p.Ala332=)
c.699C>G
 dbSNP gnomAD v4
19g.43551681G=CA2337551303XRCC1c.1089C= (p.Ala363=)
c.996C= (p.Ala332=)
c.699C=
19g.43551681G>TCA507741075XRCC1c.1089C>A (p.Ala363=)
c.996C>A (p.Ala332=)
c.699C>A
 dbSNP
19g.43551682G>ACA406203682XRCC1c.1088C>T (p.Ala363Val)
c.995C>T (p.Ala332Val)
c.698C>T
 dbSNP
19g.43551682G>CCA406203680XRCC1c.1088C>G (p.Ala363Gly)
c.995C>G (p.Ala332Gly)
c.698C>G
 dbSNP
19g.43551682G>TCA406203684XRCC1c.1088C>A (p.Ala363Asp)
c.995C>A (p.Ala332Asp)
c.698C>A
19g.43551683C>ACA406203686XRCC1c.1087G>T (p.Ala363Ser)
c.994G>T (p.Ala332Ser)
c.697G>T
 dbSNP
19g.43551683C=CA2337551304XRCC1c.1087G= (p.Ala363=)
c.994G= (p.Ala332=)
c.697G=
19g.43551683C>GCA406203688XRCC1c.1087G>C (p.Ala363Pro)
c.994G>C (p.Ala332Pro)
c.697G>C
 dbSNP
19g.43551683C>TCA9488546XRCC1c.1087G>A (p.Ala363Thr)
c.994G>A (p.Ala332Thr)
c.697G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.43551684A>CCA406203691XRCC1c.1086T>G (p.Cys362Trp)
c.993T>G (p.Cys331Trp)
c.696T>G
 dbSNP gnomAD v4
19g.43551684A>GCA507741076XRCC1c.1086T>C (p.Cys362=)
c.993T>C (p.Cys331=)
c.696T>C
 dbSNP
19g.43551684A>TCA406203692XRCC1c.1086T>A (p.Cys362Ter)
c.993T>A (p.Cys331Ter)
c.696T>A
 dbSNP
19g.43551685C>ACA406203695XRCC1c.1085G>T (p.Cys362Phe)
c.992G>T (p.Cys331Phe)
c.695G>T
 dbSNP
19g.43551685C=CA2337551305XRCC1c.1085G= (p.Cys362=)
c.992G= (p.Cys331=)
c.695G=
19g.43551685C>GCA406203697XRCC1c.1085G>C (p.Cys362Ser)
c.992G>C (p.Cys331Ser)
c.695G>C
 dbSNP gnomAD v3 gnomAD v4
19g.43551685C>TCA406203698XRCC1c.1085G>A (p.Cys362Tyr)
c.992G>A (p.Cys331Tyr)
c.695G>A
 dbSNP gnomAD v2 gnomAD v4
19g.43551686A>CCA406203700XRCC1c.1084T>G (p.Cys362Gly)
c.991T>G (p.Cys331Gly)
c.694T>G
19g.43551686A>GCA406203702XRCC1c.1084T>C (p.Cys362Arg)
c.991T>C (p.Cys331Arg)
c.694T>C
 dbSNP
19g.43551686A>TCA406203704XRCC1c.1084T>A (p.Cys362Ser)
c.991T>A (p.Cys331Ser)
c.694T>A
 dbSNP
19g.43551687G>ACA507741077XRCC1c.1083C>T (p.Ile361=)
c.990C>T (p.Ile330=)
c.693C>T
 dbSNP
19g.43551687G>CCA406203706XRCC1c.1083C>G (p.Ile361Met)
c.990C>G (p.Ile330Met)
c.693C>G
 dbSNP
19g.43551687G>TCA507741078XRCC1c.1083C>A (p.Ile361=)
c.990C>A (p.Ile330=)
c.693C>A
19g.43551688C>ACA406203711XRCC1c.1083-1G>T (n.1083-1G>T)
c.990-1G>T (n.990-1G>T)
c.693-1G>T
 dbSNP
19g.43551688C>GCA406203710XRCC1c.1083-1G>C (n.1083-1G>C)
c.990-1G>C (n.990-1G>C)
c.693-1G>C
 dbSNP gnomAD v4
19g.43551688C>TCA406203709XRCC1c.1083-1G>A (n.1083-1G>A)
c.990-1G>A (n.990-1G>A)
c.693-1G>A
 dbSNP gnomAD v4
19g.43551689T>ACA406203714XRCC1c.1083-2A>T (n.1083-2A>T)
c.990-2A>T (n.990-2A>T)
c.693-2A>T
19g.43551689T>CCA406203715XRCC1c.1083-2A>G (n.1083-2A>G)
c.990-2A>G (n.990-2A>G)
c.693-2A>G
19g.43551689T>GCA406203717XRCC1c.1083-2A>C (n.1083-2A>C)
c.990-2A>C (n.990-2A>C)
c.693-2A>C
19g.43551690G>ACA2736077785XRCC1c.1083-3C>T (n.1083-3C>T)
c.990-3C>T (n.990-3C>T)
c.693-3C>T
 dbSNP
19g.43551690G>CCA2736077582XRCC1c.1083-3C>G (n.1083-3C>G)
c.990-3C>G (n.990-3C>G)
c.693-3C>G
 dbSNP
19g.43551691G>ACA2585526201XRCC1c.1083-4C>T (n.1083-4C>T)
c.990-4C>T (n.990-4C>T)
c.693-4C>T
 dbSNP gnomAD v4
19g.43551691G>CCA9488547XRCC1c.1083-4C>G (n.1083-4C>G)
c.990-4C>G (n.990-4C>G)
c.693-4C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551691G=CA2337551306XRCC1c.1083-4C= (n.1083-4C=)
c.990-4C= (n.990-4C=)
c.693-4C=
19g.43551691G>TCA2735879270XRCC1c.1083-4C>A (n.1083-4C>A)
c.990-4C>A (n.990-4C>A)
c.693-4C>A
 dbSNP
19g.43551692T>ACA633476300XRCC1c.1083-5A>T (n.1083-5A>T)
c.990-5A>T (n.990-5A>T)
c.693-5A>T
 dbSNP gnomAD v2 gnomAD v4
19g.43551692T>CCA2585526202XRCC1c.1083-5A>G (n.1083-5A>G)
c.990-5A>G (n.990-5A>G)
c.693-5A>G
 gnomAD v4
19g.43551692T>GCA2337551307XRCC1c.1083-5A>C (n.1083-5A>C)
c.990-5A>C (n.990-5A>C)
c.693-5A>C
 dbSNP
19g.43551692T=CA2337551308XRCC1c.1083-5A= (n.1083-5A=)
c.990-5A= (n.990-5A=)
c.693-5A=
19g.43551693G>ACA2735882392XRCC1c.1083-6C>T (n.1083-6C>T)
c.990-6C>T (n.990-6C>T)
c.693-6C>T
 dbSNP
19g.43551693G>CCA2337551310XRCC1c.1083-6C>G (n.1083-6C>G)
c.990-6C>G (n.990-6C>G)
c.693-6C>G
 dbSNP
19g.43551693G=CA2337551309XRCC1c.1083-6C= (n.1083-6C=)
c.990-6C= (n.990-6C=)
c.693-6C=
19g.43551693G>TCA9488549XRCC1c.1083-6C>A (n.1083-6C>A)
c.990-6C>A (n.990-6C>A)
c.693-6C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.43551698dupCA9488548XRCC1c.1083-6dup (n.1083-6dup)
c.990-6dup (n.990-6dup)
c.693-6dup
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551698delCA2585526203XRCC1c.1083-6del (n.1083-6del)
c.990-6del (n.990-6del)
c.693-6del
 gnomAD v4
19g.43551694G>ACA2585526204XRCC1c.1083-7C>T (n.1083-7C>T)
c.990-7C>T (n.990-7C>T)
c.693-7C>T
 dbSNP gnomAD v4
19g.43551694G>CCA882544321XRCC1c.1083-7C>G (n.1083-7C>G)
c.990-7C>G (n.990-7C>G)
c.693-7C>G
 dbSNP
19g.43551694G=CA2337551311XRCC1c.1083-7C= (n.1083-7C=)
c.990-7C= (n.990-7C=)
c.693-7C=
19g.43551694G>TCA2585526205XRCC1c.1083-7C>A (n.1083-7C>A)
c.990-7C>A (n.990-7C>A)
c.693-7C>A
 dbSNP gnomAD v4
19g.43551695G>ACA2736077869XRCC1c.1083-8C>T (n.1083-8C>T)
c.990-8C>T (n.990-8C>T)
c.693-8C>T
 dbSNP
19g.43551696G>ACA9488550XRCC1c.1083-9C>T (n.1083-9C>T)
c.990-9C>T (n.990-9C>T)
c.693-9C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551696G>CCA2337551313XRCC1c.1083-9C>G (n.1083-9C>G)
c.990-9C>G (n.990-9C>G)
c.693-9C>G
 dbSNP gnomAD v4
19g.43551696G=CA2337551312XRCC1c.1083-9C= (n.1083-9C=)
c.990-9C= (n.990-9C=)
c.693-9C=
19g.43551697G>ACA9488551XRCC1c.1083-10C>T (n.1083-10C>T)
c.990-10C>T (n.990-10C>T)
c.693-10C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.43551697G=CA2337551314XRCC1c.1083-10C= (n.1083-10C=)
c.990-10C= (n.990-10C=)
c.693-10C=
19g.43551697G>TCA2735883850XRCC1c.1083-10C>A (n.1083-10C>A)
c.990-10C>A (n.990-10C>A)
c.693-10C>A
 dbSNP
19g.43551698G>ACA633476302XRCC1c.1083-11C>T (n.1083-11C>T)
c.990-11C>T (n.990-11C>T)
c.693-11C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.43551698G>CCA2585526206XRCC1c.1083-11C>G (n.1083-11C>G)
c.990-11C>G (n.990-11C>G)
c.693-11C>G
 gnomAD v4
19g.43551698G=CA2337551315XRCC1c.1083-11C= (n.1083-11C=)
c.990-11C= (n.990-11C=)
c.693-11C=
19g.43551698G>TCA9488552XRCC1c.1083-11C>A (n.1083-11C>A)
c.990-11C>A (n.990-11C>A)
c.693-11C>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.43551699C>ACA308773505XRCC1c.1083-12G>T (n.1083-12G>T)
c.990-12G>T (n.990-12G>T)
c.693-12G>T
 dbSNP gnomAD v3 gnomAD v4
19g.43551699C=CA2337551316XRCC1c.1083-12G= (n.1083-12G=)
c.990-12G= (n.990-12G=)
c.693-12G=
19g.43551699C>GCA2735890770XRCC1c.1083-12G>C (n.1083-12G>C)
c.990-12G>C (n.990-12G>C)
c.693-12G>C
 dbSNP
19g.43551699C>TCA2585526207XRCC1c.1083-12G>A (n.1083-12G>A)
c.990-12G>A (n.990-12G>A)
c.693-12G>A
 dbSNP gnomAD v4
19g.43551700A>TCA2736077883XRCC1c.1083-13T>A (n.1083-13T>A)
c.990-13T>A (n.990-13T>A)
c.693-13T>A
 dbSNP
19g.43551701G>ACA2736077885XRCC1c.1083-14C>T (n.1083-14C>T)
c.990-14C>T (n.990-14C>T)
c.693-14C>T
 dbSNP
19g.43551701G>CCA2576914482XRCC1c.1083-14C>G (n.1083-14C>G)
c.990-14C>G (n.990-14C>G)
c.693-14C>G
 gnomAD v4
19g.43551702A>CCA2585526208XRCC1c.1083-15T>G (n.1083-15T>G)
c.990-15T>G (n.990-15T>G)
c.693-15T>G
 dbSNP gnomAD v4
19g.43551702A>GCA2736077909XRCC1c.1083-15T>C (n.1083-15T>C)
c.990-15T>C (n.990-15T>C)
c.693-15T>C
 dbSNP
19g.43551703A>GCA657409410XRCC1c.1083-16T>C (n.1083-16T>C)
c.990-16T>C (n.990-16T>C)
c.693-16T>C
 COSMIC
19g.43551704G>ACA882544334XRCC1c.1083-17C>T (n.1083-17C>T)
c.990-17C>T (n.990-17C>T)
c.693-17C>T
 dbSNP gnomAD v3 gnomAD v4
19g.43551704G=CA2337551317XRCC1c.1083-17C= (n.1083-17C=)
c.990-17C= (n.990-17C=)
c.693-17C=
19g.43551705T>ACA2735908220XRCC1c.1083-18A>T (n.1083-18A>T)
c.990-18A>T (n.990-18A>T)
c.693-18A>T
 dbSNP
19g.43551705T>CCA633476303XRCC1c.1083-18A>G (n.1083-18A>G)
c.990-18A>G (n.990-18A>G)
c.693-18A>G
 dbSNP gnomAD v2 gnomAD v4
19g.43551705T>GCA2735908219XRCC1c.1083-18A>C (n.1083-18A>C)
c.990-18A>C (n.990-18A>C)
c.693-18A>C
 dbSNP
19g.43551705T=CA2337551318XRCC1c.1083-18A= (n.1083-18A=)
c.990-18A= (n.990-18A=)
c.693-18A=

Number of alleles fetched