ClinVar Miner

List of variants in gene XRCC2 reported as likely pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.643C>T (p.Arg215Ter) rs143153871 0.00006
NM_005431.2(XRCC2):c.190C>T (p.Arg64Ter) rs151110146 0.00003
NM_005431.2(XRCC2):c.39+1G>A rs560785131 0.00001
NM_005431.2(XRCC2):c.39+2T>A rs758499439 0.00001
NM_005431.2(XRCC2):c.49C>T (p.Arg17Ter) rs750903875 0.00001
NM_005431.2(XRCC2):c.109dup (p.Ser37fs) rs1213272601
NM_005431.2(XRCC2):c.122-1G>T rs201836415
NM_005431.2(XRCC2):c.166_167del (p.Glu56fs)
NM_005431.2(XRCC2):c.175del (p.Tyr59fs)
NM_005431.2(XRCC2):c.240_243del (p.Phe80fs)
NM_005431.2(XRCC2):c.2T>C (p.Met1Thr) rs1064793295
NM_005431.2(XRCC2):c.350del (p.Leu117fs) rs764640893
NM_005431.2(XRCC2):c.350dup (p.Leu117fs) rs764640893
NM_005431.2(XRCC2):c.377T>A (p.Leu126Ter) rs1064794088
NM_005431.2(XRCC2):c.377T>G (p.Leu126Ter)
NM_005431.2(XRCC2):c.395C>A (p.Ser132Ter)
NM_005431.2(XRCC2):c.488dup (p.Glu164fs)
NM_005431.2(XRCC2):c.490_491del (p.Glu164fs) rs1590129487
NM_005431.2(XRCC2):c.609del (p.Ser204fs)
NM_005431.2(XRCC2):c.651_652del (p.Cys217_Asp218delinsTer) rs746142129
NM_005431.2(XRCC2):c.96del (p.Phe32fs) rs730882048

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