Slc12a8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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94 records found for search term Slc12a8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8630581	CV85736	single nucleotide variant	NM_024628.5(SLC12A8):c.737-73G>A	Malignant melanoma [RCV000065819]	not provided	3	125120759	125120759	Human		name
156177662	CV2230415	single nucleotide variant	NM_024628.6(SLC12A8):c.62C>G (p.Ala21Gly)	not specified [RCV004095871]	uncertain significance	3	125190511	125190511	Human		name
405767032	CV3328691	single nucleotide variant	NM_024628.6(SLC12A8):c.77G>T (p.Trp26Leu)	not specified [RCV004456311]	uncertain significance	3	125190496	125190496	Human		name
407502848	CV3477119	single nucleotide variant	NM_024628.6(SLC12A8):c.43G>T (p.Ala15Ser)	not specified [RCV004670081]	uncertain significance	3	125211307	125211307	Human		name
156232246	CV2346096	single nucleotide variant	NM_024628.6(SLC12A8):c.293G>A (p.Arg98His)	not specified [RCV004201560]	likely benign	3	125187334	125187334	Human		name
155932746	CV2364460	single nucleotide variant	NM_024628.6(SLC12A8):c.175T>G (p.Phe59Val)	not specified [RCV004216938]	uncertain significance	3	125190398	125190398	Human		name
155906779	CV2379129	single nucleotide variant	NM_024628.6(SLC12A8):c.100T>A (p.Trp34Arg)	not specified [RCV004235925]	uncertain significance	3	125190473	125190473	Human		name
156135581	CV2379906	single nucleotide variant	NM_024628.6(SLC12A8):c.136T>A (p.Phe46Ile)	not specified [RCV004222055]	uncertain significance	3	125190437	125190437	Human		name
156110152	CV2387598	single nucleotide variant	NM_024628.6(SLC12A8):c.251T>C (p.Val84Ala)	not specified [RCV004234149]	uncertain significance	3	125187376	125187376	Human		name
156001019	CV2391840	single nucleotide variant	NM_024628.6(SLC12A8):c.263C>T (p.Thr88Met)	not specified [RCV004235717]	uncertain significance	3	125187364	125187364	Human		name
407502865	CV3477124	single nucleotide variant	NM_024628.6(SLC12A8):c.259G>A (p.Val87Ile)	not specified [RCV004670086]	likely benign	3	125187368	125187368	Human		name
597740417	CV3599457	single nucleotide variant	NM_024628.6(SLC12A8):c.149T>C (p.Met50Thr)	not specified [RCV004864657]	uncertain significance	3	125190424	125190424	Human		name
156374200	CV2198292	single nucleotide variant	NM_024628.6(SLC12A8):c.325A>G (p.Met109Val)	not specified [RCV004081847]	uncertain significance	3	125187302	125187302	Human		name
156179933	CV2225804	single nucleotide variant	NM_024628.6(SLC12A8):c.316G>T (p.Val106Phe)	not specified [RCV004103211]	uncertain significance	3	125187311	125187311	Human		name
156274190	CV2279701	single nucleotide variant	NM_024628.6(SLC12A8):c.574G>C (p.Val192Leu)	not specified [RCV004144321]	uncertain significance	3	125177791	125177791	Human		name
156198627	CV2293708	single nucleotide variant	NM_024628.6(SLC12A8):c.883C>T (p.Leu295Phe)	not specified [RCV004154997]	uncertain significance	3	125118798	125118798	Human		name
156285930	CV2345624	single nucleotide variant	NM_024628.6(SLC12A8):c.580A>C (p.Thr194Pro)	not specified [RCV004205573]	uncertain significance	3	125177785	125177785	Human		name
155902557	CV2386265	single nucleotide variant	NM_024628.6(SLC12A8):c.335C>T (p.Ser112Leu)	not specified [RCV004228616]	uncertain significance	3	125187292	125187292	Human		name
155999041	CV2396351	single nucleotide variant	NM_024628.6(SLC12A8):c.542G>A (p.Arg181His)	not specified [RCV004242076]	uncertain significance	3	125177823	125177823	Human		name
155997341	CV2398702	single nucleotide variant	NM_024628.6(SLC12A8):c.484G>C (p.Val162Leu)	not specified [RCV004240046]	uncertain significance	3	125177881	125177881	Human		name
329360396	CV2442769	single nucleotide variant	NM_024628.6(SLC12A8):c.362C>A (p.Thr121Asn)	not specified [RCV004251601]	uncertain significance	3	125187265	125187265	Human		name
329359762	CV2446398	single nucleotide variant	NM_024628.6(SLC12A8):c.998G>A (p.Arg333His)	not specified [RCV004249517]	uncertain significance	3	125110250	125110250	Human		name
401780170	CV2725910	single nucleotide variant	NM_024628.6(SLC12A8):c.980G>A (p.Gly327Glu)	not specified [RCV004324285]	uncertain significance	3	125110268	125110268	Human		name
401860779	CV2758625	single nucleotide variant	NM_024628.6(SLC12A8):c.362C>T (p.Thr121Ile)	not specified [RCV004337700]	uncertain significance	3	125187265	125187265	Human		name
401893324	CV2765111	single nucleotide variant	NM_024628.6(SLC12A8):c.488C>T (p.Ala163Val)	not specified [RCV004337606]	uncertain significance	3	125177877	125177877	Human		name
401859939	CV2765213	single nucleotide variant	NM_024628.6(SLC12A8):c.454G>A (p.Gly152Arg)	not specified [RCV004339740]	likely benign	3	125177911	125177911	Human		name
405766995	CV3328685	single nucleotide variant	NM_024628.6(SLC12A8):c.309C>A (p.Ser103Arg)	not specified [RCV004456305]	uncertain significance	3	125187318	125187318	Human		name
405767002	CV3328686	single nucleotide variant	NM_024628.6(SLC12A8):c.310G>A (p.Gly104Ser)	not specified [RCV004456306]	uncertain significance	3	125187317	125187317	Human		name
405767008	CV3328687	single nucleotide variant	NM_024628.6(SLC12A8):c.347G>C (p.Gly116Ala)	not specified [RCV004456307]	uncertain significance	3	125187280	125187280	Human		name
405767013	CV3328688	single nucleotide variant	NM_024628.6(SLC12A8):c.473G>A (p.Arg158Gln)	not specified [RCV004456308]	uncertain significance	3	125177892	125177892	Human		name
405767020	CV3328689	single nucleotide variant	NM_024628.6(SLC12A8):c.686C>T (p.Pro229Leu)	not specified [RCV004456309]	uncertain significance	3	125135719	125135719	Human		name
405767025	CV3328690	single nucleotide variant	NM_024628.6(SLC12A8):c.748G>A (p.Gly250Ser)	not specified [RCV004456310]	uncertain significance	3	125120675	125120675	Human		name
405767037	CV3328692	single nucleotide variant	NM_024628.6(SLC12A8):c.903A>G (p.Ile301Met)	not specified [RCV004456312]	uncertain significance	3	125118778	125118778	Human		name
407502845	CV3477118	single nucleotide variant	NM_024628.6(SLC12A8):c.316G>A (p.Val106Ile)	not specified [RCV004670080]	uncertain significance	3	125187311	125187311	Human		name
407502851	CV3477120	single nucleotide variant	NM_024628.6(SLC12A8):c.353C>T (p.Thr118Met)	not specified [RCV004670082]	uncertain significance	3	125187274	125187274	Human		name
407502855	CV3477121	single nucleotide variant	NM_024628.6(SLC12A8):c.625C>T (p.His209Tyr)	not specified [RCV004670083]	uncertain significance	3	125135780	125135780	Human		name
407502868	CV3477125	single nucleotide variant	NM_024628.6(SLC12A8):c.857T>C (p.Leu286Pro)	not specified [RCV004670087]	uncertain significance	3	125118824	125118824	Human		name
597740411	CV3599456	single nucleotide variant	NM_024628.6(SLC12A8):c.328A>G (p.Ile110Val)	not specified [RCV004864656]	uncertain significance	3	125187299	125187299	Human		name
597740443	CV3599462	single nucleotide variant	NM_024628.6(SLC12A8):c.925G>T (p.Gly309Cys)	not specified [RCV004864662]	uncertain significance	3	125110323	125110323	Human		name
598267856	CV3911134	single nucleotide variant	NM_024628.6(SLC12A8):c.728C>T (p.Ala243Val)	not specified [RCV005281662]	uncertain significance	3	125135677	125135677	Human		name
598267888	CV3921504	single nucleotide variant	NM_024628.6(SLC12A8):c.572C>T (p.Ala191Val)	not specified [RCV005281667]	uncertain significance	3	125177793	125177793	Human		name
598267893	CV3921505	single nucleotide variant	NM_024628.6(SLC12A8):c.872C>T (p.Thr291Ile)	not specified [RCV005281668]	uncertain significance	3	125118809	125118809	Human		name
156105730	CV2217676	single nucleotide variant	NM_024628.6(SLC12A8):c.1949G>A (p.Arg650Gln)	not specified [RCV004083870]	uncertain significance	3	125088343	125088343	Human		name
156330661	CV2224299	single nucleotide variant	NM_024628.6(SLC12A8):c.1697G>A (p.Ser566Asn)	not specified [RCV004096120]	uncertain significance	3	125107489	125107489	Human		name
156065851	CV2240325	single nucleotide variant	NM_024628.6(SLC12A8):c.1850C>A (p.Thr617Asn)	not specified [RCV004112879]	uncertain significance	3	125091510	125091510	Human		name
156002127	CV2257925	single nucleotide variant	NM_024628.6(SLC12A8):c.1291G>A (p.Glu431Lys)	not specified [RCV004129744]	uncertain significance	3	125107895	125107895	Human		name
156069317	CV2270973	single nucleotide variant	NM_024628.6(SLC12A8):c.2048T>A (p.Met683Lys)	not specified [RCV004132002]	uncertain significance	3	125083987	125083987	Human		name
156270566	CV2276631	single nucleotide variant	NM_024628.6(SLC12A8):c.1532C>A (p.Ser511Tyr)	not specified [RCV004146112]	uncertain significance	3	125107654	125107654	Human		name
156131368	CV2279937	single nucleotide variant	NM_024628.6(SLC12A8):c.1342C>A (p.Gln448Lys)	not specified [RCV004146311]	uncertain significance	3	125107844	125107844	Human		name
156253428	CV2284051	single nucleotide variant	NM_024628.6(SLC12A8):c.2006A>T (p.Gln669Leu)	not specified [RCV004144657]	uncertain significance	3	125084029	125084029	Human		name
156346706	CV2305443	single nucleotide variant	NM_024628.6(SLC12A8):c.1346G>A (p.Arg449Lys)	not specified [RCV004165166]	uncertain significance	3	125107840	125107840	Human		name
156147650	CV2321563	single nucleotide variant	NM_024628.6(SLC12A8):c.1789G>A (p.Val597Ile)	not specified [RCV004177805]	uncertain significance	3	125092115	125092115	Human		name
156353420	CV2327534	single nucleotide variant	NM_024628.6(SLC12A8):c.1757C>T (p.Thr586Ile)	not specified [RCV004176839]	uncertain significance	3	125092147	125092147	Human		name
155914557	CV2342029	single nucleotide variant	NM_024628.6(SLC12A8):c.1081G>A (p.Val361Met)	not specified [RCV004184965]	uncertain significance	3	125108105	125108105	Human		name
155938660	CV2365067	single nucleotide variant	NM_024628.6(SLC12A8):c.2018C>T (p.Ala673Val)	not specified [RCV004224223]	uncertain significance	3	125084017	125084017	Human		name
156143230	CV2393550	single nucleotide variant	NM_024628.6(SLC12A8):c.1897C>T (p.Arg633Trp)	not specified [RCV004231368]	uncertain significance	3	125091463	125091463	Human		name
156170765	CV2400611	single nucleotide variant	NM_024628.6(SLC12A8):c.2080G>A (p.Ala694Thr)	not specified [RCV004242299]	uncertain significance	3	125083955	125083955	Human		name
329374920	CV2431094	single nucleotide variant	NM_024628.6(SLC12A8):c.1186G>A (p.Val396Ile)	not specified [RCV004250457]	likely benign	3	125108000	125108000	Human		name
329401790	CV2457421	single nucleotide variant	NM_024628.6(SLC12A8):c.1900G>A (p.Ala634Thr)	not specified [RCV004267247]	likely benign	3	125091460	125091460	Human		name
329379078	CV2460142	single nucleotide variant	NM_024628.6(SLC12A8):c.1606A>G (p.Asn536Asp)	not specified [RCV004273247]	uncertain significance	3	125107580	125107580	Human		name
401754312	CV2685231	single nucleotide variant	NM_024628.6(SLC12A8):c.1627G>A (p.Glu543Lys)	not specified [RCV004289782]	uncertain significance	3	125107559	125107559	Human		name
401725890	CV2687336	single nucleotide variant	NM_024628.6(SLC12A8):c.2044G>C (p.Glu682Gln)	not specified [RCV004298267]	uncertain significance	3	125083991	125083991	Human		name
401772067	CV2687403	single nucleotide variant	NM_024628.6(SLC12A8):c.1763T>C (p.Phe588Ser)	not specified [RCV004300652]	uncertain significance	3	125092141	125092141	Human		name
401762454	CV2696132	single nucleotide variant	NM_024628.6(SLC12A8):c.1734A>T (p.Glu578Asp)	not specified [RCV004310192]	uncertain significance	3	125092170	125092170	Human		name
401770438	CV2711171	single nucleotide variant	NM_024628.6(SLC12A8):c.2093G>C (p.Arg698Pro)	not specified [RCV004310842]	uncertain significance	3	125083942	125083942	Human		name
401779622	CV2714644	single nucleotide variant	NM_024628.6(SLC12A8):c.1522G>A (p.Asp508Asn)	not specified [RCV004320230]	uncertain significance	3	125107664	125107664	Human		name
401886399	CV2771265	single nucleotide variant	NM_024628.6(SLC12A8):c.1688C>T (p.Ser563Leu)	not specified [RCV004346242]	uncertain significance	3	125107498	125107498	Human		name
401888185	CV2788097	single nucleotide variant	NM_024628.6(SLC12A8):c.1563C>G (p.Asp521Glu)	not specified [RCV004352726]	uncertain significance	3	125107623	125107623	Human		name
405766967	CV3328680	single nucleotide variant	NM_024628.6(SLC12A8):c.1012A>G (p.Ile338Val)	not specified [RCV004456300]	uncertain significance	3	125110236	125110236	Human		name
405766971	CV3328681	single nucleotide variant	NM_024628.6(SLC12A8):c.1270G>A (p.Ala424Thr)	not specified [RCV004456301]	uncertain significance	3	125107916	125107916	Human		name
405766983	CV3328683	single nucleotide variant	NM_024628.6(SLC12A8):c.1909G>C (p.Gly637Arg)	not specified [RCV004456303]	uncertain significance	3	125091451	125091451	Human		name
405766989	CV3328684	single nucleotide variant	NM_024628.6(SLC12A8):c.2120G>A (p.Arg707Gln)	not specified [RCV004456304]	uncertain significance	3	125083915	125083915	Human		name
407502837	CV3477116	single nucleotide variant	NM_024628.6(SLC12A8):c.2093G>A (p.Arg698His)	not specified [RCV004670078]	uncertain significance	3	125083942	125083942	Human		name
407502841	CV3477117	single nucleotide variant	NM_024628.6(SLC12A8):c.1144G>A (p.Val382Ile)	not specified [RCV004670079]	likely benign	3	125108042	125108042	Human		name
407502862	CV3477123	single nucleotide variant	NM_024628.6(SLC12A8):c.1153C>T (p.Pro385Ser)	not specified [RCV004670085]	uncertain significance	3	125108033	125108033	Human		name
597740395	CV3599453	single nucleotide variant	NM_024628.6(SLC12A8):c.2119C>T (p.Arg707Trp)	not specified [RCV004864653]	uncertain significance	3	125083916	125083916	Human		name
597740401	CV3599454	single nucleotide variant	NM_024628.6(SLC12A8):c.1879G>A (p.Val627Met)	not specified [RCV004864654]	uncertain significance	3	125091481	125091481	Human		name
597740406	CV3599455	single nucleotide variant	NM_024628.6(SLC12A8):c.1948C>T (p.Arg650Trp)	not specified [RCV004864655]	uncertain significance	3	125088344	125088344	Human		name
597740421	CV3599458	single nucleotide variant	NM_024628.6(SLC12A8):c.1438G>C (p.Gly480Arg)	not specified [RCV004864658]	uncertain significance	3	125107748	125107748	Human		name
597740426	CV3599459	single nucleotide variant	NM_024628.6(SLC12A8):c.1952G>T (p.Trp651Leu)	not specified [RCV004864659]	uncertain significance	3	125088340	125088340	Human		name
597740433	CV3599460	single nucleotide variant	NM_024628.6(SLC12A8):c.1858A>G (p.Asn620Asp)	not specified [RCV004864660]	uncertain significance	3	125091502	125091502	Human		name
597740448	CV3599463	single nucleotide variant	NM_024628.6(SLC12A8):c.1475A>G (p.Lys492Arg)	not specified [RCV004864663]	uncertain significance	3	125107711	125107711	Human		name
597740454	CV3599464	single nucleotide variant	NM_024628.6(SLC12A8):c.2010C>G (p.Ile670Met)	not specified [RCV004864664]	uncertain significance	3	125084025	125084025	Human		name
598267831	CV3911130	single nucleotide variant	NM_024628.6(SLC12A8):c.1573G>A (p.Ala525Thr)	not specified [RCV005281658]	likely benign	3	125107613	125107613	Human		name
598267839	CV3911131	single nucleotide variant	NM_024628.6(SLC12A8):c.1159G>A (p.Val387Ile)	not specified [RCV005281659]	uncertain significance	3	125108027	125108027	Human		name
598267845	CV3911132	single nucleotide variant	NM_024628.6(SLC12A8):c.1282C>G (p.His428Asp)	not specified [RCV005281660]	uncertain significance	3	125107904	125107904	Human		name
598267852	CV3911133	single nucleotide variant	NM_024628.6(SLC12A8):c.1836A>G (p.Ile612Met)	not specified [RCV005281661]	uncertain significance	3	125091524	125091524	Human		name
598267863	CV3921500	single nucleotide variant	NM_024628.6(SLC12A8):c.1266G>C (p.Glu422Asp)	not specified [RCV005281663]	uncertain significance	3	125107920	125107920	Human		name
598267875	CV3921502	single nucleotide variant	NM_024628.6(SLC12A8):c.1782C>A (p.Asn594Lys)	not specified [RCV005281665]	uncertain significance	3	125092122	125092122	Human		name
598267881	CV3921503	single nucleotide variant	NM_024628.6(SLC12A8):c.1903A>C (p.Ser635Arg)	not specified [RCV005281666]	uncertain significance	3	125091457	125091457	Human		name
598199837	CV3921506	single nucleotide variant	NM_024628.6(SLC12A8):c.1076C>T (p.Thr359Ile)	not specified [RCV005268454]	uncertain significance	3	125108110	125108110	Human		name
8625491	CV80614	single nucleotide variant	NM_024628.5(SLC12A8):c.1746G>A (p.Trp582Ter)	Malignant melanoma [RCV000060691]	not provided	3	125092158	125092158	Human		name
8630579	CV85734	single nucleotide variant	NM_024628.5(SLC12A8):c.1810G>A (p.Gly604Arg)	Malignant melanoma [RCV000065817]	not provided	3	125091550	125091550	Human		name
8630580	CV85735	single nucleotide variant	NM_024628.5(SLC12A8):c.1333G>A (p.Gly445Arg)	Malignant melanoma [RCV000065818]	not provided	3	125107853	125107853	Human		name

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