Cd81 Variant Search Result - Rat Genome Database

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270 records found for search term Cd81

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405289728	CV3221106	single nucleotide variant	NM_004356.4(CD81):c.*7G>A	CD81-related disorder [RCV003961901]	likely benign	11	2396873	2396873	Human		name , trait , alternate_id
14396735	CV612907	single nucleotide variant	NM_004356.4(CD81):c.-3G>A	not provided [RCV000761756]	uncertain significance	11	2377547	2377547	Human		name
150485918	CV1223099	single nucleotide variant	NM_004356.4(CD81):c.*241A>G	not provided [RCV001617812]	benign	11	2397107	2397107	Human		name
150464883	CV1277146	duplication	NM_004356.4(CD81):c.*256dup	not provided [RCV001710440]	benign	11	2397119	2397120	Human		name
156150732	CV2070257	single nucleotide variant	NM_004356.4(CD81):c.66+4A>G	not provided [RCV002850861]	uncertain significance	11	2377619	2377619	Human		name
405067180	CV2936629	single nucleotide variant	NM_004356.4(CD81):c.67-9C>T	not provided [RCV003659127]	likely benign	11	2390403	2390403	Human		name
127290557	CV1156676	single nucleotide variant	NM_004356.4(CD81):c.67-15C>T	not provided [RCV001509881]	benign	11	2390397	2390397	Human		name
151726314	CV1352836	single nucleotide variant	NM_004356.4(CD81):c.561+5G>C	not provided [RCV001891764]	uncertain significance	11	2395975	2395975	Human		name
151735837	CV1354770	single nucleotide variant	NM_004356.4(CD81):c.561+6C>T	not provided [RCV001892747]	uncertain significance	11	2395976	2395976	Human		name
151749850	CV1358973	single nucleotide variant	NM_004356.4(CD81):c.67-19T>A	not provided [RCV001969078]	likely benign\|uncertain significance	11	2390393	2390393	Human		name
151768115	CV1387876	single nucleotide variant	NM_004356.4(CD81):c.355-6C>G	not provided [RCV001970914]	likely benign\|uncertain significance	11	2395410	2395410	Human		name
151743784	CV1431797	single nucleotide variant	NM_004356.4(CD81):c.648+6C>T	not provided [RCV001926735]	uncertain significance	11	2396720	2396720	Human		name
151756208	CV1498985	single nucleotide variant	NM_004356.4(CD81):c.280-9C>T	not provided [RCV002023870]	likely benign	11	2394963	2394963	Human		name
152057167	CV1588409	single nucleotide variant	NM_004356.4(CD81):c.182-6C>T	not provided [RCV002190104]	likely benign	11	2394089	2394089	Human		name
152085584	CV1608209	single nucleotide variant	NM_004356.4(CD81):c.66+11C>G	not provided [RCV002211998]	likely benign	11	2377626	2377626	Human		name
152134075	CV1613294	single nucleotide variant	NM_004356.4(CD81):c.67-13C>T	not provided [RCV002155916]	benign	11	2390399	2390399	Human		name
152160567	CV1650168	single nucleotide variant	NM_004356.4(CD81):c.67-20C>A	not provided [RCV002159561]	likely benign	11	2390392	2390392	Human		name
156163694	CV1971356	deletion	NM_004356.4(CD81):c.66+19del	not provided [RCV002594554]	benign	11	2377630	2377630	Human		name
156134936	CV1977218	single nucleotide variant	NM_004356.4(CD81):c.561+6C>G	not provided [RCV002593629]	uncertain significance	11	2395976	2395976	Human		name
155953441	CV2033248	single nucleotide variant	NM_004356.4(CD81):c.561+5G>A	not provided [RCV002730802]	uncertain significance	11	2395975	2395975	Human		name
155915480	CV2033409	single nucleotide variant	NM_004356.4(CD81):c.279+8A>G	not provided [RCV002750442]	likely benign	11	2394200	2394200	Human		name
156235465	CV2056259	single nucleotide variant	NM_004356.4(CD81):c.561+7G>T	not provided [RCV002791155]	likely benign	11	2395977	2395977	Human		name
156221557	CV2067915	single nucleotide variant	NM_004356.4(CD81):c.562-7C>G	not provided [RCV002829704]	uncertain significance	11	2396621	2396621	Human		name
8563293	CV27782	single nucleotide variant	NM_004356.4(CD81):c.561+1G>A	Immunodeficiency, common variable, 6 [RCV000013580]	pathogenic	11	2395971	2395971	Human	1	name , alternate_id
405134814	CV2957962	single nucleotide variant	NM_004356.4(CD81):c.459+4C>G	not provided [RCV003672721]	uncertain significance	11	2395524	2395524	Human		name
404979272	CV3009529	single nucleotide variant	NM_004356.4(CD81):c.561+8A>T	not provided [RCV003690956]	likely benign	11	2395978	2395978	Human		name
405117053	CV3115811	single nucleotide variant	NM_004356.4(CD81):c.561+4C>T	not provided [RCV003814301]	uncertain significance	11	2395974	2395974	Human		name
405120150	CV3131450	single nucleotide variant	NM_004356.4(CD81):c.561+7G>C	not provided [RCV003837314]	likely benign	11	2395977	2395977	Human		name
404994527	CV3132586	single nucleotide variant	NM_004356.4(CD81):c.182-4C>T	not provided [RCV003827525]	likely benign	11	2394091	2394091	Human		name
405079300	CV3137092	single nucleotide variant	NM_004356.4(CD81):c.460-8C>G	not provided [RCV003833991]	likely benign	11	2395861	2395861	Human		name
405214788	CV3143089	single nucleotide variant	NM_004356.4(CD81):c.649-6C>T	not provided [RCV003846252]	likely benign	11	2396798	2396798	Human		name
402509807	CV3182203	single nucleotide variant	NM_004356.4(CD81):c.280-4C>T	not provided [RCV003878857]	likely benign	11	2394968	2394968	Human		name
597942189	CV3779851	single nucleotide variant	NM_004356.4(CD81):c.182-6C>G	not provided [RCV005118860]	likely benign	11	2394089	2394089	Human		name
597921487	CV3808051	single nucleotide variant	NM_004356.4(CD81):c.648+5G>A	not provided [RCV005155759]	uncertain significance	11	2396719	2396719	Human		name
597878339	CV3813673	single nucleotide variant	NM_004356.4(CD81):c.67-12G>A	not provided [RCV005149415]	likely benign	11	2390400	2390400	Human		name
597864517	CV3814232	single nucleotide variant	NM_004356.4(CD81):c.459+5G>A	not provided [RCV005147301]	uncertain significance	11	2395525	2395525	Human		name
597949337	CV3818541	single nucleotide variant	NM_004356.4(CD81):c.355-3C>T	not provided [RCV005160802]	uncertain significance	11	2395413	2395413	Human		name
597966000	CV3823661	single nucleotide variant	NM_004356.4(CD81):c.460-4G>C	not provided [RCV005165081]	likely benign	11	2395865	2395865	Human		name
597837700	CV3828851	single nucleotide variant	NM_004356.4(CD81):c.66+19G>T	not provided [RCV005171544]	likely benign	11	2377634	2377634	Human		name
14399115	CV614354	single nucleotide variant	NM_004356.4(CD81):c.182-5G>A	Immunodeficiency, common variable, 6 [RCV000768174]\|not provided [RCV003727819]	likely benign\|uncertain significance	11	2394090	2394090	Human	1	name , alternate_id
15164746	CV730760	single nucleotide variant	NM_004356.4(CD81):c.181+8C>T	not provided [RCV000882264]	likely benign	11	2390534	2390534	Human		name
15197887	CV759995	single nucleotide variant	NM_004356.4(CD81):c.562-7C>T	not provided [RCV000912101]	likely benign	11	2396621	2396621	Human		name
15103281	CV775843	single nucleotide variant	NM_004356.4(CD81):c.280-6C>T	not provided [RCV000937166]	likely benign	11	2394966	2394966	Human		name
15138686	CV779538	single nucleotide variant	NM_004356.4(CD81):c.459+4C>T	Immunodeficiency, common variable, 6 [RCV002489383]\|not provided [RCV000965832]	benign\|likely benign	11	2395524	2395524	Human	1	name , alternate_id
127283674	CV1099817	single nucleotide variant	NM_004356.4(CD81):c.182-15C>G	not provided [RCV001448663]	likely benign	11	2394080	2394080	Human		name
127329198	CV1121314	single nucleotide variant	NM_004356.4(CD81):c.355-16C>T	not provided [RCV001470028]	likely benign	11	2395400	2395400	Human		name
127297784	CV1156678	single nucleotide variant	NM_004356.4(CD81):c.279+15C>T	not provided [RCV001513002]	benign	11	2394207	2394207	Human		name
127305070	CV1156680	single nucleotide variant	NM_004356.4(CD81):c.354+17A>G	not provided [RCV001516141]	benign	11	2395063	2395063	Human		name
150511295	CV1212698	single nucleotide variant	NM_004356.4(CD81):c.648+27C>T	not provided [RCV001597929]	benign	11	2396741	2396741	Human		name
150506115	CV1226267	single nucleotide variant	NM_004356.4(CD81):c.67-274G>A	not provided [RCV001635635]	benign	11	2390138	2390138	Human		name
150459661	CV1236126	single nucleotide variant	NM_004356.4(CD81):c.67-106C>T	not provided [RCV001649097]	benign	11	2390306	2390306	Human		name
150498538	CV1255596	single nucleotide variant	NM_004356.4(CD81):c.280-84G>A	not provided [RCV001676384]	benign	11	2394888	2394888	Human		name
150456637	CV1278526	single nucleotide variant	NM_004356.4(CD81):c.561+70G>T	not provided [RCV001709141]	benign	11	2396040	2396040	Human		name
152175633	CV1527003	single nucleotide variant	NM_004356.4(CD81):c.355-14C>T	not provided [RCV002163769]	likely benign	11	2395402	2395402	Human		name
152124047	CV1564001	single nucleotide variant	NM_004356.4(CD81):c.648+20G>C	not provided [RCV002175958]	likely benign	11	2396734	2396734	Human		name
152110944	CV1564150	single nucleotide variant	NM_004356.4(CD81):c.181+19G>T	not provided [RCV002174327]	likely benign	11	2390545	2390545	Human		name
152056208	CV1584050	single nucleotide variant	NM_004356.4(CD81):c.649-17C>T	not provided [RCV002208121]	likely benign	11	2396787	2396787	Human		name
152035137	CV1584820	single nucleotide variant	NM_004356.4(CD81):c.649-14C>T	not provided [RCV002125206]	likely benign	11	2396790	2396790	Human		name
152048790	CV1585439	single nucleotide variant	NM_004356.4(CD81):c.460-12T>C	not provided [RCV002145408]	likely benign	11	2395857	2395857	Human		name
152131178	CV1598001	single nucleotide variant	NM_004356.4(CD81):c.181+18C>G	not provided [RCV002176821]	likely benign	11	2390544	2390544	Human		name
152151893	CV1598379	single nucleotide variant	NM_004356.4(CD81):c.355-12C>T	not provided [RCV002121865]	likely benign	11	2395404	2395404	Human		name
152096559	CV1599731	single nucleotide variant	NM_004356.4(CD81):c.648+17G>A	not provided [RCV002151275]	likely benign	11	2396731	2396731	Human		name
152132728	CV1604838	single nucleotide variant	NM_004356.4(CD81):c.649-19C>T	not provided [RCV002099705]	likely benign	11	2396785	2396785	Human		name
152085370	CV1617269	single nucleotide variant	NM_004356.4(CD81):c.649-16C>A	not provided [RCV002076911]	likely benign	11	2396788	2396788	Human		name
152057706	CV1617330	single nucleotide variant	NM_004356.4(CD81):c.561+12C>T	not provided [RCV002089901]	likely benign	11	2395982	2395982	Human		name
152042111	CV1624179	single nucleotide variant	NM_004356.4(CD81):c.459+18G>A	not provided [RCV002126224]	likely benign	11	2395538	2395538	Human		name
152062660	CV1629843	single nucleotide variant	NM_004356.4(CD81):c.459+12G>T	not provided [RCV002208883]	likely benign	11	2395532	2395532	Human		name
152172360	CV1650712	single nucleotide variant	NM_004356.4(CD81):c.459+16G>A	not provided [RCV002162426]	likely benign	11	2395536	2395536	Human		name
156113632	CV1958028	single nucleotide variant	NM_004356.4(CD81):c.648+16C>T	not provided [RCV002592865]	likely benign	11	2396730	2396730	Human		name
156265780	CV1960859	single nucleotide variant	NM_004356.4(CD81):c.562-11C>A	not provided [RCV002576999]	likely benign	11	2396617	2396617	Human		name
156214846	CV1963226	single nucleotide variant	NM_004356.4(CD81):c.181+19G>A	not provided [RCV002575293]	likely benign	11	2390545	2390545	Human		name
156197656	CV1967852	single nucleotide variant	NM_004356.4(CD81):c.459+10C>T	not provided [RCV002625621]	likely benign	11	2395530	2395530	Human		name
156411757	CV1973692	single nucleotide variant	NM_004356.4(CD81):c.561+13G>A	not provided [RCV002608345]	likely benign	11	2395983	2395983	Human		name
155972718	CV1974735	single nucleotide variant	NM_004356.4(CD81):c.354+13G>A	not provided [RCV002617254]	uncertain significance	11	2395059	2395059	Human		name
156326439	CV1980634	single nucleotide variant	NM_004356.4(CD81):c.648+11G>A	not provided [RCV002630680]	likely benign	11	2396725	2396725	Human		name
156405357	CV1994364	single nucleotide variant	NM_004356.4(CD81):c.182-11C>T	not provided [RCV002658287]	likely benign	11	2394084	2394084	Human		name
156391504	CV1995683	single nucleotide variant	NM_004356.4(CD81):c.459+14G>A	not provided [RCV002680808]	likely benign	11	2395534	2395534	Human		name
156186130	CV1997785	single nucleotide variant	NM_004356.4(CD81):c.181+20C>T	not provided [RCV002643174]	likely benign	11	2390546	2390546	Human		name
156199808	CV2024497	single nucleotide variant	NM_004356.4(CD81):c.355-12C>A	not provided [RCV002711362]	likely benign	11	2395404	2395404	Human		name
155954306	CV2043919	single nucleotide variant	NM_004356.4(CD81):c.562-18G>T	not provided [RCV002775939]	benign	11	2396610	2396610	Human		name
155936703	CV2150002	single nucleotide variant	NM_004356.4(CD81):c.648+17G>T	not provided [RCV003013990]	likely benign	11	2396731	2396731	Human		name
156358992	CV2162303	single nucleotide variant	NM_004356.4(CD81):c.460-11G>A	not provided [RCV003031430]	likely benign	11	2395858	2395858	Human		name
156220178	CV2168249	single nucleotide variant	NM_004356.4(CD81):c.280-10C>T	not provided [RCV003042690]	likely benign	11	2394962	2394962	Human		name
156011795	CV2172288	single nucleotide variant	NM_004356.4(CD81):c.562-16C>T	not provided [RCV003035281]	likely benign	11	2396612	2396612	Human		name
405032838	CV2922657	single nucleotide variant	NM_004356.4(CD81):c.460-18C>T	not provided [RCV003578488]	likely benign	11	2395851	2395851	Human		name
405216249	CV2972032	single nucleotide variant	NM_004356.4(CD81):c.182-18T>C	not provided [RCV003680061]	likely benign	11	2394077	2394077	Human		name
405235905	CV2973270	single nucleotide variant	NM_004356.4(CD81):c.182-20G>C	not provided [RCV003683078]	likely benign	11	2394075	2394075	Human		name
404985182	CV2979717	single nucleotide variant	NM_004356.4(CD81):c.648+15G>C	not provided [RCV003691744]	likely benign	11	2396729	2396729	Human		name
405213974	CV2985118	single nucleotide variant	NM_004356.4(CD81):c.562-18G>A	not provided [RCV003709072]	likely benign	11	2396610	2396610	Human		name
404992729	CV2999558	single nucleotide variant	NM_004356.4(CD81):c.354+19G>A	not provided [RCV003692437]	likely benign	11	2395065	2395065	Human		name
405147801	CV3024162	single nucleotide variant	NM_004356.4(CD81):c.279+19C>A	not provided [RCV003703065]	likely benign	11	2394211	2394211	Human		name
402503530	CV3041775	single nucleotide variant	NM_004356.4(CD81):c.280-18G>A	not provided [RCV003714985]	likely benign	11	2394954	2394954	Human		name
405140510	CV3131166	single nucleotide variant	NM_004356.4(CD81):c.355-10C>T	not provided [RCV003839206]	likely benign	11	2395406	2395406	Human		name
404988089	CV3135612	single nucleotide variant	NM_004356.4(CD81):c.562-20G>A	not provided [RCV003826907]	likely benign	11	2396608	2396608	Human		name
405156920	CV3152549	single nucleotide variant	NM_004356.4(CD81):c.181+11A>G	not provided [RCV003840476]	likely benign	11	2390537	2390537	Human		name
405158656	CV3152615	single nucleotide variant	NM_004356.4(CD81):c.460-10C>T	not provided [RCV003840542]	likely benign	11	2395859	2395859	Human		name
405243221	CV3164636	single nucleotide variant	NM_004356.4(CD81):c.280-14C>T	not provided [RCV003867717]	likely benign	11	2394958	2394958	Human		name
597953704	CV3757102	duplication	NM_004356.4(CD81):c.459+16dup	not provided [RCV005079963]	benign	11	2395530	2395531	Human		name
597960660	CV3794715	single nucleotide variant	NM_004356.4(CD81):c.279+13G>A	not provided [RCV005138620]	likely benign	11	2394205	2394205	Human		name
597950761	CV3815211	single nucleotide variant	NM_004356.4(CD81):c.279+13G>T	not provided [RCV005161161]	likely benign	11	2394205	2394205	Human		name
597881368	CV3826516	single nucleotide variant	NM_004356.4(CD81):c.354+20G>C	not provided [RCV005178213]	likely benign	11	2395066	2395066	Human		name
15148853	CV730761	single nucleotide variant	NM_004356.4(CD81):c.648+10C>T	Immunodeficiency, common variable, 6 [RCV003626644]\|not provided [RCV000879040]	benign\|likely benign	11	2396724	2396724	Human	1	name , alternate_id
150331531	CV1172241	single nucleotide variant	NM_004356.4(CD81):c.459+134T>G	not provided [RCV001538669]	benign	11	2395654	2395654	Human		name
150450256	CV1215224	single nucleotide variant	NM_004356.4(CD81):c.459+148C>T	not provided [RCV001611814]	benign	11	2395668	2395668	Human		name
150469712	CV1243202	single nucleotide variant	NM_004356.4(CD81):c.459+172G>C	not provided [RCV001650722]	benign	11	2395692	2395692	Human		name
150493438	CV1257554	single nucleotide variant	NM_004356.4(CD81):c.280-238G>A	not provided [RCV001675227]	benign	11	2394734	2394734	Human		name
150444565	CV1258537	single nucleotide variant	NM_004356.4(CD81):c.280-216G>A	not provided [RCV001679735]	benign	11	2394756	2394756	Human		name
150452093	CV1260345	single nucleotide variant	NM_004356.4(CD81):c.181+240T>C	not provided [RCV001680835]	benign	11	2390766	2390766	Human		name
150477883	CV1281761	single nucleotide variant	NM_004356.4(CD81):c.561+323A>G	not provided [RCV001714200]	benign	11	2396293	2396293	Human		name
152174940	CV1520565	microsatellite	NM_004356.4(CD81):c.182-16TC[3]	not provided [RCV002184682]	likely benign	11	2394079	2394080	Human		name
150454991	CV1266113	single nucleotide variant	NM_001297649.2(CD81):c.-148+835T>C	not provided [RCV001692690]	benign	11	2377192	2377192	Human		name
151720977	CV1504494	single nucleotide variant	NM_004356.4(CD81):c.9G>C (p.Val3=)	CD81-related disorder [RCV003893021]\|not provided [RCV001983075]	likely benign	11	2377558	2377558	Human	1	name , trait , alternate_id
156407438	CV1918118	single nucleotide variant	NM_004356.4(CD81):c.27C>T (p.Cys9=)	not provided [RCV002606894]	likely benign	11	2377576	2377576	Human		name
127319230	CV1156677	single nucleotide variant	NM_004356.4(CD81):c.78C>A (p.Gly26=)	not provided [RCV001522037]	benign	11	2390423	2390423	Human		name
151737931	CV1358414	single nucleotide variant	NM_004356.4(CD81):c.69G>A (p.Leu23=)	not provided [RCV001967843]	uncertain significance	11	2390414	2390414	Human		name
152061012	CV1557522	single nucleotide variant	NM_004356.4(CD81):c.87G>C (p.Leu29=)	not provided [RCV002146775]	likely benign	11	2390432	2390432	Human		name
152145242	CV1576684	single nucleotide variant	NM_004356.4(CD81):c.96C>A (p.Ala32=)	not provided [RCV002101361]	likely benign	11	2390441	2390441	Human		name
152055414	CV1633195	single nucleotide variant	NM_004356.4(CD81):c.37C>T (p.Leu13=)	not provided [RCV002127714]	likely benign	11	2377586	2377586	Human		name
156340569	CV2179782	single nucleotide variant	NM_004356.4(CD81):c.48C>G (p.Val16=)	not provided [RCV003030262]	likely benign	11	2377597	2377597	Human		name
405253894	CV3044941	single nucleotide variant	NM_004356.4(CD81):c.60C>T (p.Val20=)	not provided [RCV003722666]	likely benign	11	2377609	2377609	Human		name
402474984	CV3182847	single nucleotide variant	NM_004356.4(CD81):c.78C>T (p.Gly26=)	not provided [RCV003875091]	likely benign	11	2390423	2390423	Human		name
597915300	CV3778995	single nucleotide variant	NM_004356.4(CD81):c.84C>T (p.Ile28=)	not provided [RCV005129340]	likely benign	11	2390429	2390429	Human		name
597867479	CV3803012	single nucleotide variant	NM_004356.4(CD81):c.7G>C (p.Val3Leu)	not provided [RCV005147799]	uncertain significance	11	2377556	2377556	Human		name
597928234	CV3816109	single nucleotide variant	NM_004356.4(CD81):c.72T>G (p.Ala24=)	not provided [RCV005156690]	likely benign	11	2390417	2390417	Human		name
597862908	CV3822733	single nucleotide variant	NM_004356.4(CD81):c.42C>G (p.Leu14=)	not provided [RCV005175265]	likely benign	11	2377591	2377591	Human		name
127305537	CV1156679	single nucleotide variant	NM_004356.4(CD81):c.288C>T (p.Thr96=)	CD81-related disorder [RCV003931091]\|not provided [RCV001516318]	benign	11	2394980	2394980	Human	1	name , trait , alternate_id
151714541	CV1477182	single nucleotide variant	NM_004356.4(CD81):c.11A>G (p.Glu4Gly)	not provided [RCV001908700]	uncertain significance	11	2377560	2377560	Human		name
152080391	CV1550118	single nucleotide variant	NM_004356.4(CD81):c.195C>T (p.Leu65=)	not provided [RCV002192948]	likely benign	11	2394108	2394108	Human		name
152143736	CV1582415	single nucleotide variant	NM_004356.4(CD81):c.222C>T (p.Phe74=)	not provided [RCV002200916]	benign	11	2394135	2394135	Human		name
152070401	CV1628388	single nucleotide variant	NM_004356.4(CD81):c.207C>T (p.Gly69=)	not provided [RCV002169214]	likely benign	11	2394120	2394120	Human		name
152100756	CV1645654	single nucleotide variant	NM_004356.4(CD81):c.198C>T (p.Ile66=)	not provided [RCV002173067]	likely benign	11	2394111	2394111	Human		name
152173329	CV1653039	single nucleotide variant	NM_004356.4(CD81):c.159C>T (p.Pro53=)	Immunodeficiency, common variable, 6 [RCV002500300]\|not provided [RCV002144069]	likely benign	11	2390504	2390504	Human	1	name , alternate_id
156332126	CV1954175	single nucleotide variant	NM_004356.4(CD81):c.177T>C (p.Tyr59=)	not provided [RCV002580058]	likely benign	11	2390522	2390522	Human		name
155956060	CV2162661	single nucleotide variant	NM_004356.4(CD81):c.26G>A (p.Cys9Tyr)	not provided [RCV003015106]	uncertain significance	11	2377575	2377575	Human		name
405081439	CV2854759	single nucleotide variant	NM_004356.4(CD81):c.105C>G (p.Leu35=)	not provided [RCV003549153]	likely benign	11	2390450	2390450	Human		name
405065599	CV2879135	single nucleotide variant	NM_004356.4(CD81):c.232C>T (p.Leu78=)	not provided [RCV003548217]	likely benign	11	2394145	2394145	Human		name
405178542	CV2952119	single nucleotide variant	NM_004356.4(CD81):c.291C>T (p.Cys97=)	not provided [RCV003675979]	likely benign	11	2394983	2394983	Human		name
405187950	CV3069032	single nucleotide variant	NM_004356.4(CD81):c.123C>T (p.Thr41=)	not provided [RCV003729448]	likely benign	11	2390468	2390468	Human		name
405213288	CV3142781	single nucleotide variant	NM_004356.4(CD81):c.171C>T (p.Thr57=)	not provided [RCV003846139]	likely benign	11	2390516	2390516	Human		name
402479172	CV3170183	single nucleotide variant	NM_004356.4(CD81):c.23A>G (p.Lys8Arg)	not provided [RCV003875571]	uncertain significance	11	2377572	2377572	Human		name
402484029	CV3171224	single nucleotide variant	NM_004356.4(CD81):c.162G>A (p.Ala54=)	not provided [RCV003876251]	likely benign	11	2390507	2390507	Human		name
597911291	CV3745597	single nucleotide variant	NM_004356.4(CD81):c.210T>C (p.Ala70=)	not provided [RCV005073598]	likely benign	11	2394123	2394123	Human		name
597869089	CV3764568	single nucleotide variant	NM_004356.4(CD81):c.276G>T (p.Gly92=)	not provided [RCV005107368]	uncertain significance	11	2394189	2394189	Human		name
597897054	CV3806761	single nucleotide variant	NM_004356.4(CD81):c.225T>G (p.Val75=)	not provided [RCV005152148]	likely benign	11	2394138	2394138	Human		name
597915010	CV3817611	single nucleotide variant	NM_004356.4(CD81):c.243C>T (p.Tyr81=)	not provided [RCV005154813]	likely benign	11	2394156	2394156	Human		name
15192109	CV737923	single nucleotide variant	NM_004356.4(CD81):c.126C>G (p.Thr42=)	not provided [RCV000910441]	likely benign	11	2390471	2390471	Human		name
15139668	CV737924	single nucleotide variant	NM_004356.4(CD81):c.273G>A (p.Leu91=)	CD81-related disorder [RCV003958111]\|not provided [RCV000899184]	likely benign	11	2394186	2394186	Human	1	name , trait , alternate_id
127279566	CV1078136	single nucleotide variant	NM_004356.4(CD81):c.636C>T (p.Val212=)	not provided [RCV001409213]	likely benign	11	2396702	2396702	Human		name
127320592	CV1156681	single nucleotide variant	NM_004356.4(CD81):c.639T>C (p.Ala213=)	not provided [RCV001522710]	benign	11	2396705	2396705	Human		name
151235367	CV1318645	single nucleotide variant	NM_004356.4(CD81):c.426C>T (p.Asn142=)	not provided [RCV001794975]	likely benign	11	2395487	2395487	Human		name
151763252	CV1471568	single nucleotide variant	NM_004356.4(CD81):c.630C>T (p.Ile210=)	not provided [RCV001949395]	likely benign	11	2396696	2396696	Human		name
151745833	CV1485107	single nucleotide variant	NM_004356.4(CD81):c.531G>A (p.Ser177=)	not provided [RCV002006297]	likely benign\|uncertain significance	11	2395940	2395940	Human		name
152145617	CV1543306	single nucleotide variant	NM_004356.4(CD81):c.621T>C (p.Ile207=)	not provided [RCV002178680]	likely benign	11	2396687	2396687	Human		name
152076009	CV1551331	single nucleotide variant	NM_004356.4(CD81):c.363G>A (p.Lys121=)	not provided [RCV002192415]	likely benign	11	2395424	2395424	Human		name
152158491	CV1553053	single nucleotide variant	NM_004356.4(CD81):c.664C>T (p.Leu222=)	not provided [RCV002180500]	likely benign	11	2396819	2396819	Human		name
152123627	CV1563821	single nucleotide variant	NM_004356.4(CD81):c.303G>T (p.Leu101=)	not provided [RCV002175908]	likely benign	11	2394995	2394995	Human		name
152078729	CV1602180	single nucleotide variant	NM_004356.4(CD81):c.702C>T (p.Ser234=)	not provided [RCV002149027]	likely benign	11	2396857	2396857	Human		name
152079473	CV1620564	single nucleotide variant	NM_004356.4(CD81):c.615C>T (p.Ile205=)	not provided [RCV002112554]	likely benign	11	2396681	2396681	Human		name
152157128	CV1629804	single nucleotide variant	NM_004356.4(CD81):c.702C>A (p.Ser234=)	not provided [RCV002202783]	likely benign	11	2396857	2396857	Human		name
152114968	CV1640888	single nucleotide variant	NM_004356.4(CD81):c.411T>C (p.Asp137=)	CD81-related disorder [RCV003958660]\|not provided [RCV002117057]	likely benign	11	2395472	2395472	Human	1	name , trait , alternate_id
152040265	CV1649161	single nucleotide variant	NM_004356.4(CD81):c.324C>T (p.Ala108=)	not provided [RCV002206240]	likely benign	11	2395016	2395016	Human		name
156445039	CV1949096	single nucleotide variant	NM_004356.4(CD81):c.579G>A (p.Lys193=)	not provided [RCV003115973]	likely benign	11	2396645	2396645	Human		name
156079257	CV1959764	single nucleotide variant	NM_004356.4(CD81):c.705G>T (p.Val235=)	not provided [RCV002569854]	likely benign	11	2396860	2396860	Human		name
156266167	CV1973874	single nucleotide variant	NM_004356.4(CD81):c.417C>T (p.Asp139=)	CD81-related disorder [RCV003971335]\|not provided [RCV002597941]	likely benign	11	2395478	2395478	Human	1	name , trait , alternate_id
155912864	CV1980313	single nucleotide variant	NM_004356.4(CD81):c.669C>T (p.Ser223=)	CD81-related disorder [RCV003973447]\|not provided [RCV002614116]	likely benign	11	2396824	2396824	Human	1	name , trait , alternate_id
155916477	CV2156115	single nucleotide variant	NM_004356.4(CD81):c.600G>A (p.Gly200=)	not provided [RCV002991685]	likely benign	11	2396666	2396666	Human		name
156361111	CV2180357	single nucleotide variant	NM_004356.4(CD81):c.522G>A (p.Leu174=)	not provided [RCV003049029]	likely benign	11	2395931	2395931	Human		name
156239745	CV2188793	single nucleotide variant	NM_004356.4(CD81):c.71C>T (p.Ala24Val)	not provided [RCV003059615]	uncertain significance	11	2390416	2390416	Human		name
401910023	CV2806669	single nucleotide variant	NM_004356.4(CD81):c.585T>C (p.Asp195=)	not provided [RCV003424766]	likely benign	11	2396651	2396651	Human		name
405211431	CV2868060	single nucleotide variant	NM_004356.4(CD81):c.429C>T (p.Ala143=)	not provided [RCV003552655]	likely benign	11	2395490	2395490	Human		name
405194310	CV2872428	single nucleotide variant	NM_004356.4(CD81):c.402C>G (p.Ala134=)	not provided [RCV003550695]	likely benign	11	2395463	2395463	Human		name
405205856	CV2873787	single nucleotide variant	NM_004356.4(CD81):c.591C>G (p.Leu197=)	not provided [RCV003551931]	likely benign	11	2396657	2396657	Human		name
404983303	CV2989644	single nucleotide variant	NM_004356.4(CD81):c.342C>T (p.Val114=)	not provided [RCV003691537]	likely benign	11	2395034	2395034	Human		name
405225734	CV2989795	single nucleotide variant	NM_004356.4(CD81):c.315G>A (p.Glu105=)	not provided [RCV003681387]	likely benign	11	2395007	2395007	Human		name
405088039	CV3044495	single nucleotide variant	NM_004356.4(CD81):c.49T>C (p.Phe17Leu)	not provided [RCV003717615]\|not specified [RCV004897813]	uncertain significance	11	2377598	2377598	Human		name
405208938	CV3065552	single nucleotide variant	NM_004356.4(CD81):c.474C>T (p.Gly158=)	not provided [RCV003731711]	likely benign	11	2395883	2395883	Human		name
404992979	CV3132430	single nucleotide variant	NM_004356.4(CD81):c.402C>T (p.Ala134=)	not provided [RCV003827369]	likely benign	11	2395463	2395463	Human		name
405235138	CV3155904	single nucleotide variant	NM_004356.4(CD81):c.95C>G (p.Ala32Gly)	not provided [RCV003853637]	uncertain significance	11	2390440	2390440	Human		name
402498694	CV3170348	single nucleotide variant	NM_004356.4(CD81):c.676C>T (p.Leu226=)	not provided [RCV003877720]	likely benign	11	2396831	2396831	Human		name
597947462	CV3758969	single nucleotide variant	NM_004356.4(CD81):c.300C>A (p.Ile100=)	not provided [RCV005078765]	likely benign	11	2394992	2394992	Human		name
597952961	CV3798867	single nucleotide variant	NM_004356.4(CD81):c.40C>T (p.Leu14Phe)	not provided [RCV005136441]	uncertain significance	11	2377589	2377589	Human		name
597924721	CV3808685	single nucleotide variant	NM_004356.4(CD81):c.693G>C (p.Arg231=)	not provided [RCV005156199]	likely benign	11	2396848	2396848	Human		name
597892868	CV3833349	single nucleotide variant	NM_004356.4(CD81):c.483A>T (p.Thr161=)	not provided [RCV005180041]	likely benign	11	2395892	2395892	Human		name
13436821	CV433404	single nucleotide variant	NM_004356.4(CD81):c.414T>C (p.Asp138=)	Immunodeficiency, common variable, 6 [RCV002490849]\|not provided [RCV000969792]\|not specified [RCV000507825]	benign\|likely benign	11	2395475	2395475	Human	1	name , alternate_id
15130366	CV712770	single nucleotide variant	NM_004356.4(CD81):c.654C>T (p.Phe218=)	not provided [RCV000964423]	likely benign	11	2396809	2396809	Human		name
15148849	CV724370	single nucleotide variant	NM_004356.4(CD81):c.453C>T (p.His151=)	not provided [RCV000879039]	benign	11	2395514	2395514	Human		name
15140094	CV783974	single nucleotide variant	NM_004356.4(CD81):c.357C>T (p.Ile119=)	not provided [RCV000982756]	likely benign	11	2395418	2395418	Human		name
21405396	CV799641	single nucleotide variant	NM_004356.4(CD81):c.597C>T (p.Ser199=)	Immunodeficiency, common variable, 6 [RCV001000331]\|not provided [RCV001522709]	benign	11	2396663	2396663	Human	1	name , alternate_id
151859892	CV1452185	single nucleotide variant	NM_004356.4(CD81):c.199G>A (p.Ala67Thr)	not provided [RCV002017627]	uncertain significance	11	2394112	2394112	Human		name
156248203	CV1948941	single nucleotide variant	NM_004356.4(CD81):c.144G>T (p.Glu48Asp)	not provided [RCV003111670]\|not specified [RCV004102973]	uncertain significance	11	2390489	2390489	Human		name
155904186	CV1975879	single nucleotide variant	NM_004356.4(CD81):c.211G>A (p.Val71Ile)	not provided [RCV002613574]	uncertain significance	11	2394124	2394124	Human		name
156321751	CV1992059	single nucleotide variant	NM_004356.4(CD81):c.128A>G (p.Asn43Ser)	not provided [RCV002649292]\|not specified [RCV004897760]	uncertain significance	11	2390473	2390473	Human		name
156113739	CV1993775	single nucleotide variant	NM_004356.4(CD81):c.106C>T (p.Arg36Cys)	not provided [RCV002662589]	uncertain significance	11	2390451	2390451	Human		name
156207198	CV2007900	single nucleotide variant	NM_004356.4(CD81):c.124A>G (p.Thr42Ala)	not provided [RCV002700491]	uncertain significance	11	2390469	2390469	Human		name
155992831	CV2063839	single nucleotide variant	NM_004356.4(CD81):c.122C>A (p.Thr41Asn)	not provided [RCV002843038]	uncertain significance	11	2390467	2390467	Human		name
156153999	CV2175545	single nucleotide variant	NM_004356.4(CD81):c.227G>C (p.Gly76Ala)	not provided [RCV003040467]	uncertain significance	11	2394140	2394140	Human		name
405077584	CV2869668	single nucleotide variant	NM_004356.4(CD81):c.242A>G (p.Tyr81Cys)	not provided [RCV003548915]	uncertain significance	11	2394155	2394155	Human		name
402523450	CV2940370	single nucleotide variant	NM_004356.4(CD81):c.107G>A (p.Arg36His)	not provided [RCV003663480]	uncertain significance	11	2390452	2390452	Human		name
405119497	CV2957529	single nucleotide variant	NM_004356.4(CD81):c.190A>G (p.Ile64Val)	not provided [RCV003667289]	uncertain significance	11	2394103	2394103	Human		name
405131973	CV2959159	single nucleotide variant	NM_004356.4(CD81):c.116C>T (p.Pro39Leu)	not provided [RCV003668460]\|not specified [RCV004371608]	uncertain significance	11	2390461	2390461	Human		name
405218977	CV2968847	deletion	NM_004356.4(CD81):c.508del (p.Leu170fs)	not provided [RCV003680398]	uncertain significance	11	2395917	2395917	Human		name
404982807	CV2979541	single nucleotide variant	NM_004356.4(CD81):c.145C>A (p.Leu49Met)	not provided [RCV003691482]	uncertain significance	11	2390490	2390490	Human		name
405174126	CV3023413	single nucleotide variant	NM_004356.4(CD81):c.110A>T (p.His37Leu)	not provided [RCV003704943]	uncertain significance	11	2390455	2390455	Human		name
405198519	CV3032834	single nucleotide variant	NM_004356.4(CD81):c.155A>G (p.Lys52Arg)	not provided [RCV003707207]	uncertain significance	11	2390500	2390500	Human		name
405126288	CV3132695	single nucleotide variant	NM_004356.4(CD81):c.278C>T (p.Thr93Met)	not provided [RCV003837858]	uncertain significance	11	2394191	2394191	Human		name
405107630	CV3136268	single nucleotide variant	NM_004356.4(CD81):c.152A>G (p.Asp51Gly)	not provided [RCV003835614]	uncertain significance	11	2390497	2390497	Human		name
405202244	CV3143544	single nucleotide variant	NM_004356.4(CD81):c.160G>A (p.Ala54Thr)	not provided [RCV003844530]	uncertain significance	11	2390505	2390505	Human		name
405210625	CV3158966	single nucleotide variant	NM_004356.4(CD81):c.275G>A (p.Gly92Glu)	not provided [RCV003862087]	uncertain significance	11	2394188	2394188	Human		name
404994936	CV3176599	single nucleotide variant	NM_004356.4(CD81):c.161C>T (p.Ala54Val)	not provided [RCV003882031]	uncertain significance	11	2390506	2390506	Human		name
597931864	CV3780419	single nucleotide variant	NM_004356.4(CD81):c.295G>A (p.Val99Ile)	not provided [RCV005116739]	uncertain significance	11	2394987	2394987	Human		name
598166703	CV3950838	single nucleotide variant	NM_004356.4(CD81):c.125C>T (p.Thr42Ile)	not specified [RCV005307930]	uncertain significance	11	2390470	2390470	Human		name
14699357	CV624425	single nucleotide variant	NM_004356.4(CD81):c.119A>G (p.Gln40Arg)	not provided [RCV000788681]	uncertain significance	11	2390464	2390464	Human		name
151734756	CV1393257	single nucleotide variant	NM_004356.4(CD81):c.631G>A (p.Val211Met)	not provided [RCV001967482]	uncertain significance	11	2396697	2396697	Human		name
151765725	CV1393763	single nucleotide variant	NM_004356.4(CD81):c.699C>A (p.Ser233Arg)	not provided [RCV002008357]	uncertain significance	11	2396854	2396854	Human		name
151794271	CV1394952	single nucleotide variant	NM_004356.4(CD81):c.427G>A (p.Ala143Thr)	not provided [RCV001973336]	uncertain significance	11	2395488	2395488	Human		name
151741538	CV1404875	single nucleotide variant	NM_004356.4(CD81):c.445A>C (p.Thr149Pro)	not provided [RCV001947146]	uncertain significance	11	2395506	2395506	Human		name
151743488	CV1406749	single nucleotide variant	NM_004356.4(CD81):c.403G>A (p.Val135Met)	not provided [RCV002006052]	uncertain significance	11	2395464	2395464	Human		name
151880742	CV1421558	single nucleotide variant	NM_004356.4(CD81):c.533G>A (p.Gly178Asp)	not provided [RCV001886443]	uncertain significance	11	2395942	2395942	Human		name
151804471	CV1432334	single nucleotide variant	NM_004356.4(CD81):c.418G>A (p.Ala140Thr)	not provided [RCV001991251]	uncertain significance	11	2395479	2395479	Human		name
151735299	CV1435551	single nucleotide variant	NM_004356.4(CD81):c.422A>G (p.Asn141Ser)	not provided [RCV001946498]\|not specified [RCV005321005]	uncertain significance	11	2395483	2395483	Human		name
151769299	CV1441870	single nucleotide variant	NM_004356.4(CD81):c.660G>C (p.Met220Ile)	not provided [RCV002025198]	uncertain significance	11	2396815	2396815	Human		name
151736248	CV1465968	single nucleotide variant	NM_004356.4(CD81):c.409G>A (p.Asp137Asn)	Immunodeficiency, common variable, 6 [RCV003146252]\|not provided [RCV002041747]\|not specified [RCV004038767]	uncertain significance	11	2395470	2395470	Human	1	name , alternate_id
151713740	CV1476728	single nucleotide variant	NM_004356.4(CD81):c.353A>G (p.Gln118Arg)	not provided [RCV001908537]	uncertain significance	11	2395045	2395045	Human		name
151865908	CV1477624	single nucleotide variant	NM_004356.4(CD81):c.439G>A (p.Val147Met)	not provided [RCV001939157]	uncertain significance	11	2395500	2395500	Human		name
151839290	CV1487558	single nucleotide variant	NM_004356.4(CD81):c.392T>G (p.Leu131Arg)	not provided [RCV001935909]	uncertain significance	11	2395453	2395453	Human		name
151829003	CV1489234	single nucleotide variant	NM_004356.4(CD81):c.518A>G (p.Asn173Ser)	not provided [RCV001934873]\|not specified [RCV004039839]	likely benign\|uncertain significance	11	2395927	2395927	Human		name
151721661	CV1491759	single nucleotide variant	NM_004356.4(CD81):c.535A>G (p.Ser179Gly)	not provided [RCV002003762]	uncertain significance	11	2395944	2395944	Human		name
151868058	CV1492008	single nucleotide variant	NM_004356.4(CD81):c.351C>A (p.Asp117Glu)	not provided [RCV002018592]	uncertain significance	11	2395043	2395043	Human		name
155748241	CV1772170	single nucleotide variant	NM_004356.4(CD81):c.544A>C (p.Ile182Leu)	not provided [RCV002303780]	uncertain significance	11	2395953	2395953	Human		name
155728359	CV1776194	single nucleotide variant	NM_004356.4(CD81):c.685G>A (p.Gly229Ser)	not provided [RCV002301598]	uncertain significance	11	2396840	2396840	Human		name
156019671	CV1909405	single nucleotide variant	NM_004356.4(CD81):c.325G>A (p.Gly109Ser)	not provided [RCV002619329]	uncertain significance	11	2395017	2395017	Human		name
156180188	CV1978800	single nucleotide variant	NM_004356.4(CD81):c.616G>A (p.Gly206Ser)	not provided [RCV002595039]	uncertain significance	11	2396682	2396682	Human		name
156311389	CV2000104	single nucleotide variant	NM_004356.4(CD81):c.704T>G (p.Val235Gly)	not provided [RCV002671656]	uncertain significance	11	2396859	2396859	Human		name
156104603	CV2008318	single nucleotide variant	NM_004356.4(CD81):c.344A>G (p.Asn115Ser)	not provided [RCV002695432]	uncertain significance	11	2395036	2395036	Human		name
156029016	CV2039769	single nucleotide variant	NM_004356.4(CD81):c.584A>G (p.Asp195Gly)	not provided [RCV002781031]	uncertain significance	11	2396650	2396650	Human		name
155955809	CV2069969	single nucleotide variant	NM_004356.4(CD81):c.698G>A (p.Ser233Asn)	not provided [RCV002816508]	uncertain significance	11	2396853	2396853	Human		name
155937554	CV2114298	single nucleotide variant	NM_004356.4(CD81):c.552C>A (p.Asn184Lys)	not provided [RCV002904245]	uncertain significance	11	2395961	2395961	Human		name
156372885	CV2127681	single nucleotide variant	NM_004356.4(CD81):c.473G>A (p.Gly158Asp)	not provided [RCV002942476]	uncertain significance	11	2395882	2395882	Human		name
156162311	CV2136886	single nucleotide variant	NM_004356.4(CD81):c.511A>G (p.Lys171Glu)	not provided [RCV003005112]	uncertain significance	11	2395920	2395920	Human		name
155906028	CV2148103	single nucleotide variant	NM_004356.4(CD81):c.670A>G (p.Met224Val)	not provided [RCV003011927]	uncertain significance	11	2396825	2396825	Human		name
155998875	CV2296133	single nucleotide variant	NM_004356.4(CD81):c.542T>A (p.Ile181Asn)	not specified [RCV004154063]	uncertain significance	11	2395951	2395951	Human		name
155927552	CV2391407	single nucleotide variant	NM_004356.4(CD81):c.598G>A (p.Gly200Arg)	not specified [RCV004239810]	uncertain significance	11	2396664	2396664	Human		name
243054868	CV2409799	single nucleotide variant	NM_004356.4(CD81):c.352C>T (p.Gln118Ter)	Immunodeficiency, common variable, 6 [RCV003144720]	uncertain significance	11	2395044	2395044	Human	1	name , alternate_id
401900021	CV2780188	single nucleotide variant	NM_004356.4(CD81):c.689T>C (p.Ile230Thr)	not specified [RCV004355836]	uncertain significance	11	2396844	2396844	Human		name
405236497	CV2884642	single nucleotide variant	NM_004356.4(CD81):c.588C>A (p.Asp196Glu)	not provided [RCV003556508]	uncertain significance	11	2396654	2396654	Human		name
405160208	CV2950243	single nucleotide variant	NM_004356.4(CD81):c.444G>T (p.Lys148Asn)	not provided [RCV003674627]	uncertain significance	11	2395505	2395505	Human		name
405186821	CV2977527	single nucleotide variant	NM_004356.4(CD81):c.582C>G (p.Ile194Met)	not provided [RCV003706093]	uncertain significance	11	2396648	2396648	Human		name
402497566	CV2988771	single nucleotide variant	NM_004356.4(CD81):c.599G>A (p.Gly200Glu)	not provided [RCV003714338]	uncertain significance	11	2396665	2396665	Human		name
404980598	CV3006123	single nucleotide variant	NM_004356.4(CD81):c.703G>C (p.Val235Leu)	not provided [RCV003691149]	uncertain significance	11	2396858	2396858	Human		name
405173294	CV3026861	single nucleotide variant	NM_004356.4(CD81):c.566A>T (p.Asp189Val)	not provided [RCV003704875]	uncertain significance	11	2396632	2396632	Human		name
405148166	CV3067286	single nucleotide variant	NM_004356.4(CD81):c.530C>T (p.Ser177Leu)	not provided [RCV003726130]	uncertain significance	11	2395939	2395939	Human		name
405034245	CV3130452	single nucleotide variant	NM_004356.4(CD81):c.375G>T (p.Gln125His)	not provided [RCV003830859]	uncertain significance	11	2395436	2395436	Human		name
405185907	CV3149016	single nucleotide variant	NM_004356.4(CD81):c.660G>A (p.Met220Ile)	not provided [RCV003842939]	uncertain significance	11	2396815	2396815	Human		name
405223330	CV3151141	single nucleotide variant	NM_004356.4(CD81):c.692G>A (p.Arg231Gln)	not provided [RCV003847566]\|not specified [RCV004605062]	uncertain significance	11	2396847	2396847	Human		name
405232897	CV3157603	single nucleotide variant	NM_004356.4(CD81):c.445A>G (p.Thr149Ala)	not provided [RCV003865553]	uncertain significance	11	2395506	2395506	Human		name
597723454	CV3720194	single nucleotide variant	NM_004356.4(CD81):c.423C>G (p.Asn141Lys)	Immunodeficiency, common variable, 6 [RCV005050104]\|not provided [RCV005105376]	uncertain significance	11	2395484	2395484	Human	1	name , alternate_id
597897962	CV3744614	single nucleotide variant	NM_004356.4(CD81):c.403G>C (p.Val135Leu)	not provided [RCV005071893]	uncertain significance	11	2395464	2395464	Human		name
597924882	CV3748540	single nucleotide variant	NM_004356.4(CD81):c.703G>A (p.Val235Met)	not provided [RCV005075188]	uncertain significance	11	2396858	2396858	Human		name
597873110	CV3765956	single nucleotide variant	NM_004356.4(CD81):c.350A>G (p.Asp117Gly)	not provided [RCV005108087]	uncertain significance	11	2395042	2395042	Human		name
597939663	CV3788569	single nucleotide variant	NM_004356.4(CD81):c.298A>G (p.Ile100Val)	not provided [RCV005133244]	uncertain significance	11	2394990	2394990	Human		name
597895811	CV3810455	single nucleotide variant	NM_004356.4(CD81):c.623C>T (p.Ala208Val)	not provided [RCV005151980]	uncertain significance	11	2396689	2396689	Human		name
597919337	CV3811635	single nucleotide variant	NM_004356.4(CD81):c.709T>C (p.Ter237Arg)	not provided [RCV005155466]	uncertain significance	11	2396864	2396864	Human		name
597969236	CV3821437	single nucleotide variant	NM_004356.4(CD81):c.551A>G (p.Asn184Ser)	not provided [RCV005166079]	uncertain significance	11	2395960	2395960	Human		name
597952131	CV3847556	single nucleotide variant	NM_004356.4(CD81):c.322G>A (p.Ala108Thr)	not provided [RCV005190538]	uncertain significance	11	2395014	2395014	Human		name
598166687	CV3950836	single nucleotide variant	NM_004356.4(CD81):c.613A>G (p.Ile205Val)	not specified [RCV005307928]	uncertain significance	11	2396679	2396679	Human		name
598166695	CV3950837	single nucleotide variant	NM_004356.4(CD81):c.655G>A (p.Glu219Lys)	not specified [RCV005307929]	uncertain significance	11	2396810	2396810	Human		name
14699358	CV624426	single nucleotide variant	NM_004356.4(CD81):c.358G>A (p.Ala120Thr)	not provided [RCV000788682]	uncertain significance	11	2395419	2395419	Human		name
21073816	CV796558	single nucleotide variant	NM_004356.4(CD81):c.556T>C (p.Phe186Leu)	not provided [RCV000994549]	uncertain significance	11	2395965	2395965	Human		name
41406581	CV980466	single nucleotide variant	NM_004356.4(CD81):c.583G>A (p.Asp195Asn)	Immunodeficiency, common variable, 6 [RCV001281057]\|not provided [RCV001871628]\|not specified [RCV004035518]	uncertain significance	11	2396649	2396649	Human	1	name , alternate_id
151864083	CV1374565	deletion	NM_004356.4(CD81):c.634_635del (p.Val212fs)	not provided [RCV001884320]	uncertain significance	11	2396700	2396701	Human		name

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