ClinVar Miner

List of variants in gene XRCC2 studied for not specified

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Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.*1T>C rs3218539 0.04983
NM_005431.2(XRCC2):c.40-10C>T rs3218472 0.01055
NM_005431.2(XRCC2):c.*1925A>C rs3218553 0.00784
NM_005431.2(XRCC2):c.808T>G (p.Phe270Val) rs145085742 0.00205
NM_005431.2(XRCC2):c.-50G>A rs139350845 0.00175
NM_005431.2(XRCC2):c.40-16T>C rs41274991 0.00141
NM_005431.2(XRCC2):c.613T>G (p.Ser205Ala) rs56103026 0.00017
NM_005431.2(XRCC2):c.283A>G (p.Ile95Val) rs140214637 0.00016
NM_005431.2(XRCC2):c.662T>C (p.Ile221Thr) rs3218537 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.678T>C (p.Tyr226=) rs143357617 0.00010
NM_005431.2(XRCC2):c.477C>T (p.Arg159=) rs202226401 0.00008
NM_005431.2(XRCC2):c.-14G>A rs750338805 0.00006
NM_005431.2(XRCC2):c.282A>G (p.Thr94=) rs376598559 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.252T>C (p.Asp84=) rs775563874 0.00004
NM_005431.2(XRCC2):c.669C>T (p.Tyr223=) rs374213093 0.00004
NM_005431.2(XRCC2):c.-15C>G rs1056607909 0.00003
NM_005431.2(XRCC2):c.-48G>A rs372428897 0.00002
NM_005431.2(XRCC2):c.225A>G (p.Glu75=) rs751651780 0.00002
NM_005431.2(XRCC2):c.264T>C (p.Asp88=) rs769940007 0.00002
NM_005431.2(XRCC2):c.582G>A (p.Thr194=) rs769829135 0.00002
NM_005431.2(XRCC2):c.591T>C (p.Thr197=) rs1252674838 0.00002
NM_005431.2(XRCC2):c.596T>C (p.Met199Thr) rs149099078 0.00002
NM_005431.2(XRCC2):c.-16C>T rs1229277495 0.00001
NM_005431.2(XRCC2):c.-17G>T rs760436323 0.00001
NM_005431.2(XRCC2):c.-42G>T rs1057521002 0.00001
NM_005431.2(XRCC2):c.140A>G (p.His47Arg) rs587780126 0.00001
NM_005431.2(XRCC2):c.223G>C (p.Glu75Gln) rs1327414828 0.00001
NM_005431.2(XRCC2):c.300A>G (p.Leu100=) rs146700851 0.00001
NM_005431.2(XRCC2):c.39+12C>T rs1057522924 0.00001
NM_005431.2(XRCC2):c.40-12T>C rs748238624 0.00001
NM_005431.2(XRCC2):c.432C>T (p.Cys144=) rs1290130026 0.00001
NM_005431.2(XRCC2):c.453G>A (p.Leu151=) rs1057522869 0.00001
NM_005431.2(XRCC2):c.456A>C (p.Ser152=) rs758944840 0.00001
NM_005431.2(XRCC2):c.492A>G (p.Glu164=) rs1167001769 0.00001
NM_005431.2(XRCC2):c.528T>C (p.Cys176=) rs765796648 0.00001
NM_005431.2(XRCC2):c.742C>G (p.Gln248Glu) rs190900560 0.00001
NM_005431.2(XRCC2):c.828G>A (p.Gly276=) rs1590129146 0.00001
NM_005431.2(XRCC2):c.842G>A (p.Ter281=) rs757510359 0.00001
NC_000007.13:g.(?_152343583)_(152346448_?)dup
NM_005431.2(XRCC2):c.-10C>T rs377067415
NM_005431.2(XRCC2):c.-27T>C rs1227014815
NM_005431.2(XRCC2):c.-29A>G rs1057523148
NM_005431.2(XRCC2):c.-30G>A rs371060479
NM_005431.2(XRCC2):c.-32_-31insC rs1064794758
NM_005431.2(XRCC2):c.-36A>C rs781776971
NM_005431.2(XRCC2):c.-5G>C rs1554413532
NM_005431.2(XRCC2):c.-6G>A rs773861668
NM_005431.2(XRCC2):c.121+3dup rs1064794394
NM_005431.2(XRCC2):c.121+8A>G rs1057523790
NM_005431.2(XRCC2):c.122-13A>T rs1057523098
NM_005431.2(XRCC2):c.122-3C>T rs730882046
NM_005431.2(XRCC2):c.155C>A (p.Thr52Lys) rs530663304
NM_005431.2(XRCC2):c.177T>C (p.Tyr59=) rs1554410569
NM_005431.2(XRCC2):c.21G>A (p.Arg7=) rs531499084
NM_005431.2(XRCC2):c.258C>T (p.His86=) rs1554410545
NM_005431.2(XRCC2):c.327A>G (p.Lys109=) rs1554410529
NM_005431.2(XRCC2):c.357C>T (p.Tyr119=) rs1057522562
NM_005431.2(XRCC2):c.39+11C>T rs1057521891
NM_005431.2(XRCC2):c.39+13G>C rs750274146
NM_005431.2(XRCC2):c.40-13C>A rs730882045
NM_005431.2(XRCC2):c.498G>C (p.Val166=) rs1057521124
NM_005431.2(XRCC2):c.502T>C (p.Leu168=) rs1057520526
NM_005431.2(XRCC2):c.545del (p.Lys182fs) rs587780129
NM_005431.2(XRCC2):c.549T>C (p.Leu183=) rs1554410454
NM_005431.2(XRCC2):c.711C>T (p.His237=) rs753368267
NM_005431.2(XRCC2):c.720T>C (p.Phe240=) rs1057521753
NM_005431.2(XRCC2):c.767_768delinsAG (p.Val256Glu) rs1064794074
NM_005431.2(XRCC2):c.776_786delinsTAAAC (p.Cys259_Ser262delinsLeuAsn) rs587780131

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