Xrcc2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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738 records found for search term Xrcc2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155740586	CV1809485	single nucleotide variant	NM_005431.2(XRCC2):c.-4G>A	Hereditary cancer-predisposing syndrome [RCV002343055]	uncertain significance	7	152676083	152676083	Human	1	name
155667003	CV1856794	single nucleotide variant	NM_005431.2(XRCC2):c.-2C>T	Hereditary cancer-predisposing syndrome [RCV002435626]	uncertain significance	7	152676081	152676081	Human	1	name
597680176	CV3731147	single nucleotide variant	NM_005431.2(XRCC2):c.*3T>C	not provided [RCV004998039]	uncertain significance	7	152648639	152648639	Human		name
13470851	CV474520	single nucleotide variant	NM_005431.2(XRCC2):c.*1T>C	Hereditary cancer-predisposing syndrome [RCV000563505]\|not provided [RCV001712589]\|not specified [RCV002476255]	benign	7	152648641	152648641	Human	1	name
13539548	CV501980	single nucleotide variant	NM_005431.2(XRCC2):c.-5G>C	Hereditary cancer-predisposing syndrome [RCV002358701]\|not specified [RCV000613434]	likely benign\|uncertain significance	7	152676084	152676084	Human	1	name
13535542	CV502318	single nucleotide variant	NM_005431.2(XRCC2):c.-6G>A	not specified [RCV000602418]	likely benign	7	152676085	152676085	Human		name
34889195	CV917958	single nucleotide variant	NM_005431.2(XRCC2):c.-1G>A	Hereditary cancer-predisposing syndrome [RCV002418657]\|XRCC2-related disorder [RCV003898192]\|not provided [RCV001194891]	likely benign\|uncertain significance	7	152676080	152676080	Human	1	name , trait , alternate_id
150484452	CV1280466	single nucleotide variant	NM_005431.2(XRCC2):c.*40G>C	not provided [RCV001715382]	benign	7	152648602	152648602	Human		name
8691669	CV141636	single nucleotide variant	NM_005431.2(XRCC2):c.-50G>A	not specified [RCV000126347]	benign	7	152676129	152676129	Human		name
12845093	CV369091	single nucleotide variant	NM_005431.2(XRCC2):c.-10C>T	not specified [RCV000439195]	likely benign	7	152676089	152676089	Human		name
12842768	CV369094	single nucleotide variant	NM_005431.2(XRCC2):c.-15C>G	not specified [RCV000435021]	likely benign	7	152676094	152676094	Human		name
12838390	CV369402	single nucleotide variant	NM_005431.2(XRCC2):c.-17G>T	not specified [RCV000426875]	likely benign	7	152676096	152676096	Human		name
12843275	CV369405	single nucleotide variant	NM_005431.2(XRCC2):c.-29A>G	not specified [RCV000435944]	likely benign	7	152676108	152676108	Human		name
12833000	CV369408	single nucleotide variant	NM_005431.2(XRCC2):c.-48G>A	not specified [RCV000417660]	benign	7	152676127	152676127	Human		name
12846234	CV369692	single nucleotide variant	NM_005431.2(XRCC2):c.-14G>A	not specified [RCV000441255]	likely benign	7	152676093	152676093	Human		name
12839629	CV369693	single nucleotide variant	NM_005431.2(XRCC2):c.-36A>C	not specified [RCV000429181]	likely benign	7	152676115	152676115	Human		name
12838791	CV369695	single nucleotide variant	NM_005431.2(XRCC2):c.-42G>T	not specified [RCV000427607]	likely benign	7	152676121	152676121	Human		name
13539181	CV501693	single nucleotide variant	NM_005431.2(XRCC2):c.-30G>A	not specified [RCV000612918]	likely benign	7	152676109	152676109	Human		name
13535648	CV502038	single nucleotide variant	NM_005431.2(XRCC2):c.-16C>T	not specified [RCV000607918]	likely benign	7	152676095	152676095	Human		name
13534964	CV502040	single nucleotide variant	NM_005431.2(XRCC2):c.-27T>C	not specified [RCV000607493]	likely benign	7	152676106	152676106	Human		name
127283391	CV1096193	deletion	NM_005431.2(XRCC2):c.40-6del	not provided [RCV001448509]	likely benign	7	152660788	152660788	Human		name
127233725	CV1096194	single nucleotide variant	NM_005431.2(XRCC2):c.39+9C>T	not provided [RCV001421851]	likely benign	7	152676032	152676032	Human		name
150332265	CV1171691	deletion	NM_005431.2(XRCC2):c.*228del	not provided [RCV001538954]	benign	7	152648414	152648414	Human		name
150484002	CV1263087	single nucleotide variant	NM_005431.2(XRCC2):c.*183C>T	not provided [RCV001686487]	benign	7	152648459	152648459	Human		name
155665000	CV1787175	single nucleotide variant	NM_005431.2(XRCC2):c.39+1G>T	Hereditary cancer-predisposing syndrome [RCV002366410]	uncertain significance	7	152676040	152676040	Human	1	name
155696161	CV1790642	single nucleotide variant	NM_005431.2(XRCC2):c.40-5A>G	Hereditary cancer-predisposing syndrome [RCV002321362]\|not provided [RCV003560957]	likely benign\|uncertain significance	7	152660787	152660787	Human	1	name
11345957	CV240018	single nucleotide variant	NM_005431.2(XRCC2):c.39+8C>G	Fanconi anemia complementation group U [RCV000988021]\|not provided [RCV000226875]	benign\|likely benign	7	152676033	152676033	Human	1	name
405115223	CV3019214	duplication	NM_005431.2(XRCC2):c.40-6dup	not provided [RCV003700112]	benign	7	152660787	152660788	Human		name
405196815	CV3146667	deletion	NM_005431.2(XRCC2):c.40-5del	not provided [RCV003844022]	likely benign	7	152660787	152660787	Human		name
12894841	CV407106	single nucleotide variant	NM_005431.2(XRCC2):c.39+1G>A	Hereditary cancer-predisposing syndrome [RCV001021395]	likely pathogenic	7	152676040	152676040	Human	1	name
25317901	CV815381	single nucleotide variant	NM_005431.2(XRCC2):c.39+5G>C	Hereditary cancer-predisposing syndrome [RCV001021397]\|not provided [RCV001316821]	uncertain significance	7	152676036	152676036	Human	1	name
25317899	CV815382	single nucleotide variant	NM_005431.2(XRCC2):c.39+2T>A	Hereditary cancer-predisposing syndrome [RCV001021396]\|not provided [RCV001341372]	likely pathogenic\|uncertain significance	7	152676039	152676039	Human	1	name
8691665	CV141632	single nucleotide variant	NM_005431.2(XRCC2):c.40-16T>C	Fanconi anemia complementation group U [RCV000988020]\|Hereditary cancer-predisposing syndrome [RCV000126343]\|not provided [RCV002055638]\|not specified [RCV000213080]	benign\|likely benign\|conflicting interpretations of pathogenicity	7	152660798	152660798	Human	2	name
151873159	CV1430153	single nucleotide variant	NM_005431.2(XRCC2):c.122-3C>A	not provided [RCV002035934]	uncertain significance	7	152649366	152649366	Human		name
152068112	CV1571121	single nucleotide variant	NM_005431.2(XRCC2):c.39+20G>A	not provided [RCV002129243]	likely benign	7	152676021	152676021	Human		name
152068004	CV1588961	single nucleotide variant	NM_005431.2(XRCC2):c.39+10G>T	not provided [RCV002209608]	likely benign	7	152676031	152676031	Human		name
152144688	CV1598768	single nucleotide variant	NM_005431.2(XRCC2):c.39+13G>A	not provided [RCV002157248]	likely benign	7	152676028	152676028	Human		name
9834890	CV180250	single nucleotide variant	NM_005431.2(XRCC2):c.122-3C>T	Hereditary cancer-predisposing syndrome [RCV002362853]\|not provided [RCV001055488]\|not specified [RCV000161113]	likely benign\|uncertain significance	7	152649366	152649366	Human	1	name
9834889	CV180253	single nucleotide variant	NM_005431.2(XRCC2):c.40-13C>A	not specified [RCV000161112]	likely benign	7	152660795	152660795	Human		name
10404627	CV207473	single nucleotide variant	NM_005431.2(XRCC2):c.*1925A>C	not provided [RCV004692803]\|not specified [RCV000194632]	uncertain significance	7	152646717	152646717	Human		name
155943481	CV2130045	single nucleotide variant	NM_005431.2(XRCC2):c.39+10G>A	not provided [RCV002971442]	likely benign	7	152676031	152676031	Human		name
11059934	CV226801	single nucleotide variant	NM_005431.2(XRCC2):c.40-10C>T	Fanconi anemia complementation group U [RCV003316162]\|not provided [RCV000857960]\|not specified [RCV000210512]	benign\|likely benign\|conflicting interpretations of pathogenicity	7	152660792	152660792	Human	1	name
12845120	CV369392	single nucleotide variant	NM_005431.2(XRCC2):c.121+8A>G	not provided [RCV002525457]\|not specified [RCV000439235]	likely benign	7	152660693	152660693	Human		name
12833194	CV369397	single nucleotide variant	NM_005431.2(XRCC2):c.39+11C>T	not specified [RCV000418054]	likely benign	7	152676030	152676030	Human		name
12835196	CV369688	single nucleotide variant	NM_005431.2(XRCC2):c.39+12C>T	not provided [RCV002522401]\|not specified [RCV000421271]	likely benign	7	152676029	152676029	Human		name
597680184	CV3731148	single nucleotide variant	NM_005431.2(XRCC2):c.122-5C>T	not provided [RCV004998040]	uncertain significance	7	152649368	152649368	Human		name
12899835	CV407100	duplication	NM_005431.2(XRCC2):c.121+3dup	not provided [RCV002056762]\|not specified [RCV000481059]	benign\|likely benign	7	152660692	152660693	Human		name
13539695	CV501690	single nucleotide variant	NM_005431.2(XRCC2):c.40-12T>C	not specified [RCV000613636]	likely benign	7	152660794	152660794	Human		name
13539456	CV502037	single nucleotide variant	NM_005431.2(XRCC2):c.39+13G>C	not provided [RCV002528717]\|not specified [RCV000613307]	likely benign	7	152676028	152676028	Human		name
25323146	CV815380	single nucleotide variant	NM_005431.2(XRCC2):c.122-1G>T	Hereditary cancer-predisposing syndrome [RCV001010393]	likely pathogenic	7	152649364	152649364	Human	1	name
150485164	CV1250170	single nucleotide variant	NM_005431.2(XRCC2):c.39+310G>C	not provided [RCV001673783]	benign	7	152675731	152675731	Human		name
150536168	CV1309165	single nucleotide variant	NM_005431.2(XRCC2):c.39+191C>T	not provided [RCV001759372]	likely benign	7	152675850	152675850	Human		name
152089987	CV1593963	single nucleotide variant	NM_005431.2(XRCC2):c.121+12A>C	not provided [RCV002171695]	likely benign	7	152660689	152660689	Human		name
156151183	CV1929302	single nucleotide variant	NM_005431.2(XRCC2):c.121+13A>C	not provided [RCV002624009]	likely benign	7	152660688	152660688	Human		name
156441552	CV1940934	single nucleotide variant	NM_005431.2(XRCC2):c.121+13A>G	not provided [RCV003111879]	likely benign	7	152660688	152660688	Human		name
405143016	CV3056091	single nucleotide variant	NM_005431.2(XRCC2):c.122-18T>G	not provided [RCV003725818]	likely benign	7	152649381	152649381	Human		name
12839491	CV369684	single nucleotide variant	NM_005431.2(XRCC2):c.122-13A>T	not specified [RCV000428914]	likely benign	7	152649376	152649376	Human		name
14738430	CV662862	single nucleotide variant	NM_005431.2(XRCC2):c.39+202C>T	not provided [RCV000839394]	benign	7	152675839	152675839	Human		name
150479784	CV1282384	single nucleotide variant	NM_005431.2(XRCC2):c.121+158T>G	not provided [RCV001714523]	benign	7	152660543	152660543	Human		name
150532753	CV1308099	single nucleotide variant	NM_005431.2(XRCC2):c.122-170A>G	not provided [RCV001753089]	likely benign	7	152649533	152649533	Human		name
11049842	CV225778	single nucleotide variant	NM_005431.2(XRCC2):c.39+4550T>C	Hereditary cancer-predisposing syndrome [RCV000209062]	likely benign	7	152671491	152671491	Human	1	name
11051099	CV225779	single nucleotide variant	NM_005431.2(XRCC2):c.122-840A>G	Hereditary cancer-predisposing syndrome [RCV000209267]	likely benign	7	152650203	152650203	Human	1	name
11051223	CV225780	single nucleotide variant	NM_005431.2(XRCC2):c.39+7425C>T	Hereditary cancer-predisposing syndrome [RCV000209610]	likely benign	7	152668616	152668616	Human	1	name
11049864	CV225781	single nucleotide variant	NM_005431.2(XRCC2):c.40-1611G>A	Hereditary cancer-predisposing syndrome [RCV000209105]	likely benign	7	152662393	152662393	Human	1	name
405226856	CV3039494	microsatellite	NM_005431.2(XRCC2):c.40-17CT[2]	not provided [RCV003710854]	likely benign	7	152660794	152660795	Human		name
11049929	CV225776	single nucleotide variant	NM_005431.2(XRCC2):c.122-4432A>G	Hereditary cancer-predisposing syndrome [RCV000209243]	likely benign	7	152653795	152653795	Human	1	name
11051243	CV225777	single nucleotide variant	NM_005431.2(XRCC2):c.122-4430G>T	Hereditary cancer-predisposing syndrome [RCV000209686]	likely benign	7	152653793	152653793	Human	1	name
12899917	CV407110	insertion	NM_005431.2(XRCC2):c.-32_-31insC	not specified [RCV000481243]	likely benign	7	152676110	152676111	Human		name
150486105	CV1280918	deletion	NM_005431.2(XRCC2):c.227_228del	not provided [RCV001715732]	benign	7	152648414	152648415	Human		name
15143089	CV779243	deletion	NM_005431.2(XRCC2):c.40-8_40-4del	not provided [RCV000966606]	likely benign	7	152660786	152660790	Human		name
127304705	CV1117712	microsatellite	NM_005431.2(XRCC2):c.40-10_40-8del	not provided [RCV001455038]	likely benign	7	152660790	152660792	Human		name
155731385	CV1825946	single nucleotide variant	NM_005431.2(XRCC2):c.9T>C (p.Ser3=)	Hereditary cancer-predisposing syndrome [RCV002383163]	likely benign	7	152676071	152676071	Human	1	name
405703767	CV3387055	single nucleotide variant	NM_005431.2(XRCC2):c.6T>C (p.Cys2=)	Hereditary cancer-predisposing syndrome [RCV004521382]	likely benign	7	152676074	152676074	Human	1	name
126918497	CV1044825	inversion	NM_005431.2(XRCC2):c.122-1899_627inv	not provided [RCV001361755]	uncertain significance	7	152648858	152651262	Human		name
155686530	CV1852618	single nucleotide variant	NM_005431.2(XRCC2):c.27G>A (p.Glu9=)	Hereditary cancer-predisposing syndrome [RCV002441557]	likely benign	7	152676053	152676053	Human	1	name
13536109	CV501979	single nucleotide variant	NM_005431.2(XRCC2):c.21G>A (p.Arg7=)	Hereditary cancer-predisposing syndrome [RCV002431792]\|not provided [RCV001490890]\|not specified [RCV000608525]	likely benign	7	152676059	152676059	Human	1	name
14708941	CV651680	insertion	NM_005431.2(XRCC2):c.122-1_122insATC	not provided [RCV000810706]	uncertain significance	7	152649363	152649364	Human		name
126749975	CV992217	single nucleotide variant	NM_005431.2(XRCC2):c.18T>C (p.His6=)	not provided [RCV001306748]	uncertain significance	7	152676062	152676062	Human		name
152084847	CV1622961	single nucleotide variant	NM_005431.2(XRCC2):c.72G>A (p.Leu24=)	not provided [RCV002113244]	likely benign	7	152660750	152660750	Human		name
155664239	CV1786479	single nucleotide variant	NM_005431.2(XRCC2):c.36C>A (p.Thr12=)	Hereditary cancer-predisposing syndrome [RCV002348894]	likely benign	7	152676044	152676044	Human	1	name
155678840	CV1786486	single nucleotide variant	NM_005431.2(XRCC2):c.36C>T (p.Thr12=)	Hereditary cancer-predisposing syndrome [RCV002353014]	likely benign	7	152676044	152676044	Human	1	name
155689651	CV1814518	single nucleotide variant	NM_005431.2(XRCC2):c.87A>C (p.Pro29=)	Hereditary cancer-predisposing syndrome [RCV002373691]	likely benign	7	152660735	152660735	Human	1	name
156013001	CV1880644	single nucleotide variant	NM_005431.2(XRCC2):c.3G>A (p.Met1Ile)	not provided [RCV003077201]	uncertain significance	7	152676077	152676077	Human		name
401863976	CV2763960	single nucleotide variant	NM_005431.2(XRCC2):c.33G>A (p.Gly11=)	Hereditary cancer-predisposing syndrome [RCV003344147]	likely benign	7	152676047	152676047	Human	1	name
401875677	CV2789128	single nucleotide variant	NM_005431.2(XRCC2):c.33G>T (p.Gly11=)	Hereditary cancer-predisposing syndrome [RCV003383128]	likely benign	7	152676047	152676047	Human	1	name
407465676	CV3493667	single nucleotide variant	NM_005431.2(XRCC2):c.42C>T (p.Leu14=)	Hereditary cancer-predisposing syndrome [RCV004688834]	likely benign	7	152660780	152660780	Human	1	name
597677740	CV3630468	single nucleotide variant	NM_005431.2(XRCC2):c.93G>A (p.Leu31=)	Hereditary cancer-predisposing syndrome [RCV004950995]	likely benign	7	152660729	152660729	Human	1	name
597955277	CV3757586	microsatellite	NM_005431.2(XRCC2):c.122-20_122-19del	not provided [RCV005080252]	likely benign	7	152649382	152649383	Human		name
12901538	CV407108	single nucleotide variant	NM_005431.2(XRCC2):c.7A>G (p.Ser3Gly)	Hereditary cancer-predisposing syndrome [RCV000708766]\|XRCC2-related disorder [RCV003401515]\|not provided [RCV000484929]	conflicting interpretations of pathogenicity\|uncertain significance	7	152676073	152676073	Human	1	name , trait , alternate_id
12894086	CV407109	single nucleotide variant	NM_005431.2(XRCC2):c.2T>C (p.Met1Thr)	Hereditary cancer-predisposing syndrome [RCV002435642]	pathogenic\|likely pathogenic	7	152676078	152676078	Human	1	name
15183236	CV766192	single nucleotide variant	NM_005431.2(XRCC2):c.30T>C (p.Ser10=)	Hereditary cancer-predisposing syndrome [RCV002320109]\|not provided [RCV000930546]	likely benign	7	152676050	152676050	Human	1	name
127319633	CV1138642	single nucleotide variant	NM_005431.2(XRCC2):c.144C>T (p.Gly48=)	Hereditary cancer-predisposing syndrome [RCV002388554]\|not provided [RCV001504100]	likely benign	7	152649341	152649341	Human	1	name
8691666	CV141633	single nucleotide variant	NM_005431.2(XRCC2):c.282A>G (p.Thr94=)	Hereditary cancer-predisposing syndrome [RCV000561837]\|not provided [RCV000858601]\|not specified [RCV000126344]	benign\|likely benign\|conflicting interpretations of pathogenicity	7	152649203	152649203	Human	1	name
152044803	CV1556014	single nucleotide variant	NM_005431.2(XRCC2):c.102T>C (p.Asp34=)	Hereditary cancer-predisposing syndrome [RCV004045603]\|not provided [RCV002206802]	likely benign\|conflicting interpretations of pathogenicity	7	152660720	152660720	Human	1	name
152106879	CV1591815	single nucleotide variant	NM_005431.2(XRCC2):c.270C>G (p.Leu90=)	Hereditary cancer-predisposing syndrome [RCV002427586]\|not provided [RCV002214932]	likely benign	7	152649215	152649215	Human	1	name
152042422	CV1603467	single nucleotide variant	NM_005431.2(XRCC2):c.147A>G (p.Pro49=)	Hereditary cancer-predisposing syndrome [RCV004681419]\|not provided [RCV002071193]	likely benign	7	152649338	152649338	Human	1	name
9834892	CV180252	deletion	NM_005431.2(XRCC2):c.96del (p.Phe32fs)	Breast carcinoma [RCV001640209]\|Hereditary cancer-predisposing syndrome [RCV000161115]\|not provided [RCV000254696]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	7	152660726	152660726	Human	3	name
155704462	CV1827933	single nucleotide variant	NM_005431.2(XRCC2):c.165A>T (p.Thr55=)	Hereditary cancer-predisposing syndrome [RCV002395081]	likely benign	7	152649320	152649320	Human	1	name
155732064	CV1835049	single nucleotide variant	NM_005431.2(XRCC2):c.17A>G (p.His6Arg)	Hereditary cancer-predisposing syndrome [RCV002407863]	likely benign\|uncertain significance	7	152676063	152676063	Human	1	name
155743335	CV1839370	single nucleotide variant	NM_005431.2(XRCC2):c.183A>C (p.Leu61=)	Hereditary cancer-predisposing syndrome [RCV002412789]	likely benign	7	152649302	152649302	Human	1	name
155685888	CV1841306	single nucleotide variant	NM_005431.2(XRCC2):c.237A>G (p.Leu79=)	Hereditary cancer-predisposing syndrome [RCV002457859]	likely benign	7	152649248	152649248	Human	1	name
155716614	CV1844721	single nucleotide variant	NM_005431.2(XRCC2):c.234C>T (p.Val78=)	Hereditary cancer-predisposing syndrome [RCV002448371]\|not provided [RCV003775204]	likely benign	7	152649251	152649251	Human	1	name
155717254	CV1844891	single nucleotide variant	NM_005431.2(XRCC2):c.235T>C (p.Leu79=)	Hereditary cancer-predisposing syndrome [RCV002448529]	likely benign	7	152649250	152649250	Human	1	name
155692728	CV1845774	single nucleotide variant	NM_005431.2(XRCC2):c.25G>A (p.Glu9Lys)	Hereditary cancer-predisposing syndrome [RCV002426230]	uncertain significance	7	152676055	152676055	Human	1	name
155692759	CV1845779	single nucleotide variant	NM_005431.2(XRCC2):c.25G>C (p.Glu9Gln)	Hereditary cancer-predisposing syndrome [RCV002426235]	uncertain significance	7	152676055	152676055	Human	1	name
155714718	CV1849252	single nucleotide variant	NM_005431.2(XRCC2):c.270C>T (p.Leu90=)	Hereditary cancer-predisposing syndrome [RCV002431170]	likely benign	7	152649215	152649215	Human	1	name
11345744	CV240017	single nucleotide variant	NM_005431.2(XRCC2):c.225A>G (p.Glu75=)	Hereditary cancer-predisposing syndrome [RCV001014960]\|not provided [RCV000791364]\|not specified [RCV000226124]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	7	152649260	152649260	Human	1	name
329389707	CV2467905	single nucleotide variant	NM_005431.2(XRCC2):c.141T>C (p.His47=)	Hereditary cancer-predisposing syndrome [RCV003216343]	likely benign	7	152649344	152649344	Human	1	name
329389512	CV2467906	single nucleotide variant	NM_005431.2(XRCC2):c.10G>A (p.Ala4Thr)	Hereditary cancer-predisposing syndrome [RCV003216344]	uncertain significance	7	152676070	152676070	Human	1	name
401899608	CV2790595	single nucleotide variant	NM_005431.2(XRCC2):c.105A>G (p.Glu35=)	Hereditary cancer-predisposing syndrome [RCV003377779]	uncertain significance	7	152660717	152660717	Human	1	name
401899611	CV2790598	single nucleotide variant	NM_005431.2(XRCC2):c.19A>G (p.Arg7Gly)	Hereditary cancer-predisposing syndrome [RCV003377782]	uncertain significance	7	152676061	152676061	Human	1	name
401899615	CV2790602	single nucleotide variant	NM_005431.2(XRCC2):c.159A>G (p.Gly53=)	Hereditary cancer-predisposing syndrome [RCV003377786]	likely benign	7	152649326	152649326	Human	1	name
405703525	CV3387025	single nucleotide variant	NM_005431.2(XRCC2):c.156A>G (p.Thr52=)	Hereditary cancer-predisposing syndrome [RCV004521352]	likely benign	7	152649329	152649329	Human	1	name
405703556	CV3387029	single nucleotide variant	NM_005431.2(XRCC2):c.22G>C (p.Ala8Pro)	Hereditary cancer-predisposing syndrome [RCV004521356]	uncertain significance	7	152676058	152676058	Human	1	name
405703563	CV3387030	single nucleotide variant	NM_005431.2(XRCC2):c.243T>A (p.Ile81=)	Hereditary cancer-predisposing syndrome [RCV004521357]	likely benign	7	152649242	152649242	Human	1	name
407456086	CV3493665	single nucleotide variant	NM_005431.2(XRCC2):c.16C>T (p.His6Tyr)	Hereditary cancer-predisposing syndrome [RCV004685818]	uncertain significance	7	152676064	152676064	Human	1	name
407456128	CV3493683	single nucleotide variant	NM_005431.2(XRCC2):c.135A>G (p.Glu45=)	Hereditary cancer-predisposing syndrome [RCV004685834]	likely benign	7	152649350	152649350	Human	1	name
597677769	CV3630471	single nucleotide variant	NM_005431.2(XRCC2):c.204C>G (p.Pro68=)	Hereditary cancer-predisposing syndrome [RCV004950998]	likely benign	7	152649281	152649281	Human	1	name
597677906	CV3630488	single nucleotide variant	NM_005431.2(XRCC2):c.201T>A (p.Leu67=)	Hereditary cancer-predisposing syndrome [RCV004951013]	likely benign	7	152649284	152649284	Human	1	name
597677937	CV3630491	single nucleotide variant	NM_005431.2(XRCC2):c.220C>T (p.Leu74=)	Hereditary cancer-predisposing syndrome [RCV004951016]	likely benign	7	152649265	152649265	Human	1	name
12838950	CV369675	single nucleotide variant	NM_005431.2(XRCC2):c.264T>C (p.Asp88=)	Hereditary cancer-predisposing syndrome [RCV001016210]\|not provided [RCV001488374]\|not specified [RCV000427914]	likely benign	7	152649221	152649221	Human	1	name
598241626	CV3933776	single nucleotide variant	NM_005431.2(XRCC2):c.210A>G (p.Ser70=)	Hereditary cancer-predisposing syndrome [RCV005296963]	likely benign	7	152649275	152649275	Human	1	name
598195611	CV3933785	single nucleotide variant	NM_005431.2(XRCC2):c.273G>T (p.Arg91=)	Hereditary cancer-predisposing syndrome [RCV005313358]	likely benign	7	152649212	152649212	Human	1	name
598241659	CV3933786	single nucleotide variant	NM_005431.2(XRCC2):c.23C>T (p.Ala8Val)	Hereditary cancer-predisposing syndrome [RCV005296969]	uncertain significance	7	152676057	152676057	Human	1	name
598241682	CV3933792	single nucleotide variant	NM_005431.2(XRCC2):c.153A>G (p.Gly51=)	Hereditary cancer-predisposing syndrome [RCV005296973]	likely benign	7	152649332	152649332	Human	1	name
13539142	CV501972	single nucleotide variant	NM_005431.2(XRCC2):c.252T>C (p.Asp84=)	Hereditary cancer-predisposing syndrome [RCV002431802]\|not provided [RCV003727777]\|not specified [RCV000612862]	likely benign	7	152649233	152649233	Human	1	name
13526964	CV501974	single nucleotide variant	NM_005431.2(XRCC2):c.177T>C (p.Tyr59=)	Hereditary cancer-predisposing syndrome [RCV002404631]\|not specified [RCV000604828]	likely benign	7	152649308	152649308	Human	1	name
13540069	CV502036	single nucleotide variant	NM_005431.2(XRCC2):c.258C>T (p.His86=)	Hereditary cancer-predisposing syndrome [RCV004024942]\|not provided [RCV003558461]\|not specified [RCV000614183]	likely benign	7	152649227	152649227	Human	1	name
15139264	CV687011	single nucleotide variant	NM_005431.2(XRCC2):c.246T>C (p.Asp82=)	not provided [RCV000864973]	likely benign	7	152649239	152649239	Human		name
15164477	CV736039	single nucleotide variant	NM_005431.2(XRCC2):c.144C>A (p.Gly48=)	Hereditary cancer-predisposing syndrome [RCV001011641]\|not provided [RCV000904010]	likely benign	7	152649341	152649341	Human	1	name
15131894	CV750532	single nucleotide variant	NM_005431.2(XRCC2):c.228A>G (p.Val76=)	not provided [RCV000920243]	likely benign	7	152649257	152649257	Human		name
15119633	CV782826	single nucleotide variant	NM_005431.2(XRCC2):c.117G>C (p.Val39=)	not provided [RCV000979150]	likely benign	7	152660705	152660705	Human		name
25328813	CV809016	single nucleotide variant	NM_005431.2(XRCC2):c.274C>T (p.Leu92=)	Hereditary cancer-predisposing syndrome [RCV001016491]	likely benign	7	152649211	152649211	Human	1	name
25328636	CV809018	single nucleotide variant	NM_005431.2(XRCC2):c.261T>C (p.Phe87=)	Hereditary cancer-predisposing syndrome [RCV001016124]\|not provided [RCV001393493]	likely benign	7	152649224	152649224	Human	1	name
25329195	CV809025	single nucleotide variant	NM_005431.2(XRCC2):c.108T>C (p.Asp36=)	Hereditary cancer-predisposing syndrome [RCV001017245]	likely benign	7	152660714	152660714	Human	1	name
126758618	CV992216	single nucleotide variant	NM_005431.2(XRCC2):c.22G>A (p.Ala8Thr)	Hereditary cancer-predisposing syndrome [RCV004951462]\|not provided [RCV001299241]	likely benign\|uncertain significance	7	152676058	152676058	Human	1	name
126758022	CV992218	single nucleotide variant	NM_005431.2(XRCC2):c.10G>T (p.Ala4Ser)	Hereditary cancer-predisposing syndrome [RCV003166760]\|not provided [RCV001308592]	uncertain significance	7	152676070	152676070	Human	1	name
126727624	CV1007368	single nucleotide variant	NM_005431.2(XRCC2):c.85C>T (p.Pro29Ser)	not provided [RCV001312321]	uncertain significance	7	152660737	152660737	Human		name
126762456	CV1027915	single nucleotide variant	NM_005431.2(XRCC2):c.86C>T (p.Pro29Leu)	not provided [RCV001340977]	uncertain significance	7	152660736	152660736	Human		name
126747545	CV1027916	single nucleotide variant	NM_005431.2(XRCC2):c.39G>C (p.Glu13Asp)	Hereditary cancer-predisposing syndrome [RCV002357175]\|not provided [RCV001337487]	uncertain significance	7	152676041	152676041	Human	1	name
126911591	CV1044832	single nucleotide variant	NM_005431.2(XRCC2):c.91C>A (p.Leu31Met)	not provided [RCV001369291]	uncertain significance	7	152660731	152660731	Human		name
127242894	CV1096192	single nucleotide variant	NM_005431.2(XRCC2):c.609G>A (p.Ser203=)	Hereditary cancer-predisposing syndrome [RCV002358945]\|not provided [RCV001423835]	likely benign	7	152648876	152648876	Human	1	name
127336271	CV1117711	single nucleotide variant	NM_005431.2(XRCC2):c.801A>G (p.Lys267=)	not provided [RCV001474856]	likely benign	7	152648684	152648684	Human		name
150473760	CV1217684	single nucleotide variant	NM_005431.2(XRCC2):c.726C>T (p.Ser242=)	Hereditary cancer-predisposing syndrome [RCV002386490]\|not provided [RCV001615695]	benign\|likely benign	7	152648759	152648759	Human	1	name
151733526	CV1386745	duplication	NM_005431.2(XRCC2):c.109dup (p.Ser37fs)	Hereditary cancer-predisposing syndrome [RCV002458740]\|not provided [RCV001911121]	likely pathogenic\|uncertain significance	7	152660712	152660713	Human	1	name
8691667	CV141634	single nucleotide variant	NM_005431.2(XRCC2):c.354G>A (p.Val118=)	Hereditary cancer-predisposing syndrome [RCV000566518]\|XRCC2-related disorder [RCV003975115]\|not provided [RCV000858752]\|not specified [RCV000126345]	benign\|likely benign	7	152649131	152649131	Human	1	name , trait , alternate_id
8691668	CV141635	single nucleotide variant	NM_005431.2(XRCC2):c.477C>T (p.Arg159=)	Hereditary cancer-predisposing syndrome [RCV000575359]\|XRCC2-related disorder [RCV003965049]\|not provided [RCV000859248]\|not specified [RCV000126346]	benign\|likely benign\|conflicting interpretations of pathogenicity	7	152649008	152649008	Human	1	name , trait , alternate_id
151886938	CV1471843	single nucleotide variant	NM_005431.2(XRCC2):c.41T>A (p.Leu14His)	Hereditary cancer-predisposing syndrome [RCV002331571]\|not provided [RCV002000782]	uncertain significance	7	152660781	152660781	Human	1	name
151729144	CV1515805	single nucleotide variant	NM_005431.2(XRCC2):c.80T>C (p.Ile27Thr)	Hereditary cancer-predisposing syndrome [RCV002423209]\|not provided [RCV001984011]	uncertain significance	7	152660742	152660742	Human	1	name
152081738	CV1546808	single nucleotide variant	NM_005431.2(XRCC2):c.702G>A (p.Leu234=)	not provided [RCV002130904]	likely benign	7	152648783	152648783	Human		name
152174610	CV1602156	single nucleotide variant	NM_005431.2(XRCC2):c.723C>T (p.Phe241=)	not provided [RCV002144495]	likely benign	7	152648762	152648762	Human		name
152148981	CV1616673	single nucleotide variant	NM_005431.2(XRCC2):c.651T>C (p.Cys217=)	Hereditary cancer-predisposing syndrome [RCV002363717]\|not provided [RCV002201673]	likely benign	7	152648834	152648834	Human	1	name
152131295	CV1631105	single nucleotide variant	NM_005431.2(XRCC2):c.702G>C (p.Leu234=)	Hereditary cancer-predisposing syndrome [RCV002363661]\|not provided [RCV002119122]	likely benign	7	152648783	152648783	Human	1	name
152165938	CV1661092	single nucleotide variant	NM_005431.2(XRCC2):c.654T>C (p.Asp218=)	Hereditary cancer-predisposing syndrome [RCV002363664]\|not provided [RCV002124124]	likely benign	7	152648831	152648831	Human	1	name
155702052	CV1785321	single nucleotide variant	NM_005431.2(XRCC2):c.321A>C (p.Ile107=)	Hereditary cancer-predisposing syndrome [RCV002445460]	likely benign	7	152649164	152649164	Human	1	name
155732275	CV1785703	single nucleotide variant	NM_005431.2(XRCC2):c.336G>A (p.Leu112=)	Hereditary cancer-predisposing syndrome [RCV002451723]	likely benign	7	152649149	152649149	Human	1	name
155726355	CV1791056	single nucleotide variant	NM_005431.2(XRCC2):c.420C>T (p.His140=)	Hereditary cancer-predisposing syndrome [RCV002327934]	likely benign	7	152649065	152649065	Human	1	name
155703350	CV1791505	single nucleotide variant	NM_005431.2(XRCC2):c.441T>C (p.Ile147=)	Hereditary cancer-predisposing syndrome [RCV002333894]	likely benign	7	152649044	152649044	Human	1	name
155673061	CV1792167	single nucleotide variant	NM_005431.2(XRCC2):c.32G>T (p.Gly11Val)	Hereditary cancer-predisposing syndrome [RCV002454686]	uncertain significance	7	152676048	152676048	Human	1	name
155666451	CV1793121	single nucleotide variant	NM_005431.2(XRCC2):c.363T>C (p.Ser121=)	Hereditary cancer-predisposing syndrome [RCV002452428]	likely benign	7	152649122	152649122	Human	1	name
155672131	CV1793251	single nucleotide variant	NM_005431.2(XRCC2):c.378A>G (p.Leu126=)	Hereditary cancer-predisposing syndrome [RCV002351191]	likely benign	7	152649107	152649107	Human	1	name
155676435	CV1796139	single nucleotide variant	NM_005431.2(XRCC2):c.35C>A (p.Thr12Asn)	Hereditary cancer-predisposing syndrome [RCV002455179]	uncertain significance	7	152676045	152676045	Human	1	name
155676460	CV1796144	single nucleotide variant	NM_005431.2(XRCC2):c.35C>T (p.Thr12Ile)	Hereditary cancer-predisposing syndrome [RCV002455183]	uncertain significance	7	152676045	152676045	Human	1	name
155735000	CV1797865	single nucleotide variant	NM_005431.2(XRCC2):c.429C>T (p.Leu143=)	Hereditary cancer-predisposing syndrome [RCV002330271]	likely benign	7	152649056	152649056	Human	1	name
155728898	CV1798407	single nucleotide variant	NM_005431.2(XRCC2):c.447T>C (p.Asp149=)	Hereditary cancer-predisposing syndrome [RCV002328558]	likely benign	7	152649038	152649038	Human	1	name
155724169	CV1799396	single nucleotide variant	NM_005431.2(XRCC2):c.516T>A (p.Thr172=)	Hereditary cancer-predisposing syndrome [RCV002338388]	likely benign	7	152648969	152648969	Human	1	name
155682668	CV1801028	single nucleotide variant	NM_005431.2(XRCC2):c.627T>C (p.Pro209=)	Hereditary cancer-predisposing syndrome [RCV002353922]	likely benign	7	152648858	152648858	Human	1	name
155683452	CV1801388	single nucleotide variant	NM_005431.2(XRCC2):c.633T>C (p.His211=)	Hereditary cancer-predisposing syndrome [RCV002354040]	likely benign	7	152648852	152648852	Human	1	name
155745899	CV1803057	single nucleotide variant	NM_005431.2(XRCC2):c.53T>C (p.Leu18Pro)	Hereditary cancer-predisposing syndrome [RCV002347266]	uncertain significance	7	152660769	152660769	Human	1	name
155744053	CV1803294	single nucleotide variant	NM_005431.2(XRCC2):c.564C>T (p.Arg188=)	Hereditary cancer-predisposing syndrome [RCV002345170]	likely benign	7	152648921	152648921	Human	1	name
155746193	CV1803465	single nucleotide variant	NM_005431.2(XRCC2):c.567G>A (p.Leu189=)	Hereditary cancer-predisposing syndrome [RCV002347414]	likely benign	7	152648918	152648918	Human	1	name
155738648	CV1805220	single nucleotide variant	NM_005431.2(XRCC2):c.459T>A (p.Ala153=)	Hereditary cancer-predisposing syndrome [RCV002342344]	likely benign	7	152649026	152649026	Human	1	name
155720500	CV1805397	single nucleotide variant	NM_005431.2(XRCC2):c.480C>T (p.Val160=)	Hereditary cancer-predisposing syndrome [RCV002337934]	likely benign	7	152649005	152649005	Human	1	name
155743481	CV1806805	single nucleotide variant	NM_005431.2(XRCC2):c.55G>A (p.Glu19Lys)	Hereditary cancer-predisposing syndrome [RCV002344886]\|not provided [RCV003096805]	uncertain significance	7	152660767	152660767	Human	1	name
155679917	CV1807089	single nucleotide variant	NM_005431.2(XRCC2):c.585A>T (p.Thr195=)	Hereditary cancer-predisposing syndrome [RCV002353378]	likely benign	7	152648900	152648900	Human	1	name
155712757	CV1808018	single nucleotide variant	NM_005431.2(XRCC2):c.645A>C (p.Arg215=)	Hereditary cancer-predisposing syndrome [RCV002361879]	likely benign	7	152648840	152648840	Human	1	name
155713698	CV1808199	single nucleotide variant	NM_005431.2(XRCC2):c.648G>A (p.Leu216=)	Hereditary cancer-predisposing syndrome [RCV002361996]	likely benign	7	152648837	152648837	Human	1	name
155690089	CV1808205	single nucleotide variant	NM_005431.2(XRCC2):c.648G>T (p.Leu216=)	Hereditary cancer-predisposing syndrome [RCV002356244]	likely benign	7	152648837	152648837	Human	1	name
155729595	CV1808421	single nucleotide variant	NM_005431.2(XRCC2):c.44T>C (p.Leu15Pro)	Hereditary cancer-predisposing syndrome [RCV002328695]	uncertain significance	7	152660778	152660778	Human	1	name
155736551	CV1808907	single nucleotide variant	NM_005431.2(XRCC2):c.474C>T (p.Asp158=)	Hereditary cancer-predisposing syndrome [RCV002330617]	likely benign	7	152649011	152649011	Human	1	name
155719310	CV1809101	single nucleotide variant	NM_005431.2(XRCC2):c.477C>A (p.Arg159=)	Hereditary cancer-predisposing syndrome [RCV002337766]	likely benign	7	152649008	152649008	Human	1	name
155734938	CV1809702	single nucleotide variant	NM_005431.2(XRCC2):c.522G>A (p.Arg174=)	Hereditary cancer-predisposing syndrome [RCV002340847]	likely benign	7	152648963	152648963	Human	1	name
155674279	CV1810117	single nucleotide variant	NM_005431.2(XRCC2):c.549T>G (p.Leu183=)	Hereditary cancer-predisposing syndrome [RCV002351618]	likely benign	7	152648936	152648936	Human	1	name
155675469	CV1810297	single nucleotide variant	NM_005431.2(XRCC2):c.552A>C (p.Val184=)	Hereditary cancer-predisposing syndrome [RCV002351798]	likely benign	7	152648933	152648933	Human	1	name
155675527	CV1810306	single nucleotide variant	NM_005431.2(XRCC2):c.552A>T (p.Val184=)	Hereditary cancer-predisposing syndrome [RCV002351807]	likely benign	7	152648933	152648933	Human	1	name
155674508	CV1811423	single nucleotide variant	NM_005431.2(XRCC2):c.636C>T (p.Ala212=)	Hereditary cancer-predisposing syndrome [RCV002369073]	likely benign	7	152648849	152648849	Human	1	name
155698151	CV1811908	single nucleotide variant	NM_005431.2(XRCC2):c.660C>T (p.Asp220=)	Hereditary cancer-predisposing syndrome [RCV002375855]	likely benign	7	152648825	152648825	Human	1	name
155707121	CV1812272	single nucleotide variant	NM_005431.2(XRCC2):c.690A>G (p.Ala230=)	Hereditary cancer-predisposing syndrome [RCV002378077]\|not provided [RCV003560979]	likely benign	7	152648795	152648795	Human	1	name
155747358	CV1813592	single nucleotide variant	NM_005431.2(XRCC2):c.792T>C (p.Ser264=)	Hereditary cancer-predisposing syndrome [RCV002416788]	likely benign	7	152648693	152648693	Human	1	name
155742882	CV1814108	single nucleotide variant	NM_005431.2(XRCC2):c.834A>G (p.Glu278=)	Hereditary cancer-predisposing syndrome [RCV002412586]	likely benign	7	152648651	152648651	Human	1	name
155677553	CV1815103	single nucleotide variant	NM_005431.2(XRCC2):c.681C>T (p.Leu227=)	Hereditary cancer-predisposing syndrome [RCV002369576]	likely benign	7	152648804	152648804	Human	1	name
155707969	CV1817166	single nucleotide variant	NM_005431.2(XRCC2):c.828G>C (p.Gly276=)	Hereditary cancer-predisposing syndrome [RCV002430279]	likely benign	7	152648657	152648657	Human	1	name
155705006	CV1824015	single nucleotide variant	NM_005431.2(XRCC2):c.840T>C (p.Cys280=)	Hereditary cancer-predisposing syndrome [RCV002445866]	likely benign	7	152648645	152648645	Human	1	name
155674048	CV1825685	single nucleotide variant	NM_005431.2(XRCC2):c.97G>A (p.Ala33Thr)	Hereditary cancer-predisposing syndrome [RCV002387234]\|not provided [RCV003103619]	uncertain significance	7	152660725	152660725	Human	1	name
155701869	CV1838204	deletion	NM_005431.2(XRCC2):c.175del (p.Tyr59fs)	Hereditary cancer-predisposing syndrome [RCV002401648]	likely pathogenic	7	152649310	152649310	Human	1	name
156087103	CV1899040	single nucleotide variant	NM_005431.2(XRCC2):c.31G>A (p.Gly11Arg)	not provided [RCV003080077]	uncertain significance	7	152676049	152676049	Human		name
156146473	CV2188316	single nucleotide variant	NM_005431.2(XRCC2):c.675T>G (p.Pro225=)	Hereditary cancer-predisposing syndrome [RCV003348984]\|not provided [RCV003056377]	likely benign	7	152648810	152648810	Human	1	name
329383963	CV2432426	single nucleotide variant	NM_005431.2(XRCC2):c.81A>G (p.Ile27Met)	Hereditary cancer-predisposing syndrome [RCV003176494]	uncertain significance	7	152660741	152660741	Human	1	name
401754878	CV2717565	single nucleotide variant	NM_005431.2(XRCC2):c.372C>T (p.Thr124=)	Hereditary cancer-predisposing syndrome [RCV003296716]	likely benign	7	152649113	152649113	Human	1	name
401774749	CV2728259	single nucleotide variant	NM_005431.2(XRCC2):c.88A>G (p.Asn30Asp)	Hereditary cancer-predisposing syndrome [RCV003305384]	uncertain significance	7	152660734	152660734	Human	1	name
401774757	CV2728261	single nucleotide variant	NM_005431.2(XRCC2):c.71T>C (p.Leu24Ser)	Hereditary cancer-predisposing syndrome [RCV003305386]\|not provided [RCV003777120]	uncertain significance	7	152660751	152660751	Human	1	name
401869974	CV2760733	single nucleotide variant	NM_005431.2(XRCC2):c.612C>T (p.Ser204=)	Hereditary cancer-predisposing syndrome [RCV003361069]\|not provided [RCV003730533]	likely benign	7	152648873	152648873	Human	1	name
401869716	CV2764102	single nucleotide variant	NM_005431.2(XRCC2):c.636C>G (p.Ala212=)	Hereditary cancer-predisposing syndrome [RCV003360985]\|not provided [RCV003708777]	likely benign	7	152648849	152648849	Human	1	name
401899613	CV2790600	deletion	NM_005431.2(XRCC2):c.190del (p.Arg64fs)	Hereditary cancer-predisposing syndrome [RCV003377784]	pathogenic	7	152649295	152649295	Human	1	name
401899618	CV2790605	single nucleotide variant	NM_005431.2(XRCC2):c.65G>T (p.Ser22Ile)	Hereditary cancer-predisposing syndrome [RCV003377789]	uncertain significance	7	152660757	152660757	Human	1	name
401899619	CV2790606	single nucleotide variant	NM_005431.2(XRCC2):c.64A>C (p.Ser22Arg)	Hereditary cancer-predisposing syndrome [RCV003377790]	uncertain significance	7	152660758	152660758	Human	1	name
405239514	CV2993355	duplication	NM_005431.2(XRCC2):c.280dup (p.Thr94fs)	not provided [RCV003718885]	uncertain significance	7	152649204	152649205	Human		name
405140682	CV3045459	single nucleotide variant	NM_005431.2(XRCC2):c.793T>C (p.Leu265=)	not provided [RCV003725539]	likely benign	7	152648692	152648692	Human		name
405027999	CV3076163	deletion	NM_005431.2(XRCC2):c.223del (p.Glu75fs)	not provided [RCV003738929]	uncertain significance	7	152649262	152649262	Human		name
405703593	CV3387034	single nucleotide variant	NM_005431.2(XRCC2):c.369C>T (p.Ser123=)	Hereditary cancer-predisposing syndrome [RCV004521361]	likely benign	7	152649116	152649116	Human	1	name
405703662	CV3387042	single nucleotide variant	NM_005431.2(XRCC2):c.46G>C (p.Ala16Pro)	Hereditary cancer-predisposing syndrome [RCV004521369]	uncertain significance	7	152660776	152660776	Human	1	name
405703669	CV3387043	single nucleotide variant	NM_005431.2(XRCC2):c.486A>G (p.Gly162=)	Hereditary cancer-predisposing syndrome [RCV004521370]	likely benign	7	152648999	152648999	Human	1	name
405703746	CV3387053	single nucleotide variant	NM_005431.2(XRCC2):c.657G>A (p.Val219=)	Hereditary cancer-predisposing syndrome [RCV004521380]	likely benign	7	152648828	152648828	Human	1	name
405703803	CV3387059	single nucleotide variant	NM_005431.2(XRCC2):c.73A>G (p.Lys25Glu)	Hereditary cancer-predisposing syndrome [RCV004521386]	uncertain significance	7	152660749	152660749	Human	1	name
405703855	CV3387065	single nucleotide variant	NM_005431.2(XRCC2):c.83A>G (p.Glu28Gly)	Hereditary cancer-predisposing syndrome [RCV004521392]	uncertain significance	7	152660739	152660739	Human	1	name
405703866	CV3387066	single nucleotide variant	NM_005431.2(XRCC2):c.85C>A (p.Pro29Thr)	Hereditary cancer-predisposing syndrome [RCV004521393]	uncertain significance	7	152660737	152660737	Human	1	name
405703875	CV3387067	single nucleotide variant	NM_005431.2(XRCC2):c.98C>T (p.Ala33Val)	Hereditary cancer-predisposing syndrome [RCV004521394]	uncertain significance	7	152660724	152660724	Human	1	name
407465669	CV3493663	single nucleotide variant	NM_005431.2(XRCC2):c.618A>T (p.Ser206=)	Hereditary cancer-predisposing syndrome [RCV004688832]	likely benign	7	152648867	152648867	Human	1	name
407456091	CV3493668	single nucleotide variant	NM_005431.2(XRCC2):c.52C>G (p.Leu18Val)	Hereditary cancer-predisposing syndrome [RCV004685820]	uncertain significance	7	152660770	152660770	Human	1	name
407456118	CV3493678	single nucleotide variant	NM_005431.2(XRCC2):c.747C>T (p.Ser249=)	Hereditary cancer-predisposing syndrome [RCV004685830]	likely benign	7	152648738	152648738	Human	1	name
407456123	CV3493680	single nucleotide variant	NM_005431.2(XRCC2):c.786T>C (p.Ser262=)	Hereditary cancer-predisposing syndrome [RCV004685832]	likely benign	7	152648699	152648699	Human	1	name
407456126	CV3493682	single nucleotide variant	NM_005431.2(XRCC2):c.57A>T (p.Glu19Asp)	Hereditary cancer-predisposing syndrome [RCV004685833]	uncertain significance	7	152660765	152660765	Human	1	name
597677731	CV3630466	single nucleotide variant	NM_005431.2(XRCC2):c.714G>A (p.Arg238=)	Hereditary cancer-predisposing syndrome [RCV004950994]	likely benign	7	152648771	152648771	Human	1	name
597677749	CV3630469	single nucleotide variant	NM_005431.2(XRCC2):c.43C>T (p.Leu15Phe)	Hereditary cancer-predisposing syndrome [RCV004950996]	uncertain significance	7	152660779	152660779	Human	1	name
597677897	CV3630487	single nucleotide variant	NM_005431.2(XRCC2):c.76G>A (p.Glu26Lys)	Hereditary cancer-predisposing syndrome [RCV004951012]	uncertain significance	7	152660746	152660746	Human	1	name
597677973	CV3630496	single nucleotide variant	NM_005431.2(XRCC2):c.315A>G (p.Glu105=)	Hereditary cancer-predisposing syndrome [RCV004951020]	likely benign	7	152649170	152649170	Human	1	name
12847948	CV369073	single nucleotide variant	NM_005431.2(XRCC2):c.720T>C (p.Phe240=)	Hereditary cancer-predisposing syndrome [RCV001026164]\|not specified [RCV000444400]	likely benign	7	152648765	152648765	Human	1	name
12845651	CV369079	single nucleotide variant	NM_005431.2(XRCC2):c.669C>T (p.Tyr223=)	Hereditary cancer-predisposing syndrome [RCV000568750]\|XRCC2-related disorder [RCV003892129]\|not provided [RCV001504041]\|not specified [RCV000440208]	likely benign	7	152648816	152648816	Human	1	name , trait , alternate_id
12843668	CV369080	single nucleotide variant	NM_005431.2(XRCC2):c.582G>A (p.Thr194=)	Hereditary cancer-predisposing syndrome [RCV002356566]\|not provided [RCV000951938]\|not specified [RCV000436621]	likely benign	7	152648903	152648903	Human	1	name
12845452	CV369082	single nucleotide variant	NM_005431.2(XRCC2):c.528T>C (p.Cys176=)	Hereditary cancer-predisposing syndrome [RCV001023873]\|XRCC2-related disorder [RCV003970134]\|not provided [RCV000909133]\|not specified [RCV000439836]	likely benign	7	152648957	152648957	Human	1	name , trait , alternate_id
12845009	CV369378	single nucleotide variant	NM_005431.2(XRCC2):c.678T>C (p.Tyr226=)	Hereditary cancer-predisposing syndrome [RCV000572684]\|not provided [RCV000858986]\|not specified [RCV000439030]	benign\|likely benign\|conflicting interpretations of pathogenicity	7	152648807	152648807	Human	1	name
12841764	CV369383	single nucleotide variant	NM_005431.2(XRCC2):c.498G>C (p.Val166=)	Hereditary cancer-predisposing syndrome [RCV002339008]\|not provided [RCV000964718]\|not specified [RCV000433155]	likely benign	7	152648987	152648987	Human	1	name
12833669	CV369389	single nucleotide variant	NM_005431.2(XRCC2):c.357C>T (p.Tyr119=)	not specified [RCV000418948]	likely benign	7	152649128	152649128	Human		name
12835281	CV369666	single nucleotide variant	NM_005431.2(XRCC2):c.711C>T (p.His237=)	Hereditary cancer-predisposing syndrome [RCV004022302]\|not specified [RCV000421404]	likely benign	7	152648774	152648774	Human	1	name
12846767	CV369668	single nucleotide variant	NM_005431.2(XRCC2):c.453G>A (p.Leu151=)	Hereditary cancer-predisposing syndrome [RCV002339062]\|not provided [RCV001492268]\|not specified [RCV000442256]	likely benign	7	152649032	152649032	Human	1	name
12840443	CV369674	single nucleotide variant	NM_005431.2(XRCC2):c.300A>G (p.Leu100=)	Fanconi anemia complementation group U [RCV003316531]\|Hereditary cancer-predisposing syndrome [RCV001018019]\|not provided [RCV000870228]\|not specified [RCV000430717]	benign\|likely benign	7	152649185	152649185	Human	2	name
12833079	CV371066	single nucleotide variant	NM_005431.2(XRCC2):c.842G>A (p.Ter281=)	Hereditary cancer-predisposing syndrome [RCV002446748]\|not provided [RCV001035582]\|not specified [RCV000417829]	likely benign\|uncertain significance	7	152648643	152648643	Human	1	name
12844120	CV371069	single nucleotide variant	NM_005431.2(XRCC2):c.502T>C (p.Leu168=)	Hereditary cancer-predisposing syndrome [RCV002339002]\|not specified [RCV000437430]	likely benign	7	152648983	152648983	Human	1	name
12833923	CV371071	single nucleotide variant	NM_005431.2(XRCC2):c.456A>C (p.Ser152=)	Hereditary cancer-predisposing syndrome [RCV000567095]\|not provided [RCV000878055]\|not specified [RCV000419422]	likely benign	7	152649029	152649029	Human	1	name
597832532	CV3760214	single nucleotide variant	NM_005431.2(XRCC2):c.29C>G (p.Ser10Cys)	Hereditary cancer-predisposing syndrome [RCV005303485]\|not provided [RCV005084957]	uncertain significance	7	152676051	152676051	Human	1	name
597907784	CV3830139	single nucleotide variant	NM_005431.2(XRCC2):c.582G>C (p.Thr194=)	not provided [RCV005182709]	likely benign	7	152648903	152648903	Human		name
598183267	CV3933772	single nucleotide variant	NM_005431.2(XRCC2):c.609G>C (p.Ser203=)	Hereditary cancer-predisposing syndrome [RCV005311374]	likely benign	7	152648876	152648876	Human	1	name
598241609	CV3933773	single nucleotide variant	NM_005431.2(XRCC2):c.86C>A (p.Pro29Gln)	Hereditary cancer-predisposing syndrome [RCV005296960]	uncertain significance	7	152660736	152660736	Human	1	name
598241642	CV3933779	single nucleotide variant	NM_005431.2(XRCC2):c.606C>G (p.Ala202=)	Hereditary cancer-predisposing syndrome [RCV005296966]	likely benign	7	152648879	152648879	Human	1	name
598241649	CV3933781	single nucleotide variant	NM_005431.2(XRCC2):c.97G>T (p.Ala33Ser)	Hereditary cancer-predisposing syndrome [RCV005296967]	uncertain significance	7	152660725	152660725	Human	1	name
598241655	CV3933783	single nucleotide variant	NM_005431.2(XRCC2):c.345T>C (p.Phe115=)	Hereditary cancer-predisposing syndrome [RCV005296968]	likely benign	7	152649140	152649140	Human	1	name
598241669	CV3933789	single nucleotide variant	NM_005431.2(XRCC2):c.73A>C (p.Lys25Gln)	Hereditary cancer-predisposing syndrome [RCV005296971]	uncertain significance	7	152660749	152660749	Human	1	name
12897319	CV395899	single nucleotide variant	NM_005431.2(XRCC2):c.97G>C (p.Ala33Pro)	Fanconi anemia complementation group U [RCV001292718]\|Hereditary cancer-predisposing syndrome [RCV001019768]\|not provided [RCV000460519]	uncertain significance	7	152660725	152660725	Human	2	name
12901343	CV407103	single nucleotide variant	NM_005431.2(XRCC2):c.91C>G (p.Leu31Val)	Hereditary cancer-predisposing syndrome [RCV001018997]\|not provided [RCV000484446]	uncertain significance	7	152660731	152660731	Human	1	name
12899674	CV407104	single nucleotide variant	NM_005431.2(XRCC2):c.50G>A (p.Arg17Gln)	Hereditary cancer-predisposing syndrome [RCV001023541]\|not provided [RCV000480720]	uncertain significance	7	152660772	152660772	Human	1	name
12902347	CV407105	single nucleotide variant	NM_005431.2(XRCC2):c.40C>T (p.Leu14Phe)	Hereditary cancer-predisposing syndrome [RCV002323835]\|not provided [RCV000486879]	uncertain significance	7	152660782	152660782	Human	1	name
13502814	CV474522	single nucleotide variant	NM_005431.2(XRCC2):c.825T>C (p.Ser275=)	Hereditary cancer-predisposing syndrome [RCV000575694]\|XRCC2-related disorder [RCV003935576]\|not provided [RCV000862334]	benign\|likely benign	7	152648660	152648660	Human	1	name , trait , alternate_id
13471925	CV474527	single nucleotide variant	NM_005431.2(XRCC2):c.501C>T (p.Asn167=)	Hereditary cancer-predisposing syndrome [RCV000563922]\|not provided [RCV000877091]	likely benign	7	152648984	152648984	Human	1	name
13502013	CV474531	single nucleotide variant	NM_005431.2(XRCC2):c.49C>T (p.Arg17Ter)	Hereditary cancer-predisposing syndrome [RCV000574813]\|not provided [RCV001043034]	pathogenic\|likely pathogenic\|uncertain significance	7	152660773	152660773	Human	1	name
13490245	CV474618	single nucleotide variant	NM_005431.2(XRCC2):c.462T>C (p.Phe154=)	Hereditary cancer-predisposing syndrome [RCV000569536]\|XRCC2-related disorder [RCV003915666]\|not provided [RCV001445685]	likely benign	7	152649023	152649023	Human	1	name , trait , alternate_id
13541405	CV501970	single nucleotide variant	NM_005431.2(XRCC2):c.327A>G (p.Lys109=)	Hereditary cancer-predisposing syndrome [RCV004024932]\|not specified [RCV000616116]	likely benign	7	152649158	152649158	Human	1	name
13541064	CV502016	single nucleotide variant	NM_005431.2(XRCC2):c.591T>C (p.Thr197=)	Hereditary cancer-predisposing syndrome [RCV002358695]\|not specified [RCV000615617]	likely benign	7	152648894	152648894	Human	1	name
13537250	CV502029	single nucleotide variant	NM_005431.2(XRCC2):c.549T>C (p.Leu183=)	not specified [RCV000610146]	likely benign	7	152648936	152648936	Human		name
13536982	CV502030	single nucleotide variant	NM_005431.2(XRCC2):c.432C>T (p.Cys144=)	Hereditary cancer-predisposing syndrome [RCV002331088]\|not provided [RCV000883258]\|not specified [RCV000609760]	likely benign	7	152649053	152649053	Human	1	name
13538003	CV502316	single nucleotide variant	NM_005431.2(XRCC2):c.492A>G (p.Glu164=)	Hereditary cancer-predisposing syndrome [RCV002333987]\|not specified [RCV000611203]	likely benign	7	152648993	152648993	Human	1	name
14726428	CV635956	single nucleotide variant	NM_005431.2(XRCC2):c.37G>C (p.Glu13Gln)	Hereditary cancer-predisposing syndrome [RCV001021184]\|not provided [RCV000815635]	likely benign\|uncertain significance	7	152676043	152676043	Human	1	name
15105225	CV687009	single nucleotide variant	NM_005431.2(XRCC2):c.828G>A (p.Gly276=)	Hereditary cancer-predisposing syndrome [RCV002427176]\|not provided [RCV000871048]\|not specified [RCV001817005]	likely benign\|uncertain significance	7	152648657	152648657	Human	1	name
15103270	CV687010	single nucleotide variant	NM_005431.2(XRCC2):c.390T>G (p.Leu130=)	Hereditary cancer-predisposing syndrome [RCV002352575]\|not provided [RCV000870635]	benign\|likely benign	7	152649095	152649095	Human	1	name
15141430	CV692188	single nucleotide variant	NM_005431.2(XRCC2):c.699A>G (p.Gln233=)	Hereditary cancer-predisposing syndrome [RCV002363314]\|not provided [RCV000877672]	likely benign	7	152648786	152648786	Human	1	name
15165525	CV736038	single nucleotide variant	NM_005431.2(XRCC2):c.451C>T (p.Leu151=)	Hereditary cancer-predisposing syndrome [RCV002336886]\|not provided [RCV000904241]	likely benign	7	152649034	152649034	Human	1	name
15160961	CV750530	single nucleotide variant	NM_005431.2(XRCC2):c.750C>T (p.Ser250=)	Hereditary cancer-predisposing syndrome [RCV002390931]\|not provided [RCV000925590]	likely benign	7	152648735	152648735	Human	1	name
15164154	CV750531	single nucleotide variant	NM_005431.2(XRCC2):c.504A>G (p.Leu168=)	not provided [RCV000926311]	likely benign	7	152648981	152648981	Human		name
15126822	CV766190	single nucleotide variant	NM_005431.2(XRCC2):c.516T>C (p.Thr172=)	Hereditary cancer-predisposing syndrome [RCV002336979]\|not provided [RCV000941447]	likely benign	7	152648969	152648969	Human	1	name
15183241	CV766191	single nucleotide variant	NM_005431.2(XRCC2):c.360C>T (p.Cys120=)	not provided [RCV000930547]	likely benign	7	152649125	152649125	Human		name
15144149	CV782825	single nucleotide variant	NM_005431.2(XRCC2):c.777T>C (p.Cys259=)	Hereditary cancer-predisposing syndrome [RCV001026806]\|not provided [RCV000983445]	likely benign	7	152648708	152648708	Human	1	name
21069678	CV796006	single nucleotide variant	NM_005431.2(XRCC2):c.58G>A (p.Gly20Ser)	not provided [RCV000998963]	uncertain significance	7	152660764	152660764	Human		name
25326826	CV808989	single nucleotide variant	NM_005431.2(XRCC2):c.789C>T (p.Asn263=)	Hereditary cancer-predisposing syndrome [RCV001026923]\|not provided [RCV001408527]	likely benign	7	152648696	152648696	Human	1	name
25326452	CV808990	single nucleotide variant	NM_005431.2(XRCC2):c.756A>G (p.Gln252=)	Hereditary cancer-predisposing syndrome [RCV001026574]	likely benign	7	152648729	152648729	Human	1	name
25326409	CV808992	single nucleotide variant	NM_005431.2(XRCC2):c.753C>T (p.Asn251=)	Hereditary cancer-predisposing syndrome [RCV001026539]	likely benign	7	152648732	152648732	Human	1	name
25323391	CV809004	single nucleotide variant	NM_005431.2(XRCC2):c.534G>A (p.Gln178=)	Hereditary cancer-predisposing syndrome [RCV001023962]\|not provided [RCV002550895]	likely benign	7	152648951	152648951	Human	1	name
25319343	CV809008	single nucleotide variant	NM_005431.2(XRCC2):c.435T>C (p.Leu145=)	Hereditary cancer-predisposing syndrome [RCV001022357]\|not provided [RCV002069018]	likely benign	7	152649050	152649050	Human	1	name
25317700	CV809010	single nucleotide variant	NM_005431.2(XRCC2):c.381T>G (p.Leu127=)	Hereditary cancer-predisposing syndrome [RCV001021227]	likely benign	7	152649104	152649104	Human	1	name
25316179	CV809015	single nucleotide variant	NM_005431.2(XRCC2):c.339A>C (p.Gly113=)	Hereditary cancer-predisposing syndrome [RCV001020192]\|not provided [RCV002549514]	likely benign	7	152649146	152649146	Human	1	name
25326946	CV809026	single nucleotide variant	NM_005431.2(XRCC2):c.79A>G (p.Ile27Val)	Hereditary cancer-predisposing syndrome [RCV001027032]\|not provided [RCV001326867]	uncertain significance	7	152660743	152660743	Human	1	name
25325201	CV809027	single nucleotide variant	NM_005431.2(XRCC2):c.65G>A (p.Ser22Asn)	Hereditary cancer-predisposing syndrome [RCV001025444]\|not provided [RCV003558644]	uncertain significance	7	152660757	152660757	Human	1	name
26902787	CV833380	single nucleotide variant	NM_005431.2(XRCC2):c.588A>G (p.Gln196=)	Hereditary cancer-predisposing syndrome [RCV004030717]\|not provided [RCV001069507]	likely benign\|uncertain significance	7	152648897	152648897	Human	1	name
26919484	CV833384	single nucleotide variant	NM_005431.2(XRCC2):c.46G>T (p.Ala16Ser)	Hereditary cancer-predisposing syndrome [RCV002339230]\|not provided [RCV001045634]	likely benign\|uncertain significance	7	152660776	152660776	Human	1	name
34889189	CV917953	single nucleotide variant	NM_005431.2(XRCC2):c.582G>T (p.Thr194=)	not provided [RCV001194886]	uncertain significance	7	152648903	152648903	Human		name
34889196	CV917957	duplication	NM_005431.2(XRCC2):c.247dup (p.Thr83fs)	not provided [RCV001194894]	uncertain significance	7	152649237	152649238	Human		name
38480989	CV924774	single nucleotide variant	NM_005431.2(XRCC2):c.59G>A (p.Gly20Asp)	Hereditary cancer-predisposing syndrome [RCV002356926]\|XRCC2-related disorder [RCV003398955]\|not provided [RCV001217794]	uncertain significance	7	152660763	152660763	Human	1	name , trait , alternate_id
38481904	CV933797	single nucleotide variant	NM_005431.2(XRCC2):c.40C>G (p.Leu14Val)	Hereditary cancer-predisposing syndrome [RCV002322014]\|not provided [RCV001207039]	uncertain significance	7	152660782	152660782	Human	1	name
38470998	CV933798	single nucleotide variant	NM_005431.2(XRCC2):c.29C>T (p.Ser10Phe)	Hereditary cancer-predisposing syndrome [RCV003353212]\|not provided [RCV001213679]	uncertain significance	7	152676051	152676051	Human	1	name
40907053	CV980132	single nucleotide variant	NM_005431.2(XRCC2):c.41T>C (p.Leu14Pro)	Hereditary cancer-predisposing syndrome [RCV002327617]\|Premature ovarian failure 17 [RCV001280535]\|Spermatogenic failure 50 [RCV001280534]\|not provided [RCV003738037]	pathogenic\|uncertain significance	7	152660781	152660781	Human	3	name
126741547	CV1007367	single nucleotide variant	NM_005431.2(XRCC2):c.281C>T (p.Thr94Ile)	Hereditary cancer-predisposing syndrome [RCV003166795]\|not provided [RCV001314536]	uncertain significance	7	152649204	152649204	Human	1	name
126740863	CV1027914	single nucleotide variant	NM_005431.2(XRCC2):c.181C>G (p.Leu61Val)	not provided [RCV001350802]	uncertain significance	7	152649304	152649304	Human		name
126918762	CV1044829	duplication	NM_005431.2(XRCC2):c.503dup (p.Leu168fs)	not provided [RCV001372849]	uncertain significance	7	152648981	152648982	Human		name
126919801	CV1044831	single nucleotide variant	NM_005431.2(XRCC2):c.126T>G (p.Asp42Glu)	Hereditary cancer-predisposing syndrome [RCV002377517]\|not provided [RCV001362504]	uncertain significance	7	152649359	152649359	Human	1	name
150548240	CV1310118	single nucleotide variant	NM_005431.2(XRCC2):c.213A>C (p.Glu71Asp)	not provided [RCV003238116]	uncertain significance	7	152649272	152649272	Human		name
151355380	CV1328447	single nucleotide variant	NM_005431.2(XRCC2):c.155C>A (p.Thr52Lys)	Hereditary cancer-predisposing syndrome [RCV002397762]\|not specified [RCV001820452]	uncertain significance	7	152649330	152649330	Human	1	name
8658380	CV133409	single nucleotide variant	NM_005431.2(XRCC2):c.140A>G (p.His47Arg)	Hereditary cancer-predisposing syndrome [RCV002390255]\|not provided [RCV001194892]\|not specified [RCV000115886]	uncertain significance	7	152649345	152649345	Human	1	name
8658381	CV133410	single nucleotide variant	NM_005431.2(XRCC2):c.268C>G (p.Leu90Val)	Hereditary cancer-predisposing syndrome [RCV002453427]\|not provided [RCV000115887]	uncertain significance	7	152649217	152649217	Human	1	name
8658382	CV133411	single nucleotide variant	NM_005431.2(XRCC2):c.283A>G (p.Ile95Val)	Fanconi anemia complementation group U [RCV000988018]\|Fanconi anemia complementation group U [RCV005031607]\|Hereditary cancer-predisposing syndrome [RCV000570999]\|XRCC2-related disorder [RCV003945051]\|not provided [RCV000791415]\|not specified [RCV000115888]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	7	152649202	152649202	Human	4	name , trait , alternate_id
8658386	CV133415	deletion	NM_005431.2(XRCC2):c.545del (p.Lys182fs)	Hereditary cancer-predisposing syndrome [RCV004678611]\|not specified [RCV000115892]	pathogenic\|likely pathogenic\|uncertain significance	7	152648940	152648940	Human	1	name
151767682	CV1341249	single nucleotide variant	NM_005431.2(XRCC2):c.193T>C (p.Cys65Arg)	Hereditary cancer-predisposing syndrome [RCV004681263]\|not provided [RCV001863772]	uncertain significance	7	152649292	152649292	Human	1	name
151795661	CV1415562	duplication	NM_005431.2(XRCC2):c.801dup (p.His268fs)	Hereditary cancer-predisposing syndrome [RCV004041530]\|not provided [RCV001898591]	uncertain significance	7	152648683	152648684	Human	1	name
151747785	CV1432532	single nucleotide variant	NM_005431.2(XRCC2):c.160A>G (p.Lys54Glu)	Hereditary cancer-predisposing syndrome [RCV003170344]\|not provided [RCV001985939]	uncertain significance	7	152649325	152649325	Human	1	name
151847678	CV1439713	single nucleotide variant	NM_005431.2(XRCC2):c.185C>T (p.Thr62Ile)	Hereditary cancer-predisposing syndrome [RCV002407291]\|not provided [RCV002016152]	uncertain significance	7	152649300	152649300	Human	1	name
151882568	CV1443244	deletion	NM_005431.2(XRCC2):c.603del (p.Ala202fs)	not provided [RCV002037165]	uncertain significance	7	152648882	152648882	Human		name
151737797	CV1463903	single nucleotide variant	NM_005431.2(XRCC2):c.120T>G (p.His40Gln)	Hereditary cancer-predisposing syndrome [RCV002359386]\|not provided [RCV001911616]	uncertain significance	7	152660702	152660702	Human	1	name
151829142	CV1491399	single nucleotide variant	NM_005431.2(XRCC2):c.245A>G (p.Asp82Gly)	not provided [RCV002030626]	uncertain significance	7	152649240	152649240	Human		name
153002339	CV1685337	single nucleotide variant	NM_005431.2(XRCC2):c.236T>C (p.Leu79Ser)	Hereditary cancer-predisposing syndrome [RCV002258711]	uncertain significance	7	152649249	152649249	Human	1	name
153002341	CV1685338	single nucleotide variant	NM_005431.2(XRCC2):c.238T>C (p.Phe80Leu)	Hereditary cancer-predisposing syndrome [RCV002258712]\|not provided [RCV003565508]	uncertain significance	7	152649247	152649247	Human	1	name
155691706	CV1794740	single nucleotide variant	NM_005431.2(XRCC2):c.112C>G (p.Pro38Ala)	Hereditary cancer-predisposing syndrome [RCV002320504]	uncertain significance	7	152660710	152660710	Human	1	name
155691880	CV1794768	single nucleotide variant	NM_005431.2(XRCC2):c.112C>T (p.Pro38Ser)	Hereditary cancer-predisposing syndrome [RCV002320532]	uncertain significance	7	152660710	152660710	Human	1	name
155734523	CV1797649	single nucleotide variant	NM_005431.2(XRCC2):c.116T>C (p.Val39Ala)	Hereditary cancer-predisposing syndrome [RCV002330054]\|not provided [RCV003094617]	uncertain significance	7	152660706	152660706	Human	1	name
155734025	CV1802193	duplication	NM_005431.2(XRCC2):c.488dup (p.Glu164fs)	Hereditary cancer-predisposing syndrome [RCV002340537]	likely pathogenic	7	152648996	152648997	Human	1	name
9834883	CV180247	single nucleotide variant	NM_005431.2(XRCC2):c.271C>T (p.Arg91Trp)	Fanconi anemia complementation group U [RCV001330061]\|Hereditary cancer-predisposing syndrome [RCV001016398]\|not provided [RCV000161106]	uncertain significance	7	152649214	152649214	Human	2	name
9834882	CV180248	single nucleotide variant	NM_005431.2(XRCC2):c.254A>C (p.Tyr85Ser)	Hereditary cancer-predisposing syndrome [RCV004019948]\|not provided [RCV000161105]	uncertain significance	7	152649231	152649231	Human	1	name
9834881	CV180249	single nucleotide variant	NM_005431.2(XRCC2):c.182T>C (p.Leu61Pro)	Hereditary cancer-predisposing syndrome [RCV001013342]\|not provided [RCV000161104]	uncertain significance	7	152649303	152649303	Human	1	name
9834880	CV180251	single nucleotide variant	NM_005431.2(XRCC2):c.115G>A (p.Val39Met)	Hereditary cancer-predisposing syndrome [RCV001010022]\|not provided [RCV000791369]\|not specified [RCV000161103]	conflicting interpretations of pathogenicity\|uncertain significance	7	152660707	152660707	Human	1	name
155705381	CV1811187	deletion	NM_005431.2(XRCC2):c.609del (p.Ser204fs)	Hereditary cancer-predisposing syndrome [RCV002360114]	likely pathogenic	7	152648876	152648876	Human	1	name
155693011	CV1818087	single nucleotide variant	NM_005431.2(XRCC2):c.127A>G (p.Ile43Val)	Hereditary cancer-predisposing syndrome [RCV002374328]	likely benign\|uncertain significance	7	152649358	152649358	Human	1	name
155730039	CV1819800	single nucleotide variant	NM_005431.2(XRCC2):c.124G>A (p.Asp42Asn)	Hereditary cancer-predisposing syndrome [RCV002400748]	uncertain significance	7	152649361	152649361	Human	1	name
155677902	CV1826257	single nucleotide variant	NM_005431.2(XRCC2):c.134A>C (p.Glu45Ala)	Hereditary cancer-predisposing syndrome [RCV002387903]	uncertain significance	7	152649351	152649351	Human	1	name
155718056	CV1827688	single nucleotide variant	NM_005431.2(XRCC2):c.158G>C (p.Gly53Ala)	Hereditary cancer-predisposing syndrome [RCV002398405]	uncertain significance	7	152649327	152649327	Human	1	name
155729565	CV1831523	single nucleotide variant	NM_005431.2(XRCC2):c.172C>A (p.Leu58Ile)	Hereditary cancer-predisposing syndrome [RCV002407403]\|not provided [RCV005097711]	uncertain significance	7	152649313	152649313	Human	1	name
155732715	CV1835434	single nucleotide variant	NM_005431.2(XRCC2):c.188C>T (p.Ala63Val)	Hereditary cancer-predisposing syndrome [RCV002407994]	uncertain significance	7	152649297	152649297	Human	1	name
155692620	CV1836933	single nucleotide variant	NM_005431.2(XRCC2):c.151G>A (p.Gly51Arg)	Hereditary cancer-predisposing syndrome [RCV002392396]	uncertain significance	7	152649334	152649334	Human	1	name
155702855	CV1838361	single nucleotide variant	NM_005431.2(XRCC2):c.105A>T (p.Glu35Asp)	Hereditary cancer-predisposing syndrome [RCV002401758]	uncertain significance	7	152660717	152660717	Human	1	name
155745762	CV1838818	single nucleotide variant	NM_005431.2(XRCC2):c.185C>A (p.Thr62Lys)	Hereditary cancer-predisposing syndrome [RCV002414888]	uncertain significance	7	152649300	152649300	Human	1	name
155705773	CV1841139	single nucleotide variant	NM_005431.2(XRCC2):c.227T>G (p.Val76Gly)	Hereditary cancer-predisposing syndrome [RCV002446073]	uncertain significance	7	152649258	152649258	Human	1	name
155692524	CV1841593	single nucleotide variant	NM_005431.2(XRCC2):c.239T>C (p.Phe80Ser)	Hereditary cancer-predisposing syndrome [RCV002459641]	uncertain significance	7	152649246	152649246	Human	1	name
155744199	CV1842987	single nucleotide variant	NM_005431.2(XRCC2):c.193T>G (p.Cys65Gly)	Hereditary cancer-predisposing syndrome [RCV002413169]	uncertain significance	7	152649292	152649292	Human	1	name
155712870	CV1845473	single nucleotide variant	NM_005431.2(XRCC2):c.248C>A (p.Thr83Lys)	Hereditary cancer-predisposing syndrome [RCV002430908]	uncertain significance	7	152649237	152649237	Human	1	name
155692793	CV1845787	deletion	NM_005431.2(XRCC2):c.26_27del (p.Glu9fs)	Hereditary cancer-predisposing syndrome [RCV002426242]	likely pathogenic\|uncertain significance	7	152676053	152676054	Human	1	name
155685269	CV1847836	single nucleotide variant	NM_005431.2(XRCC2):c.232G>T (p.Val78Phe)	Hereditary cancer-predisposing syndrome [RCV002457622]	uncertain significance	7	152649253	152649253	Human	1	name
155685392	CV1850167	single nucleotide variant	NM_005431.2(XRCC2):c.107A>T (p.Asp36Val)	Hereditary cancer-predisposing syndrome [RCV002424222]\|not provided [RCV003101055]	uncertain significance	7	152660715	152660715	Human	1	name
155700765	CV1851070	single nucleotide variant	NM_005431.2(XRCC2):c.230A>G (p.Glu77Gly)	Hereditary cancer-predisposing syndrome [RCV002428498]	uncertain significance	7	152649255	152649255	Human	1	name
155671872	CV1852286	single nucleotide variant	NM_005431.2(XRCC2):c.266T>C (p.Met89Thr)	Hereditary cancer-predisposing syndrome [RCV002437286]	uncertain significance	7	152649219	152649219	Human	1	name
155682435	CV1854705	single nucleotide variant	NM_005431.2(XRCC2):c.292C>T (p.His98Tyr)	Hereditary cancer-predisposing syndrome [RCV002440039]	uncertain significance	7	152649193	152649193	Human	1	name
156378178	CV2000553	single nucleotide variant	NM_005431.2(XRCC2):c.158G>A (p.Gly53Glu)	not provided [RCV002653459]	uncertain significance	7	152649327	152649327	Human		name
156110219	CV2008590	deletion	NM_005431.2(XRCC2):c.11_17del (p.Ala4fs)	not provided [RCV002695639]	uncertain significance	7	152676063	152676069	Human		name
156261310	CV2138651	single nucleotide variant	NM_005431.2(XRCC2):c.196A>G (p.Ile66Val)	not provided [RCV002988476]	uncertain significance	7	152649289	152649289	Human		name
11349306	CV240016	single nucleotide variant	NM_005431.2(XRCC2):c.242T>C (p.Ile81Thr)	not provided [RCV000230028]	uncertain significance	7	152649243	152649243	Human		name
329358465	CV2432331	single nucleotide variant	NM_005431.2(XRCC2):c.113C>T (p.Pro38Leu)	Hereditary cancer-predisposing syndrome [RCV003165248]	uncertain significance	7	152660709	152660709	Human	1	name
329384033	CV2432547	single nucleotide variant	NM_005431.2(XRCC2):c.293A>C (p.His98Pro)	Hereditary cancer-predisposing syndrome [RCV003176557]	uncertain significance	7	152649192	152649192	Human	1	name
329362762	CV2432548	deletion	NM_005431.2(XRCC2):c.801del (p.Lys267fs)	Hereditary cancer-predisposing syndrome [RCV003167963]	uncertain significance	7	152648684	152648684	Human	1	name
329362765	CV2432549	single nucleotide variant	NM_005431.2(XRCC2):c.259T>G (p.Phe87Val)	Hereditary cancer-predisposing syndrome [RCV003167964]	uncertain significance	7	152649226	152649226	Human	1	name
329384039	CV2432551	single nucleotide variant	NM_005431.2(XRCC2):c.176A>C (p.Tyr59Ser)	Hereditary cancer-predisposing syndrome [RCV003176559]	uncertain significance	7	152649309	152649309	Human	1	name
329362770	CV2432553	single nucleotide variant	NM_005431.2(XRCC2):c.191G>C (p.Arg64Pro)	Hereditary cancer-predisposing syndrome [RCV003167966]	uncertain significance	7	152649294	152649294	Human	1	name
11523298	CV244494	deletion	NM_005431.2(XRCC2):c.570del (p.Leu191fs)	not provided [RCV000235706]	uncertain significance	7	152648915	152648915	Human		name
11523308	CV244496	single nucleotide variant	NM_005431.2(XRCC2):c.232G>A (p.Val78Ile)	Hereditary cancer-predisposing syndrome [RCV002444937]\|not provided [RCV000235724]	uncertain significance	7	152649253	152649253	Human	1	name
11523844	CV244497	single nucleotide variant	NM_005431.2(XRCC2):c.181C>A (p.Leu61Ile)	Fanconi anemia complementation group U [RCV000765952]\|Hereditary cancer-predisposing syndrome [RCV001013301]\|not provided [RCV000657067]	likely benign\|uncertain significance	7	152649304	152649304	Human	2	name
401754897	CV2717572	single nucleotide variant	NM_005431.2(XRCC2):c.200T>C (p.Leu67Pro)	Hereditary cancer-predisposing syndrome [RCV003296723]	uncertain significance	7	152649285	152649285	Human	1	name
401899610	CV2790597	single nucleotide variant	NM_005431.2(XRCC2):c.198A>G (p.Ile66Met)	Hereditary cancer-predisposing syndrome [RCV003377781]	uncertain significance	7	152649287	152649287	Human	1	name
401962416	CV2843166	single nucleotide variant	NM_005431.2(XRCC2):c.290A>G (p.Glu97Gly)	not provided [RCV003477426]	uncertain significance	7	152649195	152649195	Human		name
402497486	CV2906062	deletion	NM_005431.2(XRCC2):c.304del (p.Gln102fs)	not provided [RCV003573649]	uncertain significance	7	152649181	152649181	Human		name
405032763	CV2922639	single nucleotide variant	NM_005431.2(XRCC2):c.217G>A (p.Gly73Ser)	not provided [RCV003578483]	uncertain significance	7	152649268	152649268	Human		name
405155600	CV3064818	single nucleotide variant	NM_005431.2(XRCC2):c.263A>G (p.Asp88Gly)	not provided [RCV003726724]	uncertain significance	7	152649222	152649222	Human		name
405152526	CV3138222	single nucleotide variant	NM_005431.2(XRCC2):c.130C>G (p.Leu44Val)	Hereditary cancer-predisposing syndrome [RCV004366903]\|not provided [RCV003840082]	uncertain significance	7	152649355	152649355	Human	1	name
405053199	CV3138354	single nucleotide variant	NM_005431.2(XRCC2):c.154A>G (p.Thr52Ala)	not provided [RCV003832198]	uncertain significance	7	152649331	152649331	Human		name
405703491	CV3387021	single nucleotide variant	NM_005431.2(XRCC2):c.100G>A (p.Asp34Asn)	Hereditary cancer-predisposing syndrome [RCV004521348]	uncertain significance	7	152660722	152660722	Human	1	name
405703503	CV3387022	single nucleotide variant	NM_005431.2(XRCC2):c.108T>G (p.Asp36Glu)	Hereditary cancer-predisposing syndrome [RCV004521349]	uncertain significance	7	152660714	152660714	Human	1	name
405703520	CV3387024	single nucleotide variant	NM_005431.2(XRCC2):c.128T>G (p.Ile43Ser)	Hereditary cancer-predisposing syndrome [RCV004521351]	uncertain significance	7	152649357	152649357	Human	1	name
405703533	CV3387026	single nucleotide variant	NM_005431.2(XRCC2):c.163A>G (p.Thr55Ala)	Hereditary cancer-predisposing syndrome [RCV004521353]	uncertain significance	7	152649322	152649322	Human	1	name
405703540	CV3387027	single nucleotide variant	NM_005431.2(XRCC2):c.172C>T (p.Leu58Phe)	Hereditary cancer-predisposing syndrome [RCV004521354]	uncertain significance	7	152649313	152649313	Human	1	name
405703548	CV3387028	single nucleotide variant	NM_005431.2(XRCC2):c.223G>A (p.Glu75Lys)	Hereditary cancer-predisposing syndrome [RCV004521355]	uncertain significance	7	152649262	152649262	Human	1	name
405703571	CV3387031	single nucleotide variant	NM_005431.2(XRCC2):c.247A>G (p.Thr83Ala)	Hereditary cancer-predisposing syndrome [RCV004521358]	uncertain significance	7	152649238	152649238	Human	1	name
405703579	CV3387032	single nucleotide variant	NM_005431.2(XRCC2):c.265A>G (p.Met89Val)	Hereditary cancer-predisposing syndrome [RCV004521359]	likely benign	7	152649220	152649220	Human	1	name
405703777	CV3387056	duplication	NM_005431.2(XRCC2):c.712dup (p.Arg238fs)	Hereditary cancer-predisposing syndrome [RCV004521383]	uncertain significance	7	152648772	152648773	Human	1	name
407456080	CV3493661	single nucleotide variant	NM_005431.2(XRCC2):c.150A>C (p.Glu50Asp)	Hereditary cancer-predisposing syndrome [RCV004685816]	uncertain significance	7	152649335	152649335	Human	1	name
407456108	CV3493674	single nucleotide variant	NM_005431.2(XRCC2):c.269T>C (p.Leu90Pro)	Hereditary cancer-predisposing syndrome [RCV004685826]	uncertain significance	7	152649216	152649216	Human	1	name
407456113	CV3493676	single nucleotide variant	NM_005431.2(XRCC2):c.267G>A (p.Met89Ile)	Hereditary cancer-predisposing syndrome [RCV004685828]	uncertain significance	7	152649218	152649218	Human	1	name
407508854	CV3496410	single nucleotide variant	NM_005431.2(XRCC2):c.286C>T (p.Leu96Phe)	not provided [RCV004698251]	uncertain significance	7	152649199	152649199	Human		name
596947270	CV3548820	deletion	NM_005431.2(XRCC2):c.626del (p.Pro209fs)	not provided [RCV004811144]	uncertain significance	7	152648859	152648859	Human		name
597677721	CV3630463	single nucleotide variant	NM_005431.2(XRCC2):c.104A>G (p.Glu35Gly)	Hereditary cancer-predisposing syndrome [RCV004950993]	uncertain significance	7	152660718	152660718	Human	1	name
597677844	CV3630480	single nucleotide variant	NM_005431.2(XRCC2):c.126T>A (p.Asp42Glu)	Hereditary cancer-predisposing syndrome [RCV004951006]	uncertain significance	7	152649359	152649359	Human	1	name
597677890	CV3630486	single nucleotide variant	NM_005431.2(XRCC2):c.155C>G (p.Thr52Arg)	Hereditary cancer-predisposing syndrome [RCV004951011]	uncertain significance	7	152649330	152649330	Human	1	name
597677983	CV3630497	deletion	NM_005431.2(XRCC2):c.723del (p.Ser242fs)	Hereditary cancer-predisposing syndrome [RCV004951021]	uncertain significance	7	152648762	152648762	Human	1	name
597847135	CV3768324	single nucleotide variant	NM_005431.2(XRCC2):c.233T>G (p.Val78Gly)	not provided [RCV005122703]	uncertain significance	7	152649252	152649252	Human		name
598241621	CV3933775	single nucleotide variant	NM_005431.2(XRCC2):c.119A>T (p.His40Leu)	Hereditary cancer-predisposing syndrome [RCV005296962]	uncertain significance	7	152660703	152660703	Human	1	name
598183271	CV3933780	single nucleotide variant	NM_005431.2(XRCC2):c.235T>G (p.Leu79Val)	Hereditary cancer-predisposing syndrome [RCV005311375]	uncertain significance	7	152649250	152649250	Human	1	name
598183276	CV3933782	single nucleotide variant	NM_005431.2(XRCC2):c.294C>G (p.His98Gln)	Hereditary cancer-predisposing syndrome [RCV005311376]	uncertain significance	7	152649191	152649191	Human	1	name
598195617	CV3933790	single nucleotide variant	NM_005431.2(XRCC2):c.230A>C (p.Glu77Ala)	Hereditary cancer-predisposing syndrome [RCV005313360]	uncertain significance	7	152649255	152649255	Human	1	name
598241675	CV3933791	single nucleotide variant	NM_005431.2(XRCC2):c.289G>A (p.Glu97Lys)	Hereditary cancer-predisposing syndrome [RCV005296972]	uncertain significance	7	152649196	152649196	Human	1	name
12900065	CV407079	duplication	NM_005431.2(XRCC2):c.810dup (p.Ile271fs)	Hereditary cancer-predisposing syndrome [RCV002257759]\|not provided [RCV000481579]	uncertain significance	7	152648674	152648675	Human	1	name
12898972	CV407080	deletion	NM_005431.2(XRCC2):c.803del (p.His268fs)	Hereditary cancer-predisposing syndrome [RCV001027098]\|not provided [RCV000479113]	uncertain significance	7	152648682	152648682	Human	1	name
12894088	CV407096	duplication	NM_005431.2(XRCC2):c.350dup (p.Leu117fs)	Fanconi anemia complementation group U [RCV001251190]\|Fanconi anemia complementation group U [RCV005044718]\|Hereditary cancer-predisposing syndrome [RCV002455921]\|not provided [RCV000481470]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	7	152649134	152649135	Human	2	name
12900699	CV407098	single nucleotide variant	NM_005431.2(XRCC2):c.262G>T (p.Asp88Tyr)	Hereditary cancer-predisposing syndrome [RCV001016093]\|not provided [RCV000482980]	uncertain significance	7	152649223	152649223	Human	1	name
12898799	CV407099	single nucleotide variant	NM_005431.2(XRCC2):c.199C>T (p.Leu67Phe)	Hereditary cancer-predisposing syndrome [RCV002420231]\|not provided [RCV000478713]	uncertain significance	7	152649286	152649286	Human	1	name
12901405	CV407101	single nucleotide variant	NM_005431.2(XRCC2):c.119A>G (p.His40Arg)	Hereditary cancer-predisposing syndrome [RCV002350055]\|XRCC2-related disorder [RCV003401518]\|not provided [RCV000484587]	uncertain significance	7	152660703	152660703	Human	1	name , trait , alternate_id
12899109	CV407102	single nucleotide variant	NM_005431.2(XRCC2):c.106G>A (p.Asp36Asn)	Hereditary cancer-predisposing syndrome [RCV001017195]\|not provided [RCV000479449]	uncertain significance	7	152660716	152660716	Human	1	name
13496785	CV474489	single nucleotide variant	NM_005431.2(XRCC2):c.190C>T (p.Arg64Ter)	Fanconi anemia complementation group U [RCV005034145]\|Hereditary cancer-predisposing syndrome [RCV000572575]\|not provided [RCV001312491]	pathogenic\|likely pathogenic\|uncertain significance	7	152649295	152649295	Human	2	name
13468002	CV474516	single nucleotide variant	NM_005431.2(XRCC2):c.272G>A (p.Arg91Gln)	Fanconi anemia complementation group U [RCV004760626]\|Hereditary cancer-predisposing syndrome [RCV000562172]\|not provided [RCV001349599]	uncertain significance	7	152649213	152649213	Human	2	name
13469663	CV474517	single nucleotide variant	NM_005431.2(XRCC2):c.223G>C (p.Glu75Gln)	Hereditary cancer-predisposing syndrome [RCV000562945]\|not provided [RCV001368535]\|not specified [RCV001194893]	likely benign\|uncertain significance	7	152649262	152649262	Human	1	name
13492002	CV474622	single nucleotide variant	NM_005431.2(XRCC2):c.178C>T (p.His60Tyr)	Hereditary cancer-predisposing syndrome [RCV000570344]	uncertain significance	7	152649307	152649307	Human	1	name
13820168	CV575542	single nucleotide variant	NM_005431.2(XRCC2):c.286C>A (p.Leu96Ile)	Hereditary cancer-predisposing syndrome [RCV000708765]	uncertain significance	7	152649199	152649199	Human	1	name
13820250	CV575760	single nucleotide variant	NM_005431.2(XRCC2):c.229G>C (p.Glu77Gln)	Fanconi anemia complementation group U [RCV000988019]\|Hereditary cancer-predisposing syndrome [RCV001015104]\|not provided [RCV001302553]	uncertain significance	7	152649256	152649256	Human	2	name
13836084	CV587353	single nucleotide variant	NM_005431.2(XRCC2):c.128T>A (p.Ile43Asn)	Hereditary cancer-predisposing syndrome [RCV002386303]\|not provided [RCV000732072]	uncertain significance	7	152649357	152649357	Human	1	name
14724791	CV635953	single nucleotide variant	NM_005431.2(XRCC2):c.248C>T (p.Thr83Ile)	Hereditary cancer-predisposing syndrome [RCV002427010]\|not provided [RCV000814929]	uncertain significance	7	152649237	152649237	Human	1	name
14711749	CV635954	single nucleotide variant	NM_005431.2(XRCC2):c.218G>C (p.Gly73Ala)	not provided [RCV000810058]	uncertain significance	7	152649267	152649267	Human		name
14726073	CV635955	single nucleotide variant	NM_005431.2(XRCC2):c.152G>A (p.Gly51Glu)	Hereditary cancer-predisposing syndrome [RCV002397693]\|not provided [RCV000815479]	uncertain significance	7	152649333	152649333	Human	1	name
25318251	CV677973	single nucleotide variant	NM_005431.2(XRCC2):c.268C>T (p.Leu90Phe)	Hereditary cancer-predisposing syndrome [RCV001005033]\|XRCC2-related disorder [RCV003411828]\|not provided [RCV003768620]	uncertain significance	7	152649217	152649217	Human	1	name , trait , alternate_id
25328779	CV809017	single nucleotide variant	NM_005431.2(XRCC2):c.272G>T (p.Arg91Leu)	Hereditary cancer-predisposing syndrome [RCV001016419]	uncertain significance	7	152649213	152649213	Human	1	name
25328451	CV809019	single nucleotide variant	NM_005431.2(XRCC2):c.250G>A (p.Asp84Asn)	Hereditary cancer-predisposing syndrome [RCV001015770]	uncertain significance	7	152649235	152649235	Human	1	name
25328045	CV809020	single nucleotide variant	NM_005431.2(XRCC2):c.226G>A (p.Val76Ile)	Hereditary cancer-predisposing syndrome [RCV001014999]\|not provided [RCV004998542]	likely benign\|uncertain significance	7	152649259	152649259	Human	1	name
25327438	CV809021	single nucleotide variant	NM_005431.2(XRCC2):c.206A>G (p.Lys69Arg)	Hereditary cancer-predisposing syndrome [RCV001014306]\|not provided [RCV001860759]	likely benign\|uncertain significance	7	152649279	152649279	Human	1	name
25326196	CV809022	single nucleotide variant	NM_005431.2(XRCC2):c.176A>G (p.Tyr59Cys)	Hereditary cancer-predisposing syndrome [RCV001013087]\|not provided [RCV001860735]	uncertain significance	7	152649309	152649309	Human	1	name
25324548	CV809023	single nucleotide variant	NM_005431.2(XRCC2):c.142G>A (p.Gly48Ser)	Hereditary cancer-predisposing syndrome [RCV001011542]	uncertain significance	7	152649343	152649343	Human	1	name
25323220	CV809024	single nucleotide variant	NM_005431.2(XRCC2):c.122G>A (p.Gly41Asp)	Hereditary cancer-predisposing syndrome [RCV001010449]\|not provided [RCV001860637]	uncertain significance	7	152649363	152649363	Human	1	name
26889739	CV833383	single nucleotide variant	NM_005431.2(XRCC2):c.122G>T (p.Gly41Val)	Hereditary cancer-predisposing syndrome [RCV002365723]\|not provided [RCV001058507]	uncertain significance	7	152649363	152649363	Human	1	name
34889197	CV917956	single nucleotide variant	NM_005431.2(XRCC2):c.283A>C (p.Ile95Leu)	not provided [RCV001194895]	uncertain significance	7	152649202	152649202	Human		name
34889198	CV917959	deletion	NM_005431.2(XRCC2):c.350del (p.Leu117fs)	Hereditary cancer-predisposing syndrome [RCV002451408]\|not provided [RCV001194896]	likely pathogenic\|uncertain significance	7	152649135	152649135	Human	1	name
38476651	CV924773	single nucleotide variant	NM_005431.2(XRCC2):c.119A>C (p.His40Pro)	Hereditary cancer-predisposing syndrome [RCV003163655]\|XRCC2-related disorder [RCV004731103]\|not provided [RCV001215750]	uncertain significance	7	152660703	152660703	Human	1	name , trait , alternate_id
38496082	CV945537	single nucleotide variant	NM_005431.2(XRCC2):c.280A>C (p.Thr94Pro)	not provided [RCV001226155]	uncertain significance	7	152649205	152649205	Human		name
38484937	CV945538	single nucleotide variant	NM_005431.2(XRCC2):c.143G>A (p.Gly48Asp)	not provided [RCV001236413]	uncertain significance	7	152649342	152649342	Human		name
38497449	CV955100	single nucleotide variant	NM_005431.2(XRCC2):c.191G>A (p.Arg64Gln)	Hereditary cancer-predisposing syndrome [RCV002411896]\|not provided [RCV001243176]	uncertain significance	7	152649294	152649294	Human	1	name
126759864	CV1007366	single nucleotide variant	NM_005431.2(XRCC2):c.794T>G (p.Leu265Ter)	not provided [RCV001318177]	uncertain significance	7	152648691	152648691	Human		name
126769757	CV1027911	single nucleotide variant	NM_005431.2(XRCC2):c.635C>T (p.Ala212Val)	Hereditary cancer-predisposing syndrome [RCV003169658]\|not provided [RCV001344098]	uncertain significance	7	152648850	152648850	Human	1	name
126750279	CV1027912	single nucleotide variant	NM_005431.2(XRCC2):c.361A>G (p.Ser121Gly)	Hereditary cancer-predisposing syndrome [RCV004679086]\|not provided [RCV001338013]	uncertain significance	7	152649124	152649124	Human	1	name
126774158	CV1027913	single nucleotide variant	NM_005431.2(XRCC2):c.325A>G (p.Lys109Glu)	Hereditary cancer-predisposing syndrome [RCV002322293]\|not provided [RCV001346900]	uncertain significance	7	152649160	152649160	Human	1	name
126922974	CV1044824	single nucleotide variant	NM_005431.2(XRCC2):c.653A>G (p.Asp218Gly)	Hereditary cancer-predisposing syndrome [RCV002368181]\|not provided [RCV001365314]	uncertain significance	7	152648832	152648832	Human	1	name
126923592	CV1044826	single nucleotide variant	NM_005431.2(XRCC2):c.619G>C (p.Glu207Gln)	Hereditary cancer-predisposing syndrome [RCV002368183]\|not provided [RCV001366020]	uncertain significance	7	152648866	152648866	Human	1	name
126924778	CV1044827	single nucleotide variant	NM_005431.2(XRCC2):c.614C>T (p.Ser205Leu)	not provided [RCV001367425]	uncertain significance	7	152648871	152648871	Human		name
126923844	CV1044828	single nucleotide variant	NM_005431.2(XRCC2):c.514A>C (p.Thr172Pro)	not provided [RCV001366318]	uncertain significance	7	152648971	152648971	Human		name
126924676	CV1044830	single nucleotide variant	NM_005431.2(XRCC2):c.403A>G (p.Ser135Gly)	not provided [RCV001367301]	uncertain significance	7	152649082	152649082	Human		name
150548239	CV1310117	single nucleotide variant	NM_005431.2(XRCC2):c.817G>A (p.Gly273Arg)	Hereditary cancer-predisposing syndrome [RCV004681250]\|not provided [RCV003238115]	uncertain significance	7	152648668	152648668	Human	1	name
8658383	CV133412	single nucleotide variant	NM_005431.2(XRCC2):c.450C>G (p.Ser150Arg)	Hereditary cancer-predisposing syndrome [RCV000574363]\|not provided [RCV000115889]	uncertain significance	7	152649035	152649035	Human	1	name
8658384	CV133413	single nucleotide variant	NM_005431.2(XRCC2):c.475C>T (p.Arg159Cys)	Hereditary cancer-predisposing syndrome [RCV001023001]\|not provided [RCV000115890]	uncertain significance	7	152649010	152649010	Human	1	name
8658385	CV133414	single nucleotide variant	NM_005431.2(XRCC2):c.476G>A (p.Arg159His)	Hereditary cancer-predisposing syndrome [RCV001023016]\|not provided [RCV001241826]\|not specified [RCV000115891]	uncertain significance	7	152649009	152649009	Human	1	name
8658387	CV133416	single nucleotide variant	NM_005431.2(XRCC2):c.580A>G (p.Thr194Ala)	Hereditary cancer-predisposing syndrome [RCV000572118]\|XRCC2-related disorder [RCV004748584]\|not provided [RCV000115893]	uncertain significance	7	152648905	152648905	Human	1	name , trait , alternate_id
8658388	CV133417	single nucleotide variant	NM_005431.2(XRCC2):c.620A>G (p.Glu207Gly)	Colon cancer [RCV000211556]\|Fanconi anemia complementation group U [RCV000988014]\|Hereditary cancer-predisposing syndrome [RCV000571792]\|not provided [RCV000791413]\|not specified [RCV000115894]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	7	152648865	152648865	Human	4	name
8658389	CV133418	single nucleotide variant	NM_005431.2(XRCC2):c.641G>A (p.Arg214Gln)	Colorectal cancer [RCV000417310]\|Hereditary cancer-predisposing syndrome [RCV001025247]\|not provided [RCV000115895]	likely benign\|uncertain significance	7	152648844	152648844	Human	3	name
8658390	CV133419	single nucleotide variant	NM_005431.2(XRCC2):c.667T>C (p.Tyr223His)	Fanconi anemia complementation group U [RCV005031608]\|Hereditary cancer-predisposing syndrome [RCV001025528]\|not provided [RCV000767012]	uncertain significance	7	152648818	152648818	Human	2	name
8658391	CV133420	single nucleotide variant	NM_005431.2(XRCC2):c.773G>A (p.Arg258His)	Fanconi anemia complementation group U [RCV005031609]\|Hereditary cancer-predisposing syndrome [RCV000567423]\|not provided [RCV000656992]	conflicting interpretations of pathogenicity\|uncertain significance	7	152648712	152648712	Human	2	name
8658392	CV133422	single nucleotide variant	NM_005431.2(XRCC2):c.808T>G (p.Phe270Val)	Fanconi anemia complementation group U [RCV000988009]\|Hereditary cancer-predisposing syndrome [RCV000565731]\|XRCC2-related disorder [RCV003925117]\|not provided [RCV000858406]\|not specified [RCV000115899]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	7	152648677	152648677	Human	2	name , trait , alternate_id
8658393	CV133423	single nucleotide variant	NM_005431.2(XRCC2):c.811A>G (p.Ile271Val)	Hereditary cancer-predisposing syndrome [RCV001027195]\|not provided [RCV000115900]	uncertain significance	7	152648674	152648674	Human	1	name
151832101	CV1356068	single nucleotide variant	NM_005431.2(XRCC2):c.789C>G (p.Asn263Lys)	not provided [RCV002030906]	uncertain significance	7	152648696	152648696	Human		name
151856381	CV1363603	single nucleotide variant	NM_005431.2(XRCC2):c.728A>G (p.Lys243Arg)	Hereditary cancer-predisposing syndrome [RCV003164113]\|not provided [RCV001904741]	uncertain significance	7	152648757	152648757	Human	1	name
151839256	CV1382868	single nucleotide variant	NM_005431.2(XRCC2):c.577G>C (p.Ala193Pro)	Hereditary cancer-predisposing syndrome [RCV002352772]\|not provided [RCV002031620]	uncertain significance	7	152648908	152648908	Human	1	name
151879600	CV1383718	single nucleotide variant	NM_005431.2(XRCC2):c.341G>A (p.Arg114Lys)	Hereditary cancer-predisposing syndrome [RCV002458673]\|not provided [RCV001907498]	uncertain significance	7	152649144	152649144	Human	1	name
151788662	CV1403362	single nucleotide variant	NM_005431.2(XRCC2):c.514A>G (p.Thr172Ala)	not provided [RCV001916598]	uncertain significance	7	152648971	152648971	Human		name
151753587	CV1407302	single nucleotide variant	NM_005431.2(XRCC2):c.710A>T (p.His237Leu)	Hereditary cancer-predisposing syndrome [RCV004947050]\|not provided [RCV002023639]	uncertain significance	7	152648775	152648775	Human	1	name
151747499	CV1432382	single nucleotide variant	NM_005431.2(XRCC2):c.578C>T (p.Ala193Val)	Hereditary cancer-predisposing syndrome [RCV002352695]\|not provided [RCV001985906]	uncertain significance	7	152648907	152648907	Human	1	name
151827583	CV1435411	single nucleotide variant	NM_005431.2(XRCC2):c.404G>A (p.Ser135Asn)	Hereditary cancer-predisposing syndrome [RCV002324365]\|not provided [RCV001955357]	uncertain significance	7	152649081	152649081	Human	1	name
151880881	CV1437197	single nucleotide variant	NM_005431.2(XRCC2):c.427C>G (p.Leu143Val)	not provided [RCV001999552]	uncertain significance	7	152649058	152649058	Human		name
151730099	CV1441091	single nucleotide variant	NM_005431.2(XRCC2):c.555T>G (p.Asn185Lys)	not provided [RCV001945950]	uncertain significance	7	152648930	152648930	Human		name
151774288	CV1455512	single nucleotide variant	NM_005431.2(XRCC2):c.605C>T (p.Ala202Val)	Hereditary cancer-predisposing syndrome [RCV002352745]\|not provided [RCV002045543]	uncertain significance	7	152648880	152648880	Human	1	name
151715220	CV1493041	single nucleotide variant	NM_005431.2(XRCC2):c.433C>T (p.Leu145Phe)	Hereditary cancer-predisposing syndrome [RCV005298908]\|not provided [RCV001890199]	uncertain significance	7	152649052	152649052	Human	1	name
151796717	CV1503740	single nucleotide variant	NM_005431.2(XRCC2):c.556G>T (p.Asp186Tyr)	not provided [RCV001973541]	uncertain significance	7	152648929	152648929	Human		name
153002532	CV1685339	single nucleotide variant	NM_005431.2(XRCC2):c.375C>G (p.His125Gln)	Hereditary cancer-predisposing syndrome [RCV002259280]	conflicting interpretations of pathogenicity\|uncertain significance	7	152649110	152649110	Human	1	name
153002342	CV1685340	single nucleotide variant	NM_005431.2(XRCC2):c.746G>C (p.Ser249Thr)	Hereditary cancer-predisposing syndrome [RCV002258713]	uncertain significance	7	152648739	152648739	Human	1	name
153002344	CV1685341	single nucleotide variant	NM_005431.2(XRCC2):c.795A>T (p.Leu265Phe)	Hereditary cancer-predisposing syndrome [RCV002258714]	uncertain significance	7	152648690	152648690	Human	1	name
155748792	CV1772349	single nucleotide variant	NM_005431.2(XRCC2):c.299T>C (p.Leu100Pro)	not provided [RCV002303923]	uncertain significance	7	152649186	152649186	Human		name
155744200	CV1777616	single nucleotide variant	NM_005431.2(XRCC2):c.343T>C (p.Phe115Leu)	not provided [RCV002303074]	uncertain significance	7	152649142	152649142	Human		name
155749017	CV1779069	single nucleotide variant	NM_005431.2(XRCC2):c.310T>C (p.Ser104Pro)	Hereditary cancer-predisposing syndrome [RCV004948696]\|not provided [RCV002304167]	uncertain significance	7	152649175	152649175	Human	1	name
155678765	CV1779287	single nucleotide variant	NM_005431.2(XRCC2):c.829G>T (p.Val277Phe)	Hereditary cancer-predisposing syndrome [RCV004681481]\|not provided [RCV002298034]	uncertain significance	7	152648656	152648656	Human	1	name
155729821	CV1786381	single nucleotide variant	NM_005431.2(XRCC2):c.355T>C (p.Tyr119His)	Hereditary cancer-predisposing syndrome [RCV002339780]	uncertain significance	7	152649130	152649130	Human	1	name
155693737	CV1787038	single nucleotide variant	NM_005431.2(XRCC2):c.388C>T (p.Leu130Phe)	Hereditary cancer-predisposing syndrome [RCV002357389]	uncertain significance	7	152649097	152649097	Human	1	name
155702063	CV1788391	single nucleotide variant	NM_005431.2(XRCC2):c.319A>G (p.Ile107Val)	Hereditary cancer-predisposing syndrome [RCV002322934]	uncertain significance	7	152649166	152649166	Human	1	name
155744616	CV1789536	single nucleotide variant	NM_005431.2(XRCC2):c.366T>G (p.Ser122Arg)	Hereditary cancer-predisposing syndrome [RCV002346668]	uncertain significance	7	152649119	152649119	Human	1	name
155664325	CV1790165	single nucleotide variant	NM_005431.2(XRCC2):c.386C>G (p.Thr129Arg)	Hereditary cancer-predisposing syndrome [RCV002366254]	uncertain significance	7	152649099	152649099	Human	1	name
155695280	CV1792630	single nucleotide variant	NM_005431.2(XRCC2):c.346T>C (p.Phe116Leu)	Hereditary cancer-predisposing syndrome [RCV002460253]	uncertain significance	7	152649139	152649139	Human	1	name
155685542	CV1793354	single nucleotide variant	NM_005431.2(XRCC2):c.379C>T (p.Leu127Phe)	Hereditary cancer-predisposing syndrome [RCV002355153]	uncertain significance	7	152649106	152649106	Human	1	name
155697330	CV1794046	single nucleotide variant	NM_005431.2(XRCC2):c.400G>A (p.Glu134Lys)	Hereditary cancer-predisposing syndrome [RCV002375710]	uncertain significance	7	152649085	152649085	Human	1	name
155692904	CV1794942	single nucleotide variant	NM_005431.2(XRCC2):c.313G>C (p.Glu105Gln)	Hereditary cancer-predisposing syndrome [RCV002320706]	uncertain significance	7	152649172	152649172	Human	1	name
155710635	CV1795065	single nucleotide variant	NM_005431.2(XRCC2):c.324C>G (p.Ile108Met)	Hereditary cancer-predisposing syndrome [RCV002324870]	uncertain significance	7	152649161	152649161	Human	1	name
155720707	CV1796637	single nucleotide variant	NM_005431.2(XRCC2):c.377T>G (p.Leu126Ter)	Hereditary cancer-predisposing syndrome [RCV002363888]\|not provided [RCV003476955]	likely pathogenic	7	152649108	152649108	Human	1	name
155672186	CV1798933	single nucleotide variant	NM_005431.2(XRCC2):c.490G>A (p.Glu164Lys)	Hereditary cancer-predisposing syndrome [RCV002351210]	uncertain significance	7	152648995	152648995	Human	1	name
155739706	CV1799147	single nucleotide variant	NM_005431.2(XRCC2):c.493A>T (p.Ser165Cys)	Hereditary cancer-predisposing syndrome [RCV002342670]	uncertain significance	7	152648992	152648992	Human	1	name
155667362	CV1799730	single nucleotide variant	NM_005431.2(XRCC2):c.541G>C (p.Glu181Gln)	Hereditary cancer-predisposing syndrome [RCV002349484]	uncertain significance	7	152648944	152648944	Human	1	name
155668673	CV1799944	single nucleotide variant	NM_005431.2(XRCC2):c.545A>C (p.Lys182Thr)	Hereditary cancer-predisposing syndrome [RCV002349698]	uncertain significance	7	152648940	152648940	Human	1	name
155669171	CV1800029	single nucleotide variant	NM_005431.2(XRCC2):c.546G>T (p.Lys182Asn)	Hereditary cancer-predisposing syndrome [RCV002349783]	uncertain significance	7	152648939	152648939	Human	1	name
155746442	CV1800165	single nucleotide variant	NM_005431.2(XRCC2):c.569T>A (p.Val190Asp)	Hereditary cancer-predisposing syndrome [RCV002347536]	uncertain significance	7	152648916	152648916	Human	1	name
155673170	CV1801260	single nucleotide variant	NM_005431.2(XRCC2):c.631C>G (p.His211Asp)	Hereditary cancer-predisposing syndrome [RCV002368855]	uncertain significance	7	152648854	152648854	Human	1	name
155683133	CV1801261	single nucleotide variant	NM_005431.2(XRCC2):c.631C>T (p.His211Tyr)	Hereditary cancer-predisposing syndrome [RCV002353989]\|not provided [RCV003660942]	uncertain significance	7	152648854	152648854	Human	1	name
9834888	CV180240	single nucleotide variant	NM_005431.2(XRCC2):c.826G>A (p.Gly276Arg)	Hereditary cancer-predisposing syndrome [RCV002426794]\|not provided [RCV000161111]	uncertain significance	7	152648659	152648659	Human	1	name
9834891	CV180242	single nucleotide variant	NM_005431.2(XRCC2):c.770C>T (p.Ser257Leu)	Hereditary cancer-predisposing syndrome [RCV001026743]\|not provided [RCV000161114]	uncertain significance	7	152648715	152648715	Human	1	name
9834887	CV180243	single nucleotide variant	NM_005431.2(XRCC2):c.678T>G (p.Tyr226Ter)	Hereditary cancer-predisposing syndrome [RCV002362852]\|not provided [RCV000161110]	uncertain significance	7	152648807	152648807	Human	1	name
9834886	CV180244	single nucleotide variant	NM_005431.2(XRCC2):c.613T>G (p.Ser205Ala)	Fanconi anemia complementation group U [RCV000988015]\|Hereditary cancer-predisposing syndrome [RCV001024935]\|not provided [RCV000726016]\|not specified [RCV000161109]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	7	152648872	152648872	Human	2	name
9834885	CV180245	single nucleotide variant	NM_005431.2(XRCC2):c.596T>C (p.Met199Thr)	Fanconi anemia complementation group U [RCV000765951]\|Hereditary cancer-predisposing syndrome [RCV001024734]\|not provided [RCV000767011]\|not specified [RCV001818361]	conflicting interpretations of pathogenicity\|uncertain significance	7	152648889	152648889	Human	2	name
9834884	CV180246	single nucleotide variant	NM_005431.2(XRCC2):c.562C>T (p.Arg188Cys)	Hereditary cancer-predisposing syndrome [RCV002257463]\|not provided [RCV000161107]	uncertain significance	7	152648923	152648923	Human	1	name
155741942	CV1802526	single nucleotide variant	NM_005431.2(XRCC2):c.511T>C (p.Ser171Pro)	Hereditary cancer-predisposing syndrome [RCV002344186]	uncertain significance	7	152648974	152648974	Human	1	name
155666831	CV1803095	single nucleotide variant	NM_005431.2(XRCC2):c.540A>T (p.Leu180Phe)	Hereditary cancer-predisposing syndrome [RCV002349396]	uncertain significance	7	152648945	152648945	Human	1	name
155665398	CV1804110	single nucleotide variant	NM_005431.2(XRCC2):c.621A>T (p.Glu207Asp)	Hereditary cancer-predisposing syndrome [RCV002366489]	uncertain significance	7	152648864	152648864	Human	1	name
155665964	CV1804224	single nucleotide variant	NM_005431.2(XRCC2):c.623A>G (p.Glu208Gly)	Hereditary cancer-predisposing syndrome [RCV002366602]	likely benign	7	152648862	152648862	Human	1	name
155666253	CV1804274	single nucleotide variant	NM_005431.2(XRCC2):c.624A>T (p.Glu208Asp)	Hereditary cancer-predisposing syndrome [RCV002366652]	uncertain significance	7	152648861	152648861	Human	1	name
155738406	CV1805140	single nucleotide variant	NM_005431.2(XRCC2):c.458C>G (p.Ala153Gly)	Hereditary cancer-predisposing syndrome [RCV002342264]	uncertain significance	7	152649027	152649027	Human	1	name
155711614	CV1805989	single nucleotide variant	NM_005431.2(XRCC2):c.506A>T (p.Gln169Leu)	Hereditary cancer-predisposing syndrome [RCV002335826]	uncertain significance	7	152648979	152648979	Human	1	name
155742563	CV1806102	single nucleotide variant	NM_005431.2(XRCC2):c.527G>T (p.Cys176Phe)	Hereditary cancer-predisposing syndrome [RCV002344444]	uncertain significance	7	152648958	152648958	Human	1	name
155676956	CV1806609	single nucleotide variant	NM_005431.2(XRCC2):c.556G>C (p.Asp186His)	Hereditary cancer-predisposing syndrome [RCV002352051]	uncertain significance	7	152648929	152648929	Human	1	name
155680428	CV1807214	single nucleotide variant	NM_005431.2(XRCC2):c.587A>C (p.Gln196Pro)	Hereditary cancer-predisposing syndrome [RCV002353503]	uncertain significance	7	152648898	152648898	Human	1	name
155705870	CV1807407	single nucleotide variant	NM_005431.2(XRCC2):c.611G>C (p.Ser204Thr)	Hereditary cancer-predisposing syndrome [RCV002360274]	uncertain significance	7	152648874	152648874	Human	1	name
155689820	CV1808135	single nucleotide variant	NM_005431.2(XRCC2):c.647T>C (p.Leu216Pro)	Hereditary cancer-predisposing syndrome [RCV002356203]	likely benign	7	152648838	152648838	Human	1	name
155730610	CV1808468	single nucleotide variant	NM_005431.2(XRCC2):c.450C>A (p.Ser150Arg)	Hereditary cancer-predisposing syndrome [RCV002339883]	uncertain significance	7	152649035	152649035	Human	1	name
155740477	CV1809416	single nucleotide variant	NM_005431.2(XRCC2):c.499A>T (p.Asn167Tyr)	Hereditary cancer-predisposing syndrome [RCV002342986]	uncertain significance	7	152648986	152648986	Human	1	name
155735148	CV1809819	single nucleotide variant	NM_005431.2(XRCC2):c.524A>C (p.Lys175Thr)	Hereditary cancer-predisposing syndrome [RCV002340930]	uncertain significance	7	152648961	152648961	Human	1	name
155669849	CV1810040	single nucleotide variant	NM_005431.2(XRCC2):c.548T>C (p.Leu183Pro)	Hereditary cancer-predisposing syndrome [RCV002349902]	uncertain significance	7	152648937	152648937	Human	1	name
155674893	CV1810211	single nucleotide variant	NM_005431.2(XRCC2):c.550G>A (p.Val184Ile)	Hereditary cancer-predisposing syndrome [RCV002351712]	uncertain significance	7	152648935	152648935	Human	1	name
155674820	CV1811494	single nucleotide variant	NM_005431.2(XRCC2):c.637T>C (p.Ser213Pro)	Hereditary cancer-predisposing syndrome [RCV002369120]	uncertain significance	7	152648848	152648848	Human	1	name
155674960	CV1811538	single nucleotide variant	NM_005431.2(XRCC2):c.638C>G (p.Ser213Cys)	Hereditary cancer-predisposing syndrome [RCV002369139]	uncertain significance	7	152648847	152648847	Human	1	name
155725913	CV1811806	single nucleotide variant	NM_005431.2(XRCC2):c.658G>A (p.Asp220Asn)	Hereditary cancer-predisposing syndrome [RCV002364531]	uncertain significance	7	152648827	152648827	Human	1	name
155726110	CV1811846	single nucleotide variant	NM_005431.2(XRCC2):c.659A>G (p.Asp220Gly)	Hereditary cancer-predisposing syndrome [RCV002364554]	uncertain significance	7	152648826	152648826	Human	1	name
155716056	CV1812462	single nucleotide variant	NM_005431.2(XRCC2):c.694C>T (p.Gln232Ter)	Hereditary cancer-predisposing syndrome [RCV002362450]	uncertain significance	7	152648791	152648791	Human	1	name
155747286	CV1813529	single nucleotide variant	NM_005431.2(XRCC2):c.791G>A (p.Ser264Asn)	Hereditary cancer-predisposing syndrome [RCV002416725]	likely benign	7	152648694	152648694	Human	1	name
155747404	CV1813632	single nucleotide variant	NM_005431.2(XRCC2):c.793T>A (p.Leu265Ile)	Hereditary cancer-predisposing syndrome [RCV002416828]	uncertain significance	7	152648692	152648692	Human	1	name
155729734	CV1814050	single nucleotide variant	NM_005431.2(XRCC2):c.832G>A (p.Glu278Lys)	Hereditary cancer-predisposing syndrome [RCV002434639]	uncertain significance	7	152648653	152648653	Human	1	name
155729935	CV1814073	single nucleotide variant	NM_005431.2(XRCC2):c.833A>G (p.Glu278Gly)	Hereditary cancer-predisposing syndrome [RCV002434658]	uncertain significance	7	152648652	152648652	Human	1	name
155731381	CV1814315	single nucleotide variant	NM_005431.2(XRCC2):c.839G>A (p.Cys280Tyr)	Hereditary cancer-predisposing syndrome [RCV002434882]	uncertain significance	7	152648646	152648646	Human	1	name
155714527	CV1815316	single nucleotide variant	NM_005431.2(XRCC2):c.685A>G (p.Lys229Glu)	Hereditary cancer-predisposing syndrome [RCV002362137]	uncertain significance	7	152648800	152648800	Human	1	name
155698348	CV1816892	single nucleotide variant	NM_005431.2(XRCC2):c.821A>C (p.Glu274Ala)	Hereditary cancer-predisposing syndrome [RCV002427977]	uncertain significance	7	152648664	152648664	Human	1	name
155698437	CV1816927	single nucleotide variant	NM_005431.2(XRCC2):c.822A>C (p.Glu274Asp)	Hereditary cancer-predisposing syndrome [RCV002427998]	uncertain significance	7	152648663	152648663	Human	1	name
155708133	CV1817195	single nucleotide variant	NM_005431.2(XRCC2):c.829G>A (p.Val277Ile)	Hereditary cancer-predisposing syndrome [RCV002430308]	uncertain significance	7	152648656	152648656	Human	1	name
155676340	CV1818668	single nucleotide variant	NM_005431.2(XRCC2):c.677A>T (p.Tyr226Phe)	Hereditary cancer-predisposing syndrome [RCV002369346]	uncertain significance	7	152648808	152648808	Human	1	name
155737539	CV1819966	single nucleotide variant	NM_005431.2(XRCC2):c.776G>A (p.Cys259Tyr)	Hereditary cancer-predisposing syndrome [RCV002409757]	uncertain significance	7	152648709	152648709	Human	1	name
155668603	CV1821945	single nucleotide variant	NM_005431.2(XRCC2):c.667T>G (p.Tyr223Asp)	Hereditary cancer-predisposing syndrome [RCV002367017]	uncertain significance	7	152648818	152648818	Human	1	name
155668801	CV1821978	single nucleotide variant	NM_005431.2(XRCC2):c.668A>G (p.Tyr223Cys)	Hereditary cancer-predisposing syndrome [RCV002367050]	uncertain significance	7	152648817	152648817	Human	1	name
155698503	CV1822176	single nucleotide variant	NM_005431.2(XRCC2):c.671G>C (p.Arg224Thr)	Hereditary cancer-predisposing syndrome [RCV002375923]	uncertain significance	7	152648814	152648814	Human	1	name
155675024	CV1822198	single nucleotide variant	NM_005431.2(XRCC2):c.672A>C (p.Arg224Ser)	Hereditary cancer-predisposing syndrome [RCV002369148]	uncertain significance	7	152648813	152648813	Human	1	name
155727624	CV1822645	single nucleotide variant	NM_005431.2(XRCC2):c.703G>T (p.Val235Leu)	Hereditary cancer-predisposing syndrome [RCV002364954]	uncertain significance	7	152648782	152648782	Human	1	name
155717393	CV1822958	single nucleotide variant	NM_005431.2(XRCC2):c.734A>T (p.Asp245Val)	Hereditary cancer-predisposing syndrome [RCV002380237]	uncertain significance	7	152648751	152648751	Human	1	name
155666560	CV1823669	single nucleotide variant	NM_005431.2(XRCC2):c.802C>T (p.His268Tyr)	Hereditary cancer-predisposing syndrome [RCV002419286]	uncertain significance	7	152648683	152648683	Human	1	name
155666873	CV1823748	single nucleotide variant	NM_005431.2(XRCC2):c.804T>A (p.His268Gln)	Hereditary cancer-predisposing syndrome [RCV002419328]\|not provided [RCV003574938]	uncertain significance	7	152648681	152648681	Human	1	name
155667402	CV1823855	single nucleotide variant	NM_005431.2(XRCC2):c.807T>G (p.Phe269Leu)	Hereditary cancer-predisposing syndrome [RCV002419402]	uncertain significance	7	152648678	152648678	Human	1	name
155668658	CV1856177	single nucleotide variant	NM_005431.2(XRCC2):c.301T>C (p.Ser101Pro)	Hereditary cancer-predisposing syndrome [RCV002435879]	uncertain significance	7	152649184	152649184	Human	1	name
156176844	CV2010407	single nucleotide variant	NM_005431.2(XRCC2):c.818G>A (p.Gly273Glu)	not provided [RCV002710657]	uncertain significance	7	152648667	152648667	Human		name
156207082	CV2021518	single nucleotide variant	NM_005431.2(XRCC2):c.501C>G (p.Asn167Lys)	Hereditary cancer-predisposing syndrome [RCV005301176]\|not provided [RCV002711616]	uncertain significance	7	152648984	152648984	Human	1	name
155933943	CV2060988	single nucleotide variant	NM_005431.2(XRCC2):c.674C>T (p.Pro225Leu)	not provided [RCV002815232]	uncertain significance	7	152648811	152648811	Human		name
156361695	CV2180432	single nucleotide variant	NM_005431.2(XRCC2):c.749G>C (p.Ser250Thr)	not provided [RCV003049067]	uncertain significance	7	152648736	152648736	Human		name
156109535	CV2254579	single nucleotide variant	NM_005431.2(XRCC2):c.671G>A (p.Arg224Lys)	Hereditary cancer-predisposing syndrome [RCV004123927]	uncertain significance	7	152648814	152648814	Human	1	name
11346102	CV240014	single nucleotide variant	NM_005431.2(XRCC2):c.714G>C (p.Arg238Ser)	Fanconi anemia complementation group U [RCV000988011]\|Hereditary cancer-predisposing syndrome [RCV000709047]\|not provided [RCV000657150]	uncertain significance	7	152648771	152648771	Human	2	name
11346751	CV240015	single nucleotide variant	NM_005431.2(XRCC2):c.608C>T (p.Ser203Leu)	Fanconi anemia complementation group U [RCV000988016]\|Hereditary cancer-predisposing syndrome [RCV001024881]\|not provided [RCV000229655]	uncertain significance	7	152648877	152648877	Human	2	name
329383608	CV2422414	single nucleotide variant	NM_005431.2(XRCC2):c.661A>G (p.Ile221Val)	Hereditary cancer-predisposing syndrome [RCV003176366]	likely benign	7	152648824	152648824	Human	1	name
329384275	CV2428755	single nucleotide variant	NM_005431.2(XRCC2):c.616T>G (p.Ser206Ala)	Hereditary cancer-predisposing syndrome [RCV003176643]\|not provided [RCV003575047]	likely benign\|uncertain significance	7	152648869	152648869	Human	1	name
329362990	CV2428828	single nucleotide variant	NM_005431.2(XRCC2):c.382C>A (p.Leu128Ile)	Hereditary cancer-predisposing syndrome [RCV003168074]	uncertain significance	7	152649103	152649103	Human	1	name
329383787	CV2432291	single nucleotide variant	NM_005431.2(XRCC2):c.506A>G (p.Gln169Arg)	Hereditary cancer-predisposing syndrome [RCV003176422]	uncertain significance	7	152648979	152648979	Human	1	name
329362759	CV2432546	single nucleotide variant	NM_005431.2(XRCC2):c.335T>C (p.Leu112Pro)	Hereditary cancer-predisposing syndrome [RCV003167962]	uncertain significance	7	152649150	152649150	Human	1	name
329384036	CV2432550	single nucleotide variant	NM_005431.2(XRCC2):c.759T>A (p.Phe253Leu)	Hereditary cancer-predisposing syndrome [RCV003176558]	uncertain significance	7	152648726	152648726	Human	1	name
329362768	CV2432552	single nucleotide variant	NM_005431.2(XRCC2):c.805T>C (p.Phe269Leu)	Hereditary cancer-predisposing syndrome [RCV003167965]	uncertain significance	7	152648680	152648680	Human	1	name
329362773	CV2432554	single nucleotide variant	NM_005431.2(XRCC2):c.467G>T (p.Trp156Leu)	Hereditary cancer-predisposing syndrome [RCV003167967]	uncertain significance	7	152649018	152649018	Human	1	name
11523949	CV244491	single nucleotide variant	NM_005431.2(XRCC2):c.650G>A (p.Cys217Tyr)	Hereditary cancer-predisposing syndrome [RCV002365230]\|not provided [RCV000236798]	uncertain significance	7	152648835	152648835	Human	1	name
11523265	CV244492	single nucleotide variant	NM_005431.2(XRCC2):c.644G>A (p.Arg215Gln)	Fanconi anemia complementation group U [RCV000988013]\|Hereditary cancer-predisposing syndrome [RCV000564280]\|not provided [RCV000235653]	likely benign\|uncertain significance	7	152648841	152648841	Human	2	name
11523888	CV244493	single nucleotide variant	NM_005431.2(XRCC2):c.596T>A (p.Met199Lys)	Hereditary cancer-predisposing syndrome [RCV004948234]\|not provided [RCV000236725]	uncertain significance	7	152648889	152648889	Human	1	name
11523089	CV244495	single nucleotide variant	NM_005431.2(XRCC2):c.353T>G (p.Val118Gly)	Hereditary cancer-predisposing syndrome [RCV002257606]\|XRCC2-related disorder [RCV003897576]\|not provided [RCV000235320]	uncertain significance	7	152649132	152649132	Human	1	name , trait , alternate_id
329367820	CV2457117	single nucleotide variant	NM_005431.2(XRCC2):c.508G>C (p.Glu170Gln)	Hereditary cancer-predisposing syndrome [RCV004264895]	uncertain significance	7	152648977	152648977	Human	1	name
401754881	CV2717566	single nucleotide variant	NM_005431.2(XRCC2):c.664G>T (p.Asp222Tyr)	Hereditary cancer-predisposing syndrome [RCV003296717]	uncertain significance	7	152648821	152648821	Human	1	name
401754884	CV2717567	single nucleotide variant	NM_005431.2(XRCC2):c.689C>T (p.Ala230Val)	Hereditary cancer-predisposing syndrome [RCV003296718]	uncertain significance	7	152648796	152648796	Human	1	name
401754886	CV2717568	single nucleotide variant	NM_005431.2(XRCC2):c.395C>A (p.Ser132Ter)	Hereditary cancer-predisposing syndrome [RCV003296719]	likely pathogenic	7	152649090	152649090	Human	1	name
401754890	CV2717569	single nucleotide variant	NM_005431.2(XRCC2):c.718T>G (p.Phe240Val)	Hereditary cancer-predisposing syndrome [RCV003296720]	uncertain significance	7	152648767	152648767	Human	1	name
401754893	CV2717570	single nucleotide variant	NM_005431.2(XRCC2):c.693G>C (p.Trp231Cys)	Hereditary cancer-predisposing syndrome [RCV003296721]	uncertain significance	7	152648792	152648792	Human	1	name
401754900	CV2717573	single nucleotide variant	NM_005431.2(XRCC2):c.691T>C (p.Trp231Arg)	Hereditary cancer-predisposing syndrome [RCV003296724]	uncertain significance	7	152648794	152648794	Human	1	name
401754902	CV2717574	single nucleotide variant	NM_005431.2(XRCC2):c.740C>G (p.Ser247Cys)	Hereditary cancer-predisposing syndrome [RCV003296725]	uncertain significance	7	152648745	152648745	Human	1	name
401783860	CV2720506	single nucleotide variant	NM_005431.2(XRCC2):c.727A>G (p.Lys243Glu)	Hereditary cancer-predisposing syndrome [RCV003310007]	uncertain significance	7	152648758	152648758	Human	1	name
401855179	CV2764044	single nucleotide variant	NM_005431.2(XRCC2):c.611G>A (p.Ser204Asn)	Hereditary cancer-predisposing syndrome [RCV003339268]	likely benign	7	152648874	152648874	Human	1	name
401869770	CV2764146	single nucleotide variant	NM_005431.2(XRCC2):c.827G>A (p.Gly276Glu)	Hereditary cancer-predisposing syndrome [RCV003361011]	uncertain significance	7	152648658	152648658	Human	1	name
401887740	CV2770400	single nucleotide variant	NM_005431.2(XRCC2):c.629C>T (p.Ser210Phe)	Hereditary cancer-predisposing syndrome [RCV003367314]	uncertain significance	7	152648856	152648856	Human	1	name
401875709	CV2789139	single nucleotide variant	NM_005431.2(XRCC2):c.801A>C (p.Lys267Asn)	Hereditary cancer-predisposing syndrome [RCV003383139]	uncertain significance	7	152648684	152648684	Human	1	name
401899609	CV2790596	single nucleotide variant	NM_005431.2(XRCC2):c.496G>A (p.Val166Met)	Hereditary cancer-predisposing syndrome [RCV003377780]	uncertain significance	7	152648989	152648989	Human	1	name
401899612	CV2790599	single nucleotide variant	NM_005431.2(XRCC2):c.739T>C (p.Ser247Pro)	Hereditary cancer-predisposing syndrome [RCV003377783]	uncertain significance	7	152648746	152648746	Human	1	name
401899614	CV2790601	single nucleotide variant	NM_005431.2(XRCC2):c.367A>T (p.Ser123Cys)	Hereditary cancer-predisposing syndrome [RCV003377785]	uncertain significance	7	152649118	152649118	Human	1	name
401899616	CV2790603	single nucleotide variant	NM_005431.2(XRCC2):c.701T>C (p.Leu234Pro)	Hereditary cancer-predisposing syndrome [RCV003377787]	uncertain significance	7	152648784	152648784	Human	1	name
401899617	CV2790604	single nucleotide variant	NM_005431.2(XRCC2):c.492A>C (p.Glu164Asp)	Hereditary cancer-predisposing syndrome [RCV003377788]	uncertain significance	7	152648993	152648993	Human	1	name
405216318	CV2872463	single nucleotide variant	NM_005431.2(XRCC2):c.559T>G (p.Tyr187Asp)	not provided [RCV003553243]	uncertain significance	7	152648926	152648926	Human		name
405147931	CV2881467	single nucleotide variant	NM_005431.2(XRCC2):c.470T>C (p.Ile157Thr)	Hereditary cancer-predisposing syndrome [RCV004369178]\|not provided [RCV003561381]	likely benign\|uncertain significance	7	152649015	152649015	Human	1	name
405222834	CV2891171	single nucleotide variant	NM_005431.2(XRCC2):c.794T>A (p.Leu265Ter)	not provided [RCV003554187]	uncertain significance	7	152648691	152648691	Human		name
405140476	CV2970307	single nucleotide variant	NM_005431.2(XRCC2):c.667T>A (p.Tyr223Asn)	not provided [RCV003669034]	uncertain significance	7	152648818	152648818	Human		name
405212592	CV3127523	single nucleotide variant	NM_005431.2(XRCC2):c.500A>G (p.Asn167Ser)	Hereditary cancer-predisposing syndrome [RCV004366783]\|not provided [RCV003823571]	uncertain significance	7	152648985	152648985	Human	1	name
405246784	CV3158589	single nucleotide variant	NM_005431.2(XRCC2):c.485G>T (p.Gly162Val)	not provided [RCV003868931]	uncertain significance	7	152649000	152649000	Human		name
405180731	CV3159442	single nucleotide variant	NM_005431.2(XRCC2):c.308G>C (p.Ser103Thr)	not provided [RCV003858692]	uncertain significance	7	152649177	152649177	Human		name
405666938	CV3349647	single nucleotide variant	NM_005431.2(XRCC2):c.350T>C (p.Leu117Ser)	Hereditary cancer-predisposing syndrome [RCV004485674]	uncertain significance	7	152649135	152649135	Human	1	name
405703585	CV3387033	single nucleotide variant	NM_005431.2(XRCC2):c.353T>A (p.Val118Glu)	Hereditary cancer-predisposing syndrome [RCV004521360]	uncertain significance	7	152649132	152649132	Human	1	name
405703599	CV3387035	single nucleotide variant	NM_005431.2(XRCC2):c.394T>C (p.Ser132Pro)	Hereditary cancer-predisposing syndrome [RCV004521362]	uncertain significance	7	152649091	152649091	Human	1	name
405703608	CV3387036	single nucleotide variant	NM_005431.2(XRCC2):c.408G>A (p.Met136Ile)	Hereditary cancer-predisposing syndrome [RCV004521363]	uncertain significance	7	152649077	152649077	Human	1	name
405703616	CV3387037	single nucleotide variant	NM_005431.2(XRCC2):c.415A>C (p.Ser139Arg)	Hereditary cancer-predisposing syndrome [RCV004521364]	uncertain significance	7	152649070	152649070	Human	1	name
405703627	CV3387038	single nucleotide variant	NM_005431.2(XRCC2):c.427C>T (p.Leu143Phe)	Hereditary cancer-predisposing syndrome [RCV004521365]	uncertain significance	7	152649058	152649058	Human	1	name
405703644	CV3387040	single nucleotide variant	NM_005431.2(XRCC2):c.457G>A (p.Ala153Thr)	Hereditary cancer-predisposing syndrome [RCV004521367]	uncertain significance	7	152649028	152649028	Human	1	name
405703655	CV3387041	single nucleotide variant	NM_005431.2(XRCC2):c.462T>G (p.Phe154Leu)	Hereditary cancer-predisposing syndrome [RCV004521368]	uncertain significance	7	152649023	152649023	Human	1	name
405703678	CV3387044	single nucleotide variant	NM_005431.2(XRCC2):c.488G>C (p.Gly163Ala)	Hereditary cancer-predisposing syndrome [RCV004521371]	uncertain significance	7	152648997	152648997	Human	1	name
405703686	CV3387045	single nucleotide variant	NM_005431.2(XRCC2):c.526T>C (p.Cys176Arg)	Hereditary cancer-predisposing syndrome [RCV004521372]	uncertain significance	7	152648959	152648959	Human	1	name
405703692	CV3387046	single nucleotide variant	NM_005431.2(XRCC2):c.539T>G (p.Leu180Ter)	Hereditary cancer-predisposing syndrome [RCV004521373]	likely pathogenic	7	152648946	152648946	Human	1	name
405703700	CV3387047	single nucleotide variant	NM_005431.2(XRCC2):c.589A>T (p.Thr197Ser)	Hereditary cancer-predisposing syndrome [RCV004521374]	likely benign	7	152648896	152648896	Human	1	name
405703711	CV3387048	single nucleotide variant	NM_005431.2(XRCC2):c.596T>G (p.Met199Arg)	Hereditary cancer-predisposing syndrome [RCV004521375]	uncertain significance	7	152648889	152648889	Human	1	name
405703718	CV3387049	single nucleotide variant	NM_005431.2(XRCC2):c.597G>A (p.Met199Ile)	Hereditary cancer-predisposing syndrome [RCV004521376]	uncertain significance	7	152648888	152648888	Human	1	name
405703726	CV3387050	single nucleotide variant	NM_005431.2(XRCC2):c.610A>T (p.Ser204Cys)	Hereditary cancer-predisposing syndrome [RCV004521377]	uncertain significance	7	152648875	152648875	Human	1	name
405703740	CV3387052	single nucleotide variant	NM_005431.2(XRCC2):c.632A>C (p.His211Pro)	Hereditary cancer-predisposing syndrome [RCV004521379]	likely benign	7	152648853	152648853	Human	1	name
405703758	CV3387054	single nucleotide variant	NM_005431.2(XRCC2):c.687G>C (p.Lys229Asn)	Hereditary cancer-predisposing syndrome [RCV004521381]	uncertain significance	7	152648798	152648798	Human	1	name
405703788	CV3387057	single nucleotide variant	NM_005431.2(XRCC2):c.717G>A (p.Met239Ile)	Hereditary cancer-predisposing syndrome [RCV004521384]	likely benign	7	152648768	152648768	Human	1	name
405703796	CV3387058	single nucleotide variant	NM_005431.2(XRCC2):c.721T>G (p.Phe241Val)	Hereditary cancer-predisposing syndrome [RCV004521385]	uncertain significance	7	152648764	152648764	Human	1	name
405703814	CV3387060	single nucleotide variant	NM_005431.2(XRCC2):c.743A>C (p.Gln248Pro)	Hereditary cancer-predisposing syndrome [RCV004521387]	likely benign	7	152648742	152648742	Human	1	name
405703822	CV3387061	single nucleotide variant	NM_005431.2(XRCC2):c.783A>C (p.Lys261Asn)	Hereditary cancer-predisposing syndrome [RCV004521388]	uncertain significance	7	152648702	152648702	Human	1	name
405703829	CV3387062	single nucleotide variant	NM_005431.2(XRCC2):c.784A>G (p.Ser262Gly)	Hereditary cancer-predisposing syndrome [RCV004521389]	uncertain significance	7	152648701	152648701	Human	1	name
405703839	CV3387063	single nucleotide variant	NM_005431.2(XRCC2):c.805T>A (p.Phe269Ile)	Hereditary cancer-predisposing syndrome [RCV004521390]	uncertain significance	7	152648680	152648680	Human	1	name
405703847	CV3387064	single nucleotide variant	NM_005431.2(XRCC2):c.809T>G (p.Phe270Cys)	Hereditary cancer-predisposing syndrome [RCV004521391]	uncertain significance	7	152648676	152648676	Human	1	name
407465672	CV3493664	single nucleotide variant	NM_005431.2(XRCC2):c.594A>G (p.Ile198Met)	Hereditary cancer-predisposing syndrome [RCV004688833]	uncertain significance	7	152648891	152648891	Human	1	name
407456094	CV3493669	single nucleotide variant	NM_005431.2(XRCC2):c.626C>T (p.Pro209Leu)	Hereditary cancer-predisposing syndrome [RCV004685821]	uncertain significance	7	152648859	152648859	Human	1	name
407456101	CV3493671	single nucleotide variant	NM_005431.2(XRCC2):c.679C>A (p.Leu227Ile)	Hereditary cancer-predisposing syndrome [RCV004685823]	uncertain significance	7	152648806	152648806	Human	1	name
407456103	CV3493672	single nucleotide variant	NM_005431.2(XRCC2):c.468G>T (p.Trp156Cys)	Hereditary cancer-predisposing syndrome [RCV004685824]	uncertain significance	7	152649017	152649017	Human	1	name
407456106	CV3493673	single nucleotide variant	NM_005431.2(XRCC2):c.493A>G (p.Ser165Gly)	Hereditary cancer-predisposing syndrome [RCV004685825]	uncertain significance	7	152648992	152648992	Human	1	name
407456111	CV3493675	single nucleotide variant	NM_005431.2(XRCC2):c.692G>T (p.Trp231Leu)	Hereditary cancer-predisposing syndrome [RCV004685827]	uncertain significance	7	152648793	152648793	Human	1	name
407456116	CV3493677	single nucleotide variant	NM_005431.2(XRCC2):c.466T>C (p.Trp156Arg)	Hereditary cancer-predisposing syndrome [RCV004685829]	uncertain significance	7	152649019	152649019	Human	1	name
407465680	CV3493681	single nucleotide variant	NM_005431.2(XRCC2):c.432C>G (p.Cys144Trp)	Hereditary cancer-predisposing syndrome [RCV004688835]	uncertain significance	7	152649053	152649053	Human	1	name
597677710	CV3630462	single nucleotide variant	NM_005431.2(XRCC2):c.613T>C (p.Ser205Pro)	Hereditary cancer-predisposing syndrome [RCV004950992]	uncertain significance	7	152648872	152648872	Human	1	name
597677778	CV3630472	single nucleotide variant	NM_005431.2(XRCC2):c.343T>A (p.Phe115Ile)	Hereditary cancer-predisposing syndrome [RCV004950999]	uncertain significance	7	152649142	152649142	Human	1	name
597677787	CV3630474	single nucleotide variant	NM_005431.2(XRCC2):c.416G>C (p.Ser139Thr)	Hereditary cancer-predisposing syndrome [RCV004951000]	uncertain significance	7	152649069	152649069	Human	1	name
597677797	CV3630475	single nucleotide variant	NM_005431.2(XRCC2):c.736G>T (p.Asp246Tyr)	Hereditary cancer-predisposing syndrome [RCV004951001]	uncertain significance	7	152648749	152648749	Human	1	name
597677806	CV3630476	single nucleotide variant	NM_005431.2(XRCC2):c.350T>G (p.Leu117Trp)	Hereditary cancer-predisposing syndrome [RCV004951002]	uncertain significance	7	152649135	152649135	Human	1	name
597677816	CV3630477	single nucleotide variant	NM_005431.2(XRCC2):c.797A>G (p.Lys266Arg)	Hereditary cancer-predisposing syndrome [RCV004951003]	uncertain significance	7	152648688	152648688	Human	1	name
597677824	CV3630478	single nucleotide variant	NM_005431.2(XRCC2):c.562C>A (p.Arg188Ser)	Hereditary cancer-predisposing syndrome [RCV004951004]	uncertain significance	7	152648923	152648923	Human	1	name
597677834	CV3630479	single nucleotide variant	NM_005431.2(XRCC2):c.488G>A (p.Gly163Glu)	Hereditary cancer-predisposing syndrome [RCV004951005]	uncertain significance	7	152648997	152648997	Human	1	name
597677859	CV3630482	single nucleotide variant	NM_005431.2(XRCC2):c.623A>C (p.Glu208Ala)	Hereditary cancer-predisposing syndrome [RCV004951008]	uncertain significance	7	152648862	152648862	Human	1	name
597677870	CV3630483	single nucleotide variant	NM_005431.2(XRCC2):c.735T>A (p.Asp245Glu)	Hereditary cancer-predisposing syndrome [RCV004951009]	uncertain significance	7	152648750	152648750	Human	1	name
597677881	CV3630485	single nucleotide variant	NM_005431.2(XRCC2):c.374A>T (p.His125Leu)	Hereditary cancer-predisposing syndrome [RCV004951010]	uncertain significance	7	152649111	152649111	Human	1	name
597677917	CV3630489	single nucleotide variant	NM_005431.2(XRCC2):c.746G>A (p.Ser249Asn)	Hereditary cancer-predisposing syndrome [RCV004951014]	uncertain significance	7	152648739	152648739	Human	1	name
597677927	CV3630490	single nucleotide variant	NM_005431.2(XRCC2):c.812T>C (p.Ile271Thr)	Hereditary cancer-predisposing syndrome [RCV004951015]	uncertain significance	7	152648673	152648673	Human	1	name
597677946	CV3630492	single nucleotide variant	NM_005431.2(XRCC2):c.421C>G (p.Pro141Ala)	Hereditary cancer-predisposing syndrome [RCV004951017]	uncertain significance	7	152649064	152649064	Human	1	name
597677956	CV3630494	single nucleotide variant	NM_005431.2(XRCC2):c.707A>G (p.Lys236Arg)	Hereditary cancer-predisposing syndrome [RCV004951018]	uncertain significance	7	152648778	152648778	Human	1	name
597677964	CV3630495	single nucleotide variant	NM_005431.2(XRCC2):c.428T>C (p.Leu143Pro)	Hereditary cancer-predisposing syndrome [RCV004951019]	uncertain significance	7	152649057	152649057	Human	1	name
597677993	CV3630498	single nucleotide variant	NM_005431.2(XRCC2):c.802C>A (p.His268Asn)	Hereditary cancer-predisposing syndrome [RCV004951022]	uncertain significance	7	152648683	152648683	Human	1	name
597678004	CV3630499	single nucleotide variant	NM_005431.2(XRCC2):c.796A>G (p.Lys266Glu)	Hereditary cancer-predisposing syndrome [RCV004951023]	uncertain significance	7	152648689	152648689	Human	1	name
597678012	CV3630500	single nucleotide variant	NM_005431.2(XRCC2):c.326A>G (p.Lys109Arg)	Hereditary cancer-predisposing syndrome [RCV004951024]	uncertain significance	7	152649159	152649159	Human	1	name
597702575	CV3718985	single nucleotide variant	NM_005431.2(XRCC2):c.563G>T (p.Arg188Leu)	Fanconi anemia complementation group U [RCV005033665]	uncertain significance	7	152648922	152648922	Human	1	name
597680166	CV3731146	duplication	NM_005431.2(XRCC2):c.64_65dup (p.Ser22fs)	not provided [RCV004998038]	uncertain significance	7	152660756	152660757	Human		name
597863142	CV3792407	single nucleotide variant	NM_005431.2(XRCC2):c.337G>C (p.Gly113Arg)	not provided [RCV005137294]	uncertain significance	7	152649148	152649148	Human		name
597863241	CV3800560	single nucleotide variant	NM_005431.2(XRCC2):c.371C>G (p.Thr124Ser)	not provided [RCV005137652]	uncertain significance	7	152649114	152649114	Human		name
597906146	CV3835431	single nucleotide variant	NM_005431.2(XRCC2):c.625C>T (p.Pro209Ser)	not provided [RCV005181154]	uncertain significance	7	152648860	152648860	Human		name
8602118	CV39018	single nucleotide variant	NM_005431.2(XRCC2):c.643C>T (p.Arg215Ter)	Fanconi anemia complementation group U [RCV000022966]\|Hereditary cancer-predisposing syndrome [RCV000210083]\|Short stature, microcephaly, and endocrine dysfunction [RCV001261591]\|not provided [RCV000236424]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	7	152648842	152648842	Human	3	name
598241631	CV3933777	single nucleotide variant	NM_005431.2(XRCC2):c.407T>C (p.Met136Thr)	Hereditary cancer-predisposing syndrome [RCV005296964]	uncertain significance	7	152649078	152649078	Human	1	name
598241637	CV3933778	single nucleotide variant	NM_005431.2(XRCC2):c.546G>C (p.Lys182Asn)	Hereditary cancer-predisposing syndrome [RCV005296965]	uncertain significance	7	152648939	152648939	Human	1	name
598241663	CV3933787	single nucleotide variant	NM_005431.2(XRCC2):c.748A>G (p.Ser250Gly)	Hereditary cancer-predisposing syndrome [RCV005296970]	uncertain significance	7	152648737	152648737	Human	1	name
598195613	CV3933788	single nucleotide variant	NM_005431.2(XRCC2):c.824G>T (p.Ser275Ile)	Hereditary cancer-predisposing syndrome [RCV005313359]	uncertain significance	7	152648661	152648661	Human	1	name
598195620	CV3933794	single nucleotide variant	NM_005431.2(XRCC2):c.412T>C (p.Cys138Arg)	Hereditary cancer-predisposing syndrome [RCV005313361]	uncertain significance	7	152649073	152649073	Human	1	name
598241692	CV3933795	single nucleotide variant	NM_005431.2(XRCC2):c.322A>G (p.Ile108Val)	Hereditary cancer-predisposing syndrome [RCV005296975]	uncertain significance	7	152649163	152649163	Human	1	name
598241698	CV3933796	single nucleotide variant	NM_005431.2(XRCC2):c.504A>C (p.Leu168Phe)	Hereditary cancer-predisposing syndrome [RCV005296976]	uncertain significance	7	152648981	152648981	Human	1	name
12897427	CV395534	single nucleotide variant	NM_005431.2(XRCC2):c.782A>C (p.Lys261Thr)	Hereditary cancer-predisposing syndrome [RCV002411485]\|not provided [RCV001308072]	uncertain significance	7	152648703	152648703	Human	1	name
12897979	CV395536	single nucleotide variant	NM_005431.2(XRCC2):c.413G>A (p.Cys138Tyr)	Hereditary cancer-predisposing syndrome [RCV002329065]\|not provided [RCV001317533]	uncertain significance	7	152649072	152649072	Human	1	name
12897444	CV395731	single nucleotide variant	NM_005431.2(XRCC2):c.515C>T (p.Thr172Ile)	Hereditary cancer-predisposing syndrome [RCV002339171]\|not provided [RCV001303880]	uncertain significance	7	152648970	152648970	Human	1	name
12897086	CV395736	single nucleotide variant	NM_005431.2(XRCC2):c.509A>C (p.Glu170Ala)	Hereditary cancer-predisposing syndrome [RCV000709057]\|not provided [RCV000457170]	uncertain significance	7	152648976	152648976	Human	1	name
12898334	CV395747	single nucleotide variant	NM_005431.2(XRCC2):c.433C>G (p.Leu145Val)	not provided [RCV000766306]	uncertain significance	7	152649052	152649052	Human		name
12898015	CV395896	single nucleotide variant	NM_005431.2(XRCC2):c.662T>C (p.Ile221Thr)	Fanconi anemia complementation group U [RCV005055112]\|Hereditary cancer-predisposing syndrome [RCV001025478]\|not provided [RCV000791389]\|not specified [RCV000470785]	likely benign\|uncertain significance	7	152648823	152648823	Human	2	name
12901162	CV407078	single nucleotide variant	NM_005431.2(XRCC2):c.821A>G (p.Glu274Gly)	Hereditary cancer-predisposing syndrome [RCV002431397]\|not provided [RCV000484060]	uncertain significance	7	152648664	152648664	Human	1	name
12898658	CV407082	single nucleotide variant	NM_005431.2(XRCC2):c.734A>G (p.Asp245Gly)	Hereditary cancer-predisposing syndrome [RCV001026307]\|not provided [RCV000478407]	uncertain significance	7	152648751	152648751	Human	1	name
12899182	CV407083	single nucleotide variant	NM_005431.2(XRCC2):c.730C>T (p.Gln244Ter)	Hereditary breast ovarian cancer syndrome [RCV001030743]\|Hereditary cancer-predisposing syndrome [RCV004023179]\|not provided [RCV000479614]	uncertain significance	7	152648755	152648755	Human	2	name
12899970	CV407084	single nucleotide variant	NM_005431.2(XRCC2):c.713G>A (p.Arg238Lys)	Hereditary cancer-predisposing syndrome [RCV003298550]\|not provided [RCV000481364]	uncertain significance	7	152648772	152648772	Human	1	name
12898632	CV407086	single nucleotide variant	NM_005431.2(XRCC2):c.544A>G (p.Lys182Glu)	not provided [RCV000478335]	uncertain significance	7	152648941	152648941	Human		name
12901507	CV407087	single nucleotide variant	NM_005431.2(XRCC2):c.539T>A (p.Leu180Ter)	not provided [RCV000484855]	uncertain significance	7	152648946	152648946	Human		name
12902426	CV407088	single nucleotide variant	NM_005431.2(XRCC2):c.527G>A (p.Cys176Tyr)	Hereditary cancer-predisposing syndrome [RCV001023852]\|not provided [RCV000487057]	uncertain significance	7	152648958	152648958	Human	1	name
12902046	CV407089	single nucleotide variant	NM_005431.2(XRCC2):c.482A>G (p.Asn161Ser)	Hereditary cancer-predisposing syndrome [RCV002341139]\|not provided [RCV000486150]	likely benign\|uncertain significance	7	152649003	152649003	Human	1	name
12899733	CV407090	single nucleotide variant	NM_005431.2(XRCC2):c.478G>A (p.Val160Ile)	Hereditary cancer-predisposing syndrome [RCV001023047]\|not provided [RCV000480843]	uncertain significance	7	152649007	152649007	Human	1	name
12901312	CV407091	single nucleotide variant	NM_005431.2(XRCC2):c.391T>C (p.Tyr131His)	Hereditary cancer-predisposing syndrome [RCV003168942]\|not provided [RCV000484380]	uncertain significance	7	152649094	152649094	Human	1	name
12899906	CV407092	single nucleotide variant	NM_005431.2(XRCC2):c.383T>C (p.Leu128Pro)	Hereditary cancer-predisposing syndrome [RCV001021268]\|not provided [RCV000481224]	uncertain significance	7	152649102	152649102	Human	1	name
12893895	CV407094	single nucleotide variant	NM_005431.2(XRCC2):c.377T>A (p.Leu126Ter)	Hereditary cancer-predisposing syndrome [RCV002346276]\|not provided [RCV002011163]	likely pathogenic\|uncertain significance	7	152649108	152649108	Human	1	name
12895470	CV407095	single nucleotide variant	NM_005431.2(XRCC2):c.367A>G (p.Ser123Gly)	Hereditary cancer-predisposing syndrome [RCV003352884]\|not provided [RCV000486576]	uncertain significance\|not provided	7	152649118	152649118	Human	1	name
12893536	CV407097	single nucleotide variant	NM_005431.2(XRCC2):c.340A>T (p.Arg114Ter)	not provided [RCV000479308]	likely pathogenic	7	152649145	152649145	Human		name
12905683	CV413763	single nucleotide variant	NM_005431.2(XRCC2):c.425C>T (p.Ser142Phe)	Hereditary cancer-predisposing syndrome [RCV003302722]\|not provided [RCV000487840]	uncertain significance	7	152649060	152649060	Human	1	name
13483448	CV474511	single nucleotide variant	NM_005431.2(XRCC2):c.659A>T (p.Asp220Val)	Fanconi anemia complementation group U [RCV002483544]\|Hereditary cancer-predisposing syndrome [RCV000567327]\|not provided [RCV001066340]	uncertain significance	7	152648826	152648826	Human	2	name
13491460	CV474617	single nucleotide variant	NM_005431.2(XRCC2):c.563G>A (p.Arg188His)	Fanconi anemia complementation group U [RCV003316748]\|Hereditary cancer-predisposing syndrome [RCV000570093]\|not provided [RCV001510671]	benign	7	152648922	152648922	Human	2	name
13509974	CV481784	single nucleotide variant	NM_005431.2(XRCC2):c.640C>T (p.Arg214Ter)	not provided [RCV000579199]	uncertain significance	7	152648845	152648845	Human		name
13540986	CV501688	single nucleotide variant	NM_005431.2(XRCC2):c.742C>G (p.Gln248Glu)	Hereditary cancer-predisposing syndrome [RCV001026424]\|not provided [RCV001194889]\|not specified [RCV000615501]	likely benign\|uncertain significance	7	152648743	152648743	Human	1	name
13705130	CV536325	deletion	NM_005431.2(XRCC2):c.96_99del (p.Phe32fs)	Hereditary cancer-predisposing syndrome [RCV002370382]\|not provided [RCV001904339]	pathogenic\|likely pathogenic\|uncertain significance	7	152660723	152660726	Human	1	name
13820243	CV575755	single nucleotide variant	NM_005431.2(XRCC2):c.794T>C (p.Leu265Ser)	Fanconi anemia complementation group U [RCV000988010]	uncertain significance	7	152648691	152648691	Human	1	name
13820244	CV575756	single nucleotide variant	NM_005431.2(XRCC2):c.698A>T (p.Gln233Leu)	Fanconi anemia complementation group U [RCV000988012]\|Hereditary cancer-predisposing syndrome [RCV000709048]\|not provided [RCV000817726]	uncertain significance	7	152648787	152648787	Human	2	name
13820246	CV575757	single nucleotide variant	NM_005431.2(XRCC2):c.679C>G (p.Leu227Val)	Hereditary cancer-predisposing syndrome [RCV000709049]\|not provided [RCV002532888]	uncertain significance	7	152648806	152648806	Human	1	name
13820247	CV575758	single nucleotide variant	NM_005431.2(XRCC2):c.581C>T (p.Thr194Met)	Fanconi anemia complementation group U [RCV005392320]\|Hereditary cancer-predisposing syndrome [RCV001024570]\|not provided [RCV001194885]	conflicting interpretations of pathogenicity\|uncertain significance	7	152648904	152648904	Human	2	name
13820248	CV575759	single nucleotide variant	NM_005431.2(XRCC2):c.574T>C (p.Phe192Leu)	Hereditary cancer-predisposing syndrome [RCV000709056]	uncertain significance	7	152648911	152648911	Human	1	name
14698706	CV624046	duplication	NM_005431.2(XRCC2):c.677dup (p.Tyr226Ter)	Hereditary breast ovarian cancer syndrome [RCV000787936]\|Hereditary cancer-predisposing syndrome [RCV003307419]	pathogenic\|uncertain significance	7	152648807	152648808	Human	2	name
14717058	CV635944	single nucleotide variant	NM_005431.2(XRCC2):c.753C>G (p.Asn251Lys)	Hereditary cancer-predisposing syndrome [RCV002390641]\|not provided [RCV000811759]	likely benign\|uncertain significance	7	152648732	152648732	Human	1	name
14706453	CV635945	single nucleotide variant	NM_005431.2(XRCC2):c.728A>C (p.Lys243Thr)	Hereditary cancer-predisposing syndrome [RCV002386374]\|not provided [RCV000792002]	uncertain significance	7	152648757	152648757	Human	1	name
14722932	CV635946	single nucleotide variant	NM_005431.2(XRCC2):c.586C>A (p.Gln196Lys)	not provided [RCV000797754]	uncertain significance	7	152648899	152648899	Human		name
14738535	CV635947	single nucleotide variant	NM_005431.2(XRCC2):c.406A>T (p.Met136Leu)	Hereditary cancer-predisposing syndrome [RCV005306158]\|not provided [RCV000804546]	uncertain significance	7	152649079	152649079	Human	1	name
14744167	CV635948	single nucleotide variant	NM_005431.2(XRCC2):c.386C>T (p.Thr129Ile)	Hereditary cancer-predisposing syndrome [RCV002363176]\|not provided [RCV000823908]	uncertain significance	7	152649099	152649099	Human	1	name
14728469	CV635949	single nucleotide variant	NM_005431.2(XRCC2):c.362G>A (p.Ser121Asn)	not provided [RCV000800069]	uncertain significance	7	152649123	152649123	Human		name
14719610	CV635950	single nucleotide variant	NM_005431.2(XRCC2):c.353T>C (p.Val118Ala)	Hereditary cancer-predisposing syndrome [RCV002336678]\|not provided [RCV000812670]	likely benign\|uncertain significance	7	152649132	152649132	Human	1	name
14718829	CV635951	single nucleotide variant	NM_005431.2(XRCC2):c.332G>T (p.Cys111Phe)	not provided [RCV000812356]	uncertain significance	7	152649153	152649153	Human		name
14729302	CV635952	single nucleotide variant	NM_005431.2(XRCC2):c.309C>G (p.Ser103Arg)	Hereditary cancer-predisposing syndrome [RCV005298614]\|not provided [RCV000800424]	uncertain significance	7	152649176	152649176	Human	1	name
21069677	CV796005	single nucleotide variant	NM_005431.2(XRCC2):c.561T>A (p.Tyr187Ter)	not provided [RCV000998962]	uncertain significance	7	152648924	152648924	Human		name
25327292	CV808987	single nucleotide variant	NM_005431.2(XRCC2):c.825T>G (p.Ser275Arg)	Fanconi anemia complementation group U [RCV005047216]\|Hereditary cancer-predisposing syndrome [RCV001027334]\|not provided [RCV001231344]	uncertain significance	7	152648660	152648660	Human	2	name
25326426	CV808991	single nucleotide variant	NM_005431.2(XRCC2):c.754C>G (p.Gln252Glu)	Hereditary cancer-predisposing syndrome [RCV001026550]\|not provided [RCV001226734]	uncertain significance	7	152648731	152648731	Human	1	name
25326264	CV808993	single nucleotide variant	NM_005431.2(XRCC2):c.740C>T (p.Ser247Phe)	Hereditary cancer-predisposing syndrome [RCV001026400]\|not provided [RCV001057024]	uncertain significance	7	152648745	152648745	Human	1	name
25326170	CV808994	single nucleotide variant	NM_005431.2(XRCC2):c.733G>T (p.Asp245Tyr)	Hereditary cancer-predisposing syndrome [RCV001026296]\|not provided [RCV001210522]	uncertain significance	7	152648752	152648752	Human	1	name
25326140	CV808995	single nucleotide variant	NM_005431.2(XRCC2):c.731A>G (p.Gln244Arg)	Hereditary cancer-predisposing syndrome [RCV001026268]\|not provided [RCV003558645]	uncertain significance	7	152648754	152648754	Human	1	name
25325784	CV808996	single nucleotide variant	NM_005431.2(XRCC2):c.703G>C (p.Val235Leu)	Hereditary cancer-predisposing syndrome [RCV001025962]	uncertain significance	7	152648782	152648782	Human	1	name
25325494	CV808997	single nucleotide variant	NM_005431.2(XRCC2):c.682T>C (p.Cys228Arg)	Hereditary cancer-predisposing syndrome [RCV001025701]\|not provided [RCV001862338]	uncertain significance	7	152648803	152648803	Human	1	name
25325160	CV808998	single nucleotide variant	NM_005431.2(XRCC2):c.655G>A (p.Val219Met)	Hereditary cancer-predisposing syndrome [RCV001025412]\|not provided [RCV001295981]	uncertain significance	7	152648830	152648830	Human	1	name
25324776	CV808999	single nucleotide variant	NM_005431.2(XRCC2):c.628T>C (p.Ser210Pro)	Hereditary cancer-predisposing syndrome [RCV001025092]	uncertain significance	7	152648857	152648857	Human	1	name
25324726	CV809000	single nucleotide variant	NM_005431.2(XRCC2):c.625C>A (p.Pro209Thr)	Hereditary cancer-predisposing syndrome [RCV001025052]\|not provided [RCV001341085]	likely benign\|uncertain significance	7	152648860	152648860	Human	1	name
25324518	CV809001	single nucleotide variant	NM_005431.2(XRCC2):c.607T>G (p.Ser203Ala)	Hereditary cancer-predisposing syndrome [RCV001024876]	uncertain significance	7	152648878	152648878	Human	1	name
25324301	CV809002	single nucleotide variant	NM_005431.2(XRCC2):c.592A>G (p.Ile198Val)	Hereditary cancer-predisposing syndrome [RCV001024692]\|not provided [RCV001060943]	uncertain significance	7	152648893	152648893	Human	1	name
25323951	CV809003	single nucleotide variant	NM_005431.2(XRCC2):c.565C>G (p.Leu189Val)	Hereditary cancer-predisposing syndrome [RCV001024377]	uncertain significance	7	152648920	152648920	Human	1	name
25322772	CV809005	single nucleotide variant	NM_005431.2(XRCC2):c.511T>A (p.Ser171Thr)	Hereditary cancer-predisposing syndrome [RCV001023576]\|not provided [RCV001321204]	likely benign\|uncertain significance	7	152648974	152648974	Human	1	name
25319600	CV809007	single nucleotide variant	NM_005431.2(XRCC2):c.440T>A (p.Ile147Asn)	Fanconi anemia complementation group U [RCV005036295]\|Hereditary cancer-predisposing syndrome [RCV001022442]\|not provided [RCV001361438]	uncertain significance	7	152649045	152649045	Human	2	name
25318485	CV809009	single nucleotide variant	NM_005431.2(XRCC2):c.413G>C (p.Cys138Ser)	Hereditary cancer-predisposing syndrome [RCV001021938]	uncertain significance	7	152649072	152649072	Human	1	name
25316736	CV809011	single nucleotide variant	NM_005431.2(XRCC2):c.359G>A (p.Cys120Tyr)	Hereditary cancer-predisposing syndrome [RCV001020683]\|not provided [RCV001194897]	uncertain significance	7	152649126	152649126	Human	1	name
25316724	CV809012	single nucleotide variant	NM_005431.2(XRCC2):c.358T>C (p.Cys120Arg)	Hereditary cancer-predisposing syndrome [RCV001020670]\|not provided [RCV001316460]	uncertain significance	7	152649127	152649127	Human	1	name
25316676	CV809013	single nucleotide variant	NM_005431.2(XRCC2):c.356A>C (p.Tyr119Ser)	Hereditary cancer-predisposing syndrome [RCV001020631]\|not provided [RCV001201801]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	7	152649129	152649129	Human	1	name
25316328	CV809014	single nucleotide variant	NM_005431.2(XRCC2):c.344T>G (p.Phe115Cys)	Hereditary cancer-predisposing syndrome [RCV001020334]	uncertain significance	7	152649141	152649141	Human	1	name
26917635	CV833379	single nucleotide variant	NM_005431.2(XRCC2):c.617C>T (p.Ser206Leu)	Hereditary cancer-predisposing syndrome [RCV004031275]\|not provided [RCV001042137]	uncertain significance	7	152648868	152648868	Human	1	name
26921723	CV833381	single nucleotide variant	NM_005431.2(XRCC2):c.571C>A (p.Leu191Ile)	not provided [RCV001050590]	uncertain significance	7	152648914	152648914	Human		name
26919472	CV833382	single nucleotide variant	NM_005431.2(XRCC2):c.501C>A (p.Asn167Lys)	Hereditary cancer-predisposing syndrome [RCV002258100]\|not provided [RCV001045603]	conflicting interpretations of pathogenicity\|uncertain significance	7	152648984	152648984	Human	1	name
34889194	CV917950	single nucleotide variant	NM_005431.2(XRCC2):c.772C>T (p.Arg258Cys)	Hereditary cancer-predisposing syndrome [RCV002402563]\|XRCC2-related disorder [RCV003908436]\|not provided [RCV001194890]	uncertain significance	7	152648713	152648713	Human	1	name , trait , alternate_id
34889191	CV917951	single nucleotide variant	NM_005431.2(XRCC2):c.693G>T (p.Trp231Cys)	not provided [RCV001194888]	uncertain significance	7	152648792	152648792	Human		name
34889190	CV917952	single nucleotide variant	NM_005431.2(XRCC2):c.595A>C (p.Met199Leu)	not provided [RCV001194887]	uncertain significance	7	152648890	152648890	Human		name
34889200	CV917954	single nucleotide variant	NM_005431.2(XRCC2):c.490G>C (p.Glu164Gln)	Hereditary cancer-predisposing syndrome [RCV002339492]\|not provided [RCV001194899]	uncertain significance	7	152648995	152648995	Human	1	name
34889199	CV917955	single nucleotide variant	NM_005431.2(XRCC2):c.398T>C (p.Leu133Pro)	not provided [RCV001194898]	uncertain significance	7	152649087	152649087	Human		name
38480477	CV924771	single nucleotide variant	NM_005431.2(XRCC2):c.563G>C (p.Arg188Pro)	Hereditary cancer-predisposing syndrome [RCV002348727]\|not provided [RCV001217558]	uncertain significance	7	152648922	152648922	Human	1	name
38482346	CV924772	single nucleotide variant	NM_005431.2(XRCC2):c.329A>G (p.Tyr110Cys)	Hereditary cancer-predisposing syndrome [RCV004679004]\|not provided [RCV001218422]	uncertain significance	7	152649156	152649156	Human	1	name
38488329	CV933796	single nucleotide variant	NM_005431.2(XRCC2):c.565C>A (p.Leu189Met)	Hereditary cancer-predisposing syndrome [RCV002348684]\|not provided [RCV001209698]	uncertain significance	7	152648920	152648920	Human	1	name
38488122	CV945536	single nucleotide variant	NM_005431.2(XRCC2):c.725C>T (p.Ser242Phe)	not provided [RCV001237886]	uncertain significance	7	152648760	152648760	Human		name
126766901	CV992211	single nucleotide variant	NM_005431.2(XRCC2):c.673C>T (p.Pro225Ser)	Hereditary cancer-predisposing syndrome [RCV002366136]\|not provided [RCV001302074]	uncertain significance	7	152648812	152648812	Human	1	name
126734220	CV992212	single nucleotide variant	NM_005431.2(XRCC2):c.619G>A (p.Glu207Lys)	not provided [RCV001304401]	uncertain significance	7	152648866	152648866	Human		name
126748629	CV992213	single nucleotide variant	NM_005431.2(XRCC2):c.598C>T (p.Gln200Ter)	not provided [RCV001306472]	uncertain significance	7	152648887	152648887	Human		name
126745577	CV992214	single nucleotide variant	NM_005431.2(XRCC2):c.560A>G (p.Tyr187Cys)	Hereditary cancer-predisposing syndrome [RCV002350521]\|not provided [RCV001296474]	uncertain significance	7	152648925	152648925	Human	1	name
11051404	CV226326	deletion	NM_005431.1(XRCC2):c.95delT (p.Phe32Leufs)	Hereditary cancer-predisposing syndrome [RCV000210130]	uncertain significance	7	152660727	152660727	Human		name
126754649	CV992215	deletion	NM_005431.2(XRCC2):c.63_65del (p.Arg21del)	not provided [RCV001307679]	uncertain significance	7	152660757	152660759	Human		name
155712227	CV1827971	deletion	NM_005431.2(XRCC2):c.166_167del (p.Glu56fs)	Hereditary cancer-predisposing syndrome [RCV002403816]	likely pathogenic	7	152649318	152649319	Human	1	name
155726438	CV1841625	microsatellite	NM_005431.2(XRCC2):c.240_243del (p.Phe80fs)	Hereditary cancer-predisposing syndrome [RCV002450253]	likely pathogenic	7	152649242	152649245	Human		name
150436709	CV1245980	deletion	NM_005431.2(XRCC2):c.347_350del (p.Phe116fs)	Breast carcinoma [RCV001663392]	likely pathogenic	7	152649135	152649138	Human	2	name
155686088	CV1793604	microsatellite	NM_005431.2(XRCC2):c.379CTT[1] (p.Leu128del)	Hereditary cancer-predisposing syndrome [RCV002355334]	uncertain significance	7	152649101	152649103	Human		name
155730024	CV1814091	deletion	NM_005431.2(XRCC2):c.834_843del (p.Glu278fs)	Hereditary cancer-predisposing syndrome [RCV002434674]\|not provided [RCV003718560]	uncertain significance	7	152648642	152648651	Human	1	name
155673749	CV1820304	microsatellite	NM_005431.2(XRCC2):c.811ATT[1] (p.Ile272del)	Hereditary cancer-predisposing syndrome [RCV002421373]	uncertain significance	7	152648669	152648671	Human		name
156357064	CV1901223	microsatellite	NM_005431.2(XRCC2):c.363TAG[1] (p.Ser123del)	Hereditary cancer-predisposing syndrome [RCV003161867]\|not provided [RCV002602241]	uncertain significance	7	152649117	152649119	Human		name
401933694	CV2799503	deletion	NM_005431.2(XRCC2):c.518_519del (p.Leu173fs)	XRCC2-related disorder [RCV003410560]	uncertain significance	7	152648966	152648967	Human		name , trait , alternate_id
597677850	CV3630481	deletion	NM_005431.2(XRCC2):c.653_657del (p.Asp218fs)	Hereditary cancer-predisposing syndrome [RCV004951007]	uncertain significance	7	152648828	152648832	Human	1	name
12897852	CV395526	deletion	NM_005431.2(XRCC2):c.789_790del (p.Asn263fs)	not provided [RCV001297351]	uncertain significance	7	152648695	152648696	Human		name
12894127	CV407093	microsatellite	NM_005431.2(XRCC2):c.378_381del (p.Leu126fs)	Fanconi anemia complementation group U [RCV000988017]\|Hereditary cancer-predisposing syndrome [RCV001021119]\|not provided [RCV000481611]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	7	152649104	152649107	Human		name
13705137	CV536324	microsatellite	NM_005431.2(XRCC2):c.820_821dup (p.Ser275fs)	Hereditary cancer-predisposing syndrome [RCV001027272]\|not provided [RCV000657408]	uncertain significance	7	152648663	152648664	Human		name
25322188	CV809006	microsatellite	NM_005431.2(XRCC2):c.490_491del (p.Glu164fs)	Hereditary cancer-predisposing syndrome [RCV001023237]	likely pathogenic	7	152648994	152648995	Human		name
26914033	CV833378	deletion	NM_005431.2(XRCC2):c.731_732del (p.Gln244fs)	Hereditary cancer-predisposing syndrome [RCV003307808]\|not provided [RCV001036931]	uncertain significance	7	152648753	152648754	Human	1	name
38491738	CV924770	microsatellite	NM_005431.2(XRCC2):c.619GAA[1] (p.Glu208del)	Hereditary cancer-predisposing syndrome [RCV003163734]\|not provided [RCV001223045]	uncertain significance	7	152648861	152648863	Human		name
9834893	CV180241	deletion	NM_005431.2(XRCC2):c.808_810del (p.Phe270del)	Hereditary cancer-predisposing syndrome [RCV001027150]\|not provided [RCV000161116]	uncertain significance	7	152648675	152648677	Human	1	name
155743868	CV1803208	indel	NM_005431.2(XRCC2):c.563_564delinsTT (p.Arg188Leu)	Hereditary cancer-predisposing syndrome [RCV002345084]	uncertain significance	7	152648921	152648922	Human		name
12901645	CV407081	indel	NM_005431.2(XRCC2):c.767_768delinsAG (p.Val256Glu)	not specified [RCV000485206]	uncertain significance	7	152648717	152648718	Human		name
151794931	CV1395142	deletion	NM_005431.2(XRCC2):c.455del (p.Leu151_Ser152insTer)	not provided [RCV001973390]	uncertain significance	7	152649030	152649030	Human		name
405239192	CV2886018	duplication	NM_005431.2(XRCC2):c.63_65dup (p.Arg21_Ser22insArg)	Hereditary cancer-predisposing syndrome [RCV004369208]\|not provided [RCV003557002]	uncertain significance	7	152660756	152660757	Human	1	name
38484998	CV924769	deletion	NM_005431.2(XRCC2):c.794del (p.Ser264_Leu265insTer)	not provided [RCV001219678]	uncertain significance	7	152648691	152648691	Human		name
12899523	CV407107	insertion	NM_005431.2(XRCC2):c.16_17insGAA (p.His6delinsArgAsn)	not provided [RCV000480402]	uncertain significance	7	152676063	152676064	Human		name
155717308	CV1822932	duplication	NM_005431.2(XRCC2):c.734_746dup (p.Ser249delinsArgTer)	Hereditary cancer-predisposing syndrome [RCV002380211]	uncertain significance	7	152648738	152648739	Human	1	name
597677759	CV3630470	deletion	NM_005431.2(XRCC2):c.316_319del (p.Glu105_Glu106insTer)	Hereditary cancer-predisposing syndrome [RCV004950997]	pathogenic	7	152649166	152649169	Human	1	name
243063693	CV2405171	deletion	NM_005431.2(XRCC2):c.756_758del (p.Gln252_Phe253delinsHis)	Fanconi anemia complementation group U [RCV003142303]	uncertain significance	7	152648727	152648729	Human	1	name
12899948	CV407085	microsatellite	NM_005431.2(XRCC2):c.651_652del (p.Cys217_Asp218delinsTer)	Fanconi anemia complementation group U [RCV005034015]\|Hereditary cancer-predisposing syndrome [RCV001025359]\|not provided [RCV000481321]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	7	152648833	152648834	Human		name
25326979	CV808988	deletion	NM_005431.2(XRCC2):c.801_803del (p.Lys267_His268delinsAsn)	Hereditary cancer-predisposing syndrome [RCV001027061]	uncertain significance	7	152648682	152648684	Human	1	name
155743870	CV1803209	indel	NM_005431.2(XRCC2):c.563_565delinsACA (p.Arg188_Leu189delinsHisMet)	Hereditary cancer-predisposing syndrome [RCV002345085]	uncertain significance	7	152648920	152648922	Human		name
8658842	CV133421	indel	NM_005431.2(XRCC2):c.776_786delinsTAAAC (p.Cys259_Ser262delinsLeuAsn)	not specified [RCV000115898]	uncertain significance	7	152648699	152648709	Human		name
151738604	CV1469579	insertion	NM_005431.2(XRCC2):c.822_823insTTTTTTTTTTTTTTTTTNNNNNNNNNNNNGATCTCCTGACCTCATGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCAGCC (p.Ser275delinsPhePhePhePhePheXaaXaaXaaXaaXaaIleSerTer)	not provided [RCV002041999]	uncertain significance	7	152648662	152648663	Human		name

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