Slc26a8 Variant Search Result - Rat Genome Database

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131 records found for search term Slc26a8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150453522	CV1219843	single nucleotide variant	NM_052961.4(SLC26A8):c.943-95C>G	not provided [RCV001612224]	benign	6	35982298	35982298	Human		name
150436199	CV1249655	single nucleotide variant	NM_052961.4(SLC26A8):c.188+75T>C	not provided [RCV001665569]	benign	6	36019445	36019445	Human		name
150453601	CV1260538	single nucleotide variant	NM_052961.4(SLC26A8):c.-2-159A>G	not provided [RCV001681030]	benign	6	36019868	36019868	Human		name
408386085	CV3521964	single nucleotide variant	NM_052961.4(SLC26A8):c.1639-2A>G	Spermatogenic failure 3 [RCV004760289]	uncertain significance	6	35959808	35959808	Human	1	name
15165585	CV779251	single nucleotide variant	NM_052961.4(SLC26A8):c.1731+8C>G	not provided [RCV000970982]	benign	6	35959706	35959706	Human		name
15133728	CV779348	single nucleotide variant	NM_052961.4(SLC26A8):c.1174-4A>G	not provided [RCV000965003]	benign	6	35975492	35975492	Human		name
150336940	CV1171569	single nucleotide variant	NM_052961.4(SLC26A8):c.942+218A>C	not provided [RCV001541293]	benign	6	35991441	35991441	Human		name
150492436	CV1225473	single nucleotide variant	NM_052961.4(SLC26A8):c.446-114G>A	not provided [RCV001618988]	benign	6	35998033	35998033	Human		name
150506996	CV1226482	single nucleotide variant	NM_052961.4(SLC26A8):c.627+150G>A	not provided [RCV001635850]	benign	6	35997588	35997588	Human		name
150517243	CV1226691	single nucleotide variant	NM_052961.4(SLC26A8):c.446-173A>T	not provided [RCV001639785]	benign	6	35998092	35998092	Human		name
150516389	CV1228332	single nucleotide variant	NM_052961.4(SLC26A8):c.943-230A>G	not provided [RCV001639138]	benign	6	35982433	35982433	Human		name
150473630	CV1252438	single nucleotide variant	NM_052961.4(SLC26A8):c.942+275C>T	not provided [RCV001671640]	benign	6	35991384	35991384	Human		name
150481172	CV1258868	single nucleotide variant	NM_052961.4(SLC26A8):c.628-163G>A	not provided [RCV001685998]	benign	6	35992837	35992837	Human		name
150476720	CV1263687	single nucleotide variant	NM_052961.4(SLC26A8):c.627+305G>A	not provided [RCV001685210]	benign	6	35997433	35997433	Human		name
150445612	CV1269463	single nucleotide variant	NM_052961.4(SLC26A8):c.329-215A>G	not provided [RCV001691151]	benign	6	36000323	36000323	Human		name
150506616	CV1210966	duplication	NM_052961.4(SLC26A8):c.1026-107dup	not provided [RCV001596084]	benign	6	35977442	35977443	Human		name
150480662	CV1222013	single nucleotide variant	NM_052961.4(SLC26A8):c.1026-215G>A	not provided [RCV001616810]	benign	6	35977566	35977566	Human		name
150471518	CV1270092	single nucleotide variant	NM_052961.4(SLC26A8):c.2473-152T>C	not provided [RCV001695380]	benign	6	35944492	35944492	Human		name
150450279	CV1275788	single nucleotide variant	NM_052961.4(SLC26A8):c.1639-195G>A	not provided [RCV001708243]	benign	6	35960001	35960001	Human		name
150454207	CV1265965	microsatellite	NM_052961.4(SLC26A8):c.2473-184ATT[3]	not provided [RCV001692542]	benign	6	35944510	35944515	Human		name
15145426	CV710478	single nucleotide variant	NM_052961.4(SLC26A8):c.60A>G (p.Ser20=)	not provided [RCV000966994]	benign	6	36019648	36019648	Human		name
155996019	CV2398487	single nucleotide variant	NM_052961.4(SLC26A8):c.22G>A (p.Ala8Thr)	not specified [RCV004237810]	uncertain significance	6	36019686	36019686	Human		name
405272289	CV3199308	single nucleotide variant	NM_052961.4(SLC26A8):c.285C>T (p.Asp95=)	SLC26A8-related disorder [RCV003914258]	likely benign	6	36012276	36012276	Human		name , trait , alternate_id
597755089	CV3606545	single nucleotide variant	NM_052961.4(SLC26A8):c.21C>G (p.Ser7Arg)	not specified [RCV004868058]	uncertain significance	6	36019687	36019687	Human		name
401920612	CV2822983	single nucleotide variant	NM_052961.4(SLC26A8):c.378C>T (p.Ile126=)	SLC26A8-related disorder [RCV003980930]\|not provided [RCV003431824]	likely benign	6	36000059	36000059	Human	1	name , trait , alternate_id
405283600	CV3191788	single nucleotide variant	NM_052961.4(SLC26A8):c.639C>T (p.Gly213=)	SLC26A8-related disorder [RCV003921887]	likely benign	6	35992663	35992663	Human		name , trait , alternate_id
405257864	CV3207926	single nucleotide variant	NM_052961.4(SLC26A8):c.837C>A (p.Thr279=)	SLC26A8-related disorder [RCV003941398]	likely benign	6	35991764	35991764	Human		name , trait , alternate_id
405294207	CV3214649	single nucleotide variant	NM_052961.4(SLC26A8):c.643T>C (p.Leu215=)	SLC26A8-related disorder [RCV003934092]	likely benign	6	35992659	35992659	Human		name , trait , alternate_id
15140406	CV735644	single nucleotide variant	NM_052961.4(SLC26A8):c.555C>T (p.Pro185=)	not provided [RCV000899314]	benign	6	35997810	35997810	Human		name
150473803	CV1234342	single nucleotide variant	NM_052961.4(SLC26A8):c.217G>A (p.Val73Met)	not provided [RCV001651661]	benign	6	36012344	36012344	Human		name
152982082	CV1679042	single nucleotide variant	NM_052961.4(SLC26A8):c.290T>C (p.Leu97Pro)	Spermatogenic failure 3 [RCV002248400]	pathogenic	6	36012271	36012271	Human	1	name
152982084	CV1679044	single nucleotide variant	NM_052961.4(SLC26A8):c.212G>T (p.Arg71Leu)	Spermatogenic failure 3 [RCV002248402]	pathogenic\|uncertain significance	6	36012349	36012349	Human	1	name
156315525	CV2192912	single nucleotide variant	NM_052961.4(SLC26A8):c.212G>A (p.Arg71Gln)	not specified [RCV004069474]	uncertain significance	6	36012349	36012349	Human		name
155904836	CV2349594	single nucleotide variant	NM_052961.4(SLC26A8):c.255G>C (p.Met85Ile)	not specified [RCV004204018]	uncertain significance	6	36012306	36012306	Human		name
405276554	CV3198573	single nucleotide variant	NM_052961.4(SLC26A8):c.2613G>C (p.Gly871=)	SLC26A8-related disorder [RCV003903902]	likely benign	6	35944200	35944200	Human		name , trait , alternate_id
405769370	CV3321889	single nucleotide variant	NM_052961.4(SLC26A8):c.178G>A (p.Val60Ile)	not specified [RCV004456708]	uncertain significance	6	36019530	36019530	Human		name
597700961	CV3606543	single nucleotide variant	NM_052961.4(SLC26A8):c.204G>T (p.Arg68Ser)	not specified [RCV004859925]	uncertain significance	6	36012357	36012357	Human		name
597755103	CV3606551	single nucleotide variant	NM_052961.4(SLC26A8):c.251G>A (p.Cys84Tyr)	not specified [RCV004868062]	uncertain significance	6	36012310	36012310	Human		name
598129883	CV3887307	single nucleotide variant	NM_052961.4(SLC26A8):c.1921C>T (p.Leu641=)	not provided [RCV005245367]	likely benign	6	35955463	35955463	Human		name
617152987	CV4020824	single nucleotide variant	NM_052961.4(SLC26A8):c.2614C>T (p.Leu872=)	not provided [RCV005428577]	likely benign	6	35944199	35944199	Human		name
617153043	CV4021017	single nucleotide variant	NM_052961.4(SLC26A8):c.194C>T (p.Ser65Leu)	not provided [RCV005428770]	likely benign	6	36012367	36012367	Human		name
8611978	CV65571	single nucleotide variant	NM_052961.4(SLC26A8):c.260G>A (p.Arg87Gln)	Spermatogenic failure 3 [RCV000043624]	pathogenic	6	36012301	36012301	Human	1	name
15101356	CV722015	single nucleotide variant	NM_052961.4(SLC26A8):c.1902C>T (p.Pro634=)	not provided [RCV000892270]	benign	6	35955482	35955482	Human		name
150453115	CV1219794	single nucleotide variant	NM_052961.4(SLC26A8):c.442A>G (p.Ile148Val)	not provided [RCV001612175]	benign	6	35999995	35999995	Human		name
150446521	CV1232116	single nucleotide variant	NM_052961.4(SLC26A8):c.689G>A (p.Ser230Asn)	not provided [RCV001646024]	benign	6	35992613	35992613	Human		name
152982083	CV1679043	deletion	NM_052961.4(SLC26A8):c.1664del (p.Ile555fs)	Spermatogenic failure 3 [RCV002248401]	pathogenic	6	35959781	35959781	Human	1	name
153305191	CV1687587	single nucleotide variant	NM_052961.4(SLC26A8):c.827C>T (p.Ala276Val)	not provided [RCV002263408]	uncertain significance	6	35991774	35991774	Human		name
156152649	CV2194333	single nucleotide variant	NM_052961.4(SLC26A8):c.716A>G (p.His239Arg)	not specified [RCV004079445]	uncertain significance	6	35992586	35992586	Human		name
156275523	CV2330678	single nucleotide variant	NM_052961.4(SLC26A8):c.668A>G (p.Tyr223Cys)	not specified [RCV004185749]	uncertain significance	6	35992634	35992634	Human		name
156078526	CV2351120	single nucleotide variant	NM_052961.4(SLC26A8):c.379G>A (p.Ala127Thr)	not specified [RCV004213980]	uncertain significance	6	36000058	36000058	Human		name
401741936	CV2697661	single nucleotide variant	NM_052961.4(SLC26A8):c.904A>C (p.Asn302His)	not specified [RCV004300405]	uncertain significance	6	35991697	35991697	Human		name
401758179	CV2731744	single nucleotide variant	NM_052961.4(SLC26A8):c.532G>A (p.Val178Ile)	not specified [RCV004331843]	likely benign	6	35997833	35997833	Human		name
405769425	CV3321898	single nucleotide variant	NM_052961.4(SLC26A8):c.403G>A (p.Val135Ile)	not specified [RCV004456717]	uncertain significance	6	36000034	36000034	Human		name
405769432	CV3321899	single nucleotide variant	NM_052961.4(SLC26A8):c.772G>A (p.Gly258Ser)	not specified [RCV004456718]	uncertain significance	6	35992530	35992530	Human		name
405769439	CV3321900	single nucleotide variant	NM_052961.4(SLC26A8):c.929T>A (p.Met310Lys)	not specified [RCV004456719]	uncertain significance	6	35991672	35991672	Human		name
597700954	CV3606541	single nucleotide variant	NM_052961.4(SLC26A8):c.401C>T (p.Ser134Leu)	not specified [RCV004859924]	uncertain significance	6	36000036	36000036	Human		name
597700968	CV3606546	single nucleotide variant	NM_052961.4(SLC26A8):c.313G>C (p.Val105Leu)	not specified [RCV004859926]	uncertain significance	6	36012248	36012248	Human		name
598169470	CV3918356	single nucleotide variant	NM_052961.4(SLC26A8):c.955A>C (p.Thr319Pro)	not specified [RCV005284284]	uncertain significance	6	35982191	35982191	Human		name
598169491	CV3918361	single nucleotide variant	NM_052961.4(SLC26A8):c.943A>G (p.Ile315Val)	not specified [RCV005284289]	uncertain significance	6	35982203	35982203	Human		name
598177812	CV4008348	single nucleotide variant	NM_052961.4(SLC26A8):c.905A>G (p.Asn302Ser)	Spermatogenic failure 3 [RCV005393867]	uncertain significance	6	35991696	35991696	Human	1	name
150504880	CV1222754	single nucleotide variant	NM_052961.4(SLC26A8):c.1915A>G (p.Ile639Val)	not provided [RCV001621688]	benign	6	35955469	35955469	Human		name
155643501	CV1707878	single nucleotide variant	NM_052961.4(SLC26A8):c.2031T>G (p.Tyr677Ter)	Spermatogenic failure 3 [RCV002289339]	uncertain significance	6	35955353	35955353	Human	1	name
156059721	CV2263002	single nucleotide variant	NM_052961.4(SLC26A8):c.2820G>C (p.Gln940His)	not specified [RCV004131264]	uncertain significance	6	35943993	35943993	Human		name
156145066	CV2265023	single nucleotide variant	NM_052961.4(SLC26A8):c.2200G>C (p.Val734Leu)	not specified [RCV004126183]	uncertain significance	6	35955184	35955184	Human		name
155984801	CV2274740	single nucleotide variant	NM_052961.4(SLC26A8):c.2547G>T (p.Lys849Asn)	not specified [RCV004139101]	uncertain significance	6	35944266	35944266	Human		name
156267051	CV2275522	single nucleotide variant	NM_052961.4(SLC26A8):c.2159G>A (p.Ser720Asn)	not specified [RCV004137169]	uncertain significance	6	35955225	35955225	Human		name
156039456	CV2279028	single nucleotide variant	NM_052961.4(SLC26A8):c.1951A>G (p.Asn651Asp)	not specified [RCV004145712]	uncertain significance	6	35955433	35955433	Human		name
156264589	CV2282673	single nucleotide variant	NM_052961.4(SLC26A8):c.2051G>C (p.Trp684Ser)	not specified [RCV004135222]	uncertain significance	6	35955333	35955333	Human		name
156242981	CV2283234	single nucleotide variant	NM_052961.4(SLC26A8):c.2639G>A (p.Arg880Gln)	not specified [RCV004145906]	likely benign	6	35944174	35944174	Human		name
155997101	CV2288584	single nucleotide variant	NM_052961.4(SLC26A8):c.1559G>A (p.Arg520His)	not specified [RCV004152104]	uncertain significance	6	35961002	35961002	Human		name
156272424	CV2297168	single nucleotide variant	NM_052961.4(SLC26A8):c.2488T>C (p.Tyr830His)	not specified [RCV004151060]	likely benign	6	35944325	35944325	Human		name
156176394	CV2299834	single nucleotide variant	NM_052961.4(SLC26A8):c.2495T>C (p.Met832Thr)	not specified [RCV004148984]	uncertain significance	6	35944318	35944318	Human		name
155996473	CV2398545	single nucleotide variant	NM_052961.4(SLC26A8):c.1808G>A (p.Gly603Glu)	not specified [RCV004237865]	likely benign	6	35959515	35959515	Human		name
329358382	CV2425238	single nucleotide variant	NM_052961.4(SLC26A8):c.1163A>G (p.Asn388Ser)	not specified [RCV004250910]	uncertain significance	6	35977214	35977214	Human		name
329373424	CV2434245	single nucleotide variant	NM_052961.4(SLC26A8):c.2801C>T (p.Pro934Leu)	not specified [RCV004251921]	uncertain significance	6	35944012	35944012	Human		name
329373593	CV2434544	single nucleotide variant	NM_052961.4(SLC26A8):c.2374G>A (p.Val792Met)	not specified [RCV004254246]	uncertain significance	6	35951261	35951261	Human		name
329395350	CV2458290	single nucleotide variant	NM_052961.4(SLC26A8):c.1117A>G (p.Ile373Val)	not specified [RCV004265937]	uncertain significance	6	35977260	35977260	Human		name
401719330	CV2679498	single nucleotide variant	NM_052961.4(SLC26A8):c.2254G>A (p.Ala752Thr)	not specified [RCV004287802]	uncertain significance	6	35951478	35951478	Human		name
401746262	CV2694823	single nucleotide variant	NM_052961.4(SLC26A8):c.1015A>T (p.Ile339Phe)	not specified [RCV004300900]	uncertain significance	6	35982131	35982131	Human		name
401744848	CV2697085	single nucleotide variant	NM_052961.4(SLC26A8):c.1672T>A (p.Cys558Ser)	not specified [RCV004293064]	uncertain significance	6	35959773	35959773	Human		name
401763976	CV2700310	single nucleotide variant	NM_052961.4(SLC26A8):c.1906G>A (p.Ala636Thr)	not specified [RCV004310971]	uncertain significance	6	35955478	35955478	Human		name
401752650	CV2707080	single nucleotide variant	NM_052961.4(SLC26A8):c.1363A>G (p.Asn455Asp)	not specified [RCV004321664]	uncertain significance	6	35968879	35968879	Human		name
401779198	CV2733220	single nucleotide variant	NM_052961.4(SLC26A8):c.1853C>T (p.Pro618Leu)	not specified [RCV004332137]	uncertain significance	6	35959470	35959470	Human		name
401873875	CV2772770	single nucleotide variant	NM_052961.4(SLC26A8):c.2032G>A (p.Glu678Lys)	not specified [RCV004357569]	uncertain significance	6	35955352	35955352	Human		name
401875823	CV2777547	single nucleotide variant	NM_052961.4(SLC26A8):c.1484C>T (p.Ser495Leu)	not specified [RCV004343405]	likely benign	6	35961077	35961077	Human		name
401920610	CV2822982	single nucleotide variant	NM_052961.4(SLC26A8):c.2734C>T (p.Pro912Ser)	not provided [RCV003431823]	benign	6	35944079	35944079	Human		name
405259656	CV3186365	single nucleotide variant	NM_052961.4(SLC26A8):c.1204G>A (p.Val402Ile)	not provided [RCV003884124]\|not specified [RCV004858010]	likely benign\|uncertain significance	6	35975458	35975458	Human		name
405258428	CV3203786	single nucleotide variant	NM_052961.4(SLC26A8):c.2200G>A (p.Val734Met)	SLC26A8-related disorder [RCV003941961]	likely benign	6	35955184	35955184	Human		name , trait , alternate_id
405769355	CV3321886	single nucleotide variant	NM_052961.4(SLC26A8):c.1417A>G (p.Ile473Val)	not specified [RCV004456705]	uncertain significance	6	35962570	35962570	Human		name
405769360	CV3321887	single nucleotide variant	NM_052961.4(SLC26A8):c.1547T>G (p.Ile516Ser)	not specified [RCV004456706]	uncertain significance	6	35961014	35961014	Human		name
405769366	CV3321888	single nucleotide variant	NM_052961.4(SLC26A8):c.1641C>G (p.Ile547Met)	not specified [RCV004456707]	uncertain significance	6	35959804	35959804	Human		name
405769377	CV3321890	single nucleotide variant	NM_052961.4(SLC26A8):c.1810G>A (p.Gly604Arg)	not specified [RCV004456709]	uncertain significance	6	35959513	35959513	Human		name
405769383	CV3321891	single nucleotide variant	NM_052961.4(SLC26A8):c.2028G>C (p.Gln676His)	not specified [RCV004456710]	uncertain significance	6	35955356	35955356	Human		name
405769389	CV3321892	single nucleotide variant	NM_052961.4(SLC26A8):c.2087G>A (p.Gly696Glu)	not specified [RCV004456711]	uncertain significance	6	35955297	35955297	Human		name
405769396	CV3321893	single nucleotide variant	NM_052961.4(SLC26A8):c.2243C>G (p.Ala748Gly)	not specified [RCV004456712]	uncertain significance	6	35951489	35951489	Human		name
405769402	CV3321894	single nucleotide variant	NM_052961.4(SLC26A8):c.2518C>A (p.Gln840Lys)	not specified [RCV004456713]	uncertain significance	6	35944295	35944295	Human		name
405769408	CV3321895	single nucleotide variant	NM_052961.4(SLC26A8):c.2681C>T (p.Thr894Ile)	not specified [RCV004456714]	uncertain significance	6	35944132	35944132	Human		name
405769414	CV3321896	single nucleotide variant	NM_052961.4(SLC26A8):c.2830C>A (p.Gln944Lys)	not specified [RCV004456715]	uncertain significance	6	35943983	35943983	Human		name
407509646	CV3474097	single nucleotide variant	NM_052961.4(SLC26A8):c.2446C>T (p.Arg816Trp)	not specified [RCV004672401]	uncertain significance	6	35951189	35951189	Human		name
407509643	CV3474098	single nucleotide variant	NM_052961.4(SLC26A8):c.2206T>C (p.Ser736Pro)	not specified [RCV004672402]	uncertain significance	6	35955178	35955178	Human		name
407509641	CV3474099	single nucleotide variant	NM_052961.4(SLC26A8):c.1078C>A (p.Gln360Lys)	not specified [RCV004672403]	uncertain significance	6	35977299	35977299	Human		name
597755076	CV3606540	single nucleotide variant	NM_052961.4(SLC26A8):c.2836C>T (p.Arg946Trp)	not specified [RCV004868055]	uncertain significance	6	35943977	35943977	Human		name
597755084	CV3606544	single nucleotide variant	NM_052961.4(SLC26A8):c.2542A>G (p.Ile848Val)	not specified [RCV004868057]	uncertain significance	6	35944271	35944271	Human		name
597755091	CV3606547	single nucleotide variant	NM_052961.4(SLC26A8):c.1079A>G (p.Gln360Arg)	not specified [RCV004868059]	uncertain significance	6	35977298	35977298	Human		name
597755096	CV3606548	single nucleotide variant	NM_052961.4(SLC26A8):c.1913C>G (p.Ser638Cys)	not specified [RCV004868060]	uncertain significance	6	35955471	35955471	Human		name
597700973	CV3606549	single nucleotide variant	NM_052961.4(SLC26A8):c.1948A>G (p.Met650Val)	not specified [RCV004859927]	likely benign	6	35955436	35955436	Human		name
597755108	CV3606552	single nucleotide variant	NM_052961.4(SLC26A8):c.1897G>T (p.Asp633Tyr)	not specified [RCV004868063]	uncertain significance	6	35955487	35955487	Human		name
598169439	CV3918346	single nucleotide variant	NM_052961.4(SLC26A8):c.1740G>T (p.Met580Ile)	not specified [RCV005284276]	uncertain significance	6	35959583	35959583	Human		name
598169443	CV3918347	single nucleotide variant	NM_052961.4(SLC26A8):c.2550C>G (p.Ile850Met)	not specified [RCV005284277]	uncertain significance	6	35944263	35944263	Human		name
598169449	CV3918349	single nucleotide variant	NM_052961.4(SLC26A8):c.1409T>C (p.Leu470Pro)	not specified [RCV005284279]	uncertain significance	6	35962578	35962578	Human		name
598169454	CV3918350	single nucleotide variant	NM_052961.4(SLC26A8):c.2410T>C (p.Ser804Pro)	not specified [RCV005284280]	uncertain significance	6	35951225	35951225	Human		name
598169458	CV3918351	single nucleotide variant	NM_052961.4(SLC26A8):c.1390A>C (p.Ser464Arg)	not specified [RCV005284281]	uncertain significance	6	35962597	35962597	Human		name
598169462	CV3918352	single nucleotide variant	NM_052961.4(SLC26A8):c.2279G>C (p.Gly760Ala)	not specified [RCV005284282]	uncertain significance	6	35951453	35951453	Human		name
598236946	CV3918353	single nucleotide variant	NM_052961.4(SLC26A8):c.2236T>C (p.Cys746Arg)	not specified [RCV005275553]	uncertain significance	6	35951496	35951496	Human		name
598236950	CV3918354	single nucleotide variant	NM_052961.4(SLC26A8):c.1001C>T (p.Thr334Met)	not specified [RCV005275554]	likely benign	6	35982145	35982145	Human		name
598169466	CV3918355	single nucleotide variant	NM_052961.4(SLC26A8):c.2626C>G (p.Leu876Val)	not specified [RCV005284283]	uncertain significance	6	35944187	35944187	Human		name
598169474	CV3918357	single nucleotide variant	NM_052961.4(SLC26A8):c.1408C>T (p.Leu470Phe)	not specified [RCV005284285]	uncertain significance	6	35962579	35962579	Human		name
598169478	CV3918358	single nucleotide variant	NM_052961.4(SLC26A8):c.2780G>A (p.Arg927His)	not specified [RCV005284286]	likely benign	6	35944033	35944033	Human		name
598169487	CV3918360	single nucleotide variant	NM_052961.4(SLC26A8):c.1948A>C (p.Met650Leu)	not specified [RCV005284288]	uncertain significance	6	35955436	35955436	Human		name
598169497	CV3918362	single nucleotide variant	NM_052961.4(SLC26A8):c.2666A>G (p.Lys889Arg)	not specified [RCV005284290]	uncertain significance	6	35944147	35944147	Human		name
598169501	CV3918363	single nucleotide variant	NM_052961.4(SLC26A8):c.1478C>T (p.Thr493Ile)	not specified [RCV005284291]	uncertain significance	6	35961083	35961083	Human		name
598177806	CV4008347	single nucleotide variant	NM_052961.4(SLC26A8):c.1826G>T (p.Cys609Phe)	Spermatogenic failure 3 [RCV005393866]	uncertain significance	6	35959497	35959497	Human	1	name
8611979	CV65572	single nucleotide variant	NM_052961.4(SLC26A8):c.2434G>A (p.Glu812Lys)	Spermatogenic failure 3 [RCV000043625]\|not provided [RCV002513638]\|not specified [RCV002247429]	pathogenic\|likely benign\|uncertain significance	6	35951201	35951201	Human	1	name
8611980	CV65573	single nucleotide variant	NM_052961.4(SLC26A8):c.2860C>T (p.Arg954Cys)	Spermatogenic failure 3 [RCV000043626]	pathogenic\|uncertain significance	6	35943953	35943953	Human	1	name
15167263	CV710475	single nucleotide variant	NM_052961.4(SLC26A8):c.2447G>A (p.Arg816Gln)	not provided [RCV000971363]	benign	6	35951188	35951188	Human		name
15181960	CV710476	single nucleotide variant	NM_052961.4(SLC26A8):c.2425G>A (p.Asp809Asn)	not provided [RCV000974518]	benign	6	35951210	35951210	Human		name
15165580	CV710477	single nucleotide variant	NM_052961.4(SLC26A8):c.1733T>C (p.Val578Ala)	not provided [RCV000970981]	benign	6	35959590	35959590	Human		name
15172312	CV722016	single nucleotide variant	NM_052961.4(SLC26A8):c.1492A>G (p.Ile498Val)	SLC26A8-related disorder [RCV003955869]\|not provided [RCV000883816]	benign\|likely benign	6	35961069	35961069	Human	1	name , trait , alternate_id
15172714	CV735643	single nucleotide variant	NM_052961.4(SLC26A8):c.2894A>G (p.Asn965Ser)	SLC26A8-related disorder [RCV003923067]\|not provided [RCV000905722]	likely benign	6	35943919	35943919	Human	1	name , trait , alternate_id
126730093	CV985971	single nucleotide variant	NM_052961.4(SLC26A8):c.1444C>T (p.Gln482Ter)	Spermatogenic failure 3 [RCV001294049]	pathogenic	6	35962543	35962543	Human		name
8632032	CV87238	single nucleotide variant	NM_001193476.1(SLC26A8):c.2211G>A (p.Arg737=)	Malignant melanoma [RCV000067329]	not provided	6	35955173	35955173	Human		name

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