ClinVar Miner

List of variants in gene XRCC2 reported by Leiden Open Variation Database

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.808T>G (p.Phe270Val) rs145085742 0.00205
NM_005431.2(XRCC2):c.283A>G (p.Ile95Val) rs140214637 0.00016
NM_005431.2(XRCC2):c.620A>G (p.Glu207Gly) rs61762969 0.00013
NM_005431.2(XRCC2):c.354G>A (p.Val118=) rs558977371 0.00012
NM_005431.2(XRCC2):c.509A>C (p.Glu170Ala) rs778143946 0.00006
NM_005431.2(XRCC2):c.643C>T (p.Arg215Ter) rs143153871 0.00006
NM_005431.2(XRCC2):c.271C>T (p.Arg91Trp) rs730882043 0.00004
NM_005431.2(XRCC2):c.562C>T (p.Arg188Cys) rs139219364 0.00004
NM_005431.2(XRCC2):c.581C>T (p.Thr194Met) rs775565256 0.00004
NM_005431.2(XRCC2):c.772C>T (p.Arg258Cys) rs759300252 0.00002
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.223G>C (p.Glu75Gln) rs1327414828 0.00001
NM_005431.2(XRCC2):c.353T>C (p.Val118Ala) rs185815454 0.00001
NM_005431.2(XRCC2):c.359G>A (p.Cys120Tyr) rs1432878196 0.00001
NM_005431.2(XRCC2):c.398T>C (p.Leu133Pro) rs765276614 0.00001
NM_005431.2(XRCC2):c.490G>C (p.Glu164Gln) rs1215678098 0.00001
NM_005431.2(XRCC2):c.49C>T (p.Arg17Ter) rs750903875 0.00001
NM_005431.2(XRCC2):c.659A>T (p.Asp220Val) rs765021741 0.00001
NM_005431.2(XRCC2):c.714G>C (p.Arg238Ser) rs534746330 0.00001
NM_005431.2(XRCC2):c.742C>G (p.Gln248Glu) rs190900560 0.00001
NM_005431.2(XRCC2):c.-1G>A rs768232997
NM_005431.2(XRCC2):c.247dup (p.Thr83fs) rs2098027477
NM_005431.2(XRCC2):c.283A>C (p.Ile95Leu) rs140214637
NM_005431.2(XRCC2):c.350del (p.Leu117fs) rs764640893
NM_005431.2(XRCC2):c.46G>T (p.Ala16Ser) rs4987090
NM_005431.2(XRCC2):c.582G>T (p.Thr194=) rs769829135
NM_005431.2(XRCC2):c.595A>C (p.Met199Leu) rs2098027257
NM_005431.2(XRCC2):c.651_652del (p.Cys217_Asp218delinsTer) rs746142129
NM_005431.2(XRCC2):c.693G>T (p.Trp231Cys) rs1267462913

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