ClinVar Miner

List of variants in gene XRCC2 reported as uncertain significance by GeneDx

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.613T>G (p.Ser205Ala) rs56103026 0.00017
NM_005431.2(XRCC2):c.662T>C (p.Ile221Thr) rs3218537 0.00016
NM_005431.2(XRCC2):c.643C>T (p.Arg215Ter) rs143153871 0.00006
NM_005431.2(XRCC2):c.115G>A (p.Val39Met) rs730882040 0.00005
NM_005431.2(XRCC2):c.476G>A (p.Arg159His) rs367696886 0.00005
NM_005431.2(XRCC2):c.580A>G (p.Thr194Ala) rs180805457 0.00005
NM_005431.2(XRCC2):c.271C>T (p.Arg91Trp) rs730882043 0.00004
NM_005431.2(XRCC2):c.450C>G (p.Ser150Arg) rs371453207 0.00004
NM_005431.2(XRCC2):c.475C>T (p.Arg159Cys) rs587780128 0.00004
NM_005431.2(XRCC2):c.562C>T (p.Arg188Cys) rs139219364 0.00004
NM_005431.2(XRCC2):c.773G>A (p.Arg258His) rs149186933 0.00004
NM_005431.2(XRCC2):c.641G>A (p.Arg214Gln) rs368445278 0.00003
NM_005431.2(XRCC2):c.262G>T (p.Asp88Tyr) rs958403796 0.00002
NM_005431.2(XRCC2):c.482A>G (p.Asn161Ser) rs1064794505 0.00002
NM_005431.2(XRCC2):c.50G>A (p.Arg17Gln) rs759291002 0.00002
NM_005431.2(XRCC2):c.596T>C (p.Met199Thr) rs149099078 0.00002
NM_005431.2(XRCC2):c.644G>A (p.Arg215Gln) rs762828701 0.00002
NM_005431.2(XRCC2):c.667T>C (p.Tyr223His) rs587780130 0.00002
NM_005431.2(XRCC2):c.770C>T (p.Ser257Leu) rs730882047 0.00002
NM_005431.2(XRCC2):c.119A>G (p.His40Arg) rs777753452 0.00001
NM_005431.2(XRCC2):c.140A>G (p.His47Arg) rs587780126 0.00001
NM_005431.2(XRCC2):c.181C>A (p.Leu61Ile) rs569810249 0.00001
NM_005431.2(XRCC2):c.383T>C (p.Leu128Pro) rs143220835 0.00001
NM_005431.2(XRCC2):c.478G>A (p.Val160Ile) rs144079294 0.00001
NM_005431.2(XRCC2):c.640C>T (p.Arg214Ter) rs1200646566 0.00001
NM_005431.2(XRCC2):c.714G>C (p.Arg238Ser) rs534746330 0.00001
NM_005431.2(XRCC2):c.734A>G (p.Asp245Gly) rs749779141 0.00001
NM_005431.2(XRCC2):c.7A>G (p.Ser3Gly) rs762701579 0.00001
NM_005431.2(XRCC2):c.803del (p.His268fs) rs776336749 0.00001
NM_005431.2(XRCC2):c.91C>G (p.Leu31Val) rs748198457 0.00001
NM_005431.2(XRCC2):c.106G>A (p.Asp36Asn) rs749538198
NM_005431.2(XRCC2):c.16_17insGAA (p.His6delinsArgAsn) rs1064794354
NM_005431.2(XRCC2):c.182T>C (p.Leu61Pro) rs730882041
NM_005431.2(XRCC2):c.199C>T (p.Leu67Phe) rs757259215
NM_005431.2(XRCC2):c.232G>A (p.Val78Ile) rs879254167
NM_005431.2(XRCC2):c.254A>C (p.Tyr85Ser) rs730882042
NM_005431.2(XRCC2):c.268C>G (p.Leu90Val) rs587780127
NM_005431.2(XRCC2):c.350dup (p.Leu117fs) rs764640893
NM_005431.2(XRCC2):c.353T>G (p.Val118Gly) rs185815454
NM_005431.2(XRCC2):c.367A>G (p.Ser123Gly) rs1064793296
NM_005431.2(XRCC2):c.391T>C (p.Tyr131His) rs1064793473
NM_005431.2(XRCC2):c.40C>T (p.Leu14Phe) rs1029144797
NM_005431.2(XRCC2):c.433C>G (p.Leu145Val) rs1060502669
NM_005431.2(XRCC2):c.527G>A (p.Cys176Tyr) rs753169131
NM_005431.2(XRCC2):c.539T>A (p.Leu180Ter) rs1064793297
NM_005431.2(XRCC2):c.544A>G (p.Lys182Glu) rs1064795338
NM_005431.2(XRCC2):c.545del (p.Lys182fs) rs587780129
NM_005431.2(XRCC2):c.570del (p.Leu191fs) rs879254270
NM_005431.2(XRCC2):c.596T>A (p.Met199Lys) rs149099078
NM_005431.2(XRCC2):c.650G>A (p.Cys217Tyr) rs879254219
NM_005431.2(XRCC2):c.651_652del (p.Cys217_Asp218delinsTer) rs746142129
NM_005431.2(XRCC2):c.678T>G (p.Tyr226Ter) rs143357617
NM_005431.2(XRCC2):c.713G>A (p.Arg238Lys) rs1064794162
NM_005431.2(XRCC2):c.730C>T (p.Gln244Ter) rs1064795954
NM_005431.2(XRCC2):c.767_768delinsAG (p.Val256Glu) rs1064794074
NM_005431.2(XRCC2):c.776_786delinsTAAAC (p.Cys259_Ser262delinsLeuAsn) rs587780131
NM_005431.2(XRCC2):c.808_810del (p.Phe270del) rs730882049
NM_005431.2(XRCC2):c.810dup (p.Ile271fs) rs730882049
NM_005431.2(XRCC2):c.811A>G (p.Ile271Val) rs587780132
NM_005431.2(XRCC2):c.820_821dup (p.Ser275fs) rs1554410400
NM_005431.2(XRCC2):c.821A>G (p.Glu274Gly) rs1064794061
NM_005431.2(XRCC2):c.826G>A (p.Gly276Arg) rs730882044
NM_005431.2(XRCC2):c.96del (p.Phe32fs) rs730882048

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