Slc22a6 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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58 records found for search term Slc22a6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597699038	CV3596599	single nucleotide variant	NM_153276.3(SLC22A6):c.4G>T (p.Ala2Ser)	not specified [RCV004859702]	uncertain significance	11	62984687	62984687	Human		name
401773829	CV2727646	single nucleotide variant	NM_153276.3(SLC22A6):c.44G>A (p.Arg15His)	not specified [RCV004329826]	uncertain significance	11	62984647	62984647	Human		name
156139470	CV2250493	single nucleotide variant	NM_153276.3(SLC22A6):c.164C>T (p.Ala55Val)	not specified [RCV004127358]	uncertain significance	11	62984527	62984527	Human		name
329376096	CV2437969	single nucleotide variant	NM_153276.3(SLC22A6):c.185G>C (p.Gly62Ala)	not specified [RCV004263685]	uncertain significance	11	62984506	62984506	Human		name
405733547	CV3325316	single nucleotide variant	NM_153276.3(SLC22A6):c.239G>A (p.Arg80His)	not specified [RCV004451340]	uncertain significance	11	62984452	62984452	Human		name
407509106	CV3473894	single nucleotide variant	NM_153276.3(SLC22A6):c.254A>C (p.Gln85Pro)	not specified [RCV004672255]	uncertain significance	11	62984437	62984437	Human		name
407519588	CV3473896	single nucleotide variant	NM_153276.3(SLC22A6):c.206G>A (p.Arg69Gln)	not specified [RCV004676592]	uncertain significance	11	62984485	62984485	Human		name
597699084	CV3596604	single nucleotide variant	NM_153276.3(SLC22A6):c.1488C>T (p.Ala496=)	not specified [RCV004859707]	likely benign	11	62977261	62977261	Human		name
597699130	CV3596609	single nucleotide variant	NM_153276.3(SLC22A6):c.251C>T (p.Pro84Leu)	not specified [RCV004859712]	uncertain significance	11	62984440	62984440	Human		name
15138726	CV712978	single nucleotide variant	NM_153276.3(SLC22A6):c.1470C>T (p.Tyr490=)	not provided [RCV000965839]	benign	11	62977279	62977279	Human		name
156228889	CV2213121	single nucleotide variant	NM_153276.3(SLC22A6):c.319G>A (p.Asp107Asn)	not specified [RCV004091665]	uncertain significance	11	62984372	62984372	Human		name
156036741	CV2218430	single nucleotide variant	NM_153276.3(SLC22A6):c.929G>A (p.Arg310Gln)	not specified [RCV004090720]	likely benign	11	62981093	62981093	Human		name
155989366	CV2244244	single nucleotide variant	NM_153276.3(SLC22A6):c.700C>G (p.Gln234Glu)	not specified [RCV004100242]	uncertain significance	11	62981939	62981939	Human		name
155985330	CV2247855	single nucleotide variant	NM_153276.3(SLC22A6):c.569C>T (p.Ala190Val)	not specified [RCV004121315]	uncertain significance	11	62983596	62983596	Human		name
156061397	CV2320908	single nucleotide variant	NM_153276.3(SLC22A6):c.449T>C (p.Met150Thr)	not specified [RCV004172720]	uncertain significance	11	62983968	62983968	Human		name
156144357	CV2383924	single nucleotide variant	NM_153276.3(SLC22A6):c.893G>A (p.Arg298Gln)	not specified [RCV004231776]	likely benign	11	62981288	62981288	Human		name
329386979	CV2452747	single nucleotide variant	NM_153276.3(SLC22A6):c.664G>A (p.Val222Met)	not specified [RCV004275292]	uncertain significance	11	62981975	62981975	Human		name
329402533	CV2454773	single nucleotide variant	NM_153276.3(SLC22A6):c.858G>T (p.Arg286Ser)	not specified [RCV004270003]	uncertain significance	11	62981323	62981323	Human		name
401758298	CV2704276	single nucleotide variant	NM_153276.3(SLC22A6):c.620T>A (p.Met207Lys)	not specified [RCV004311267]	uncertain significance	11	62983545	62983545	Human		name
401887945	CV2768882	single nucleotide variant	NM_153276.3(SLC22A6):c.785T>C (p.Phe262Ser)	not specified [RCV004346991]	uncertain significance	11	62981854	62981854	Human		name
405733554	CV3325317	single nucleotide variant	NM_153276.3(SLC22A6):c.640A>T (p.Met214Leu)	not specified [RCV004451341]	uncertain significance	11	62981999	62981999	Human		name
407509113	CV3473897	single nucleotide variant	NM_153276.3(SLC22A6):c.485G>A (p.Arg162Gln)	not specified [RCV004672257]	uncertain significance	11	62983680	62983680	Human		name
407509116	CV3473899	single nucleotide variant	NM_153276.3(SLC22A6):c.375C>A (p.Asp125Glu)	not specified [RCV004672258]	uncertain significance	11	62984042	62984042	Human		name
407509119	CV3473900	single nucleotide variant	NM_153276.3(SLC22A6):c.665T>G (p.Val222Gly)	not specified [RCV004672259]	uncertain significance	11	62981974	62981974	Human		name
597699064	CV3596602	single nucleotide variant	NM_153276.3(SLC22A6):c.892C>T (p.Arg298Trp)	not specified [RCV004859705]	uncertain significance	11	62981289	62981289	Human		name
597699072	CV3596603	single nucleotide variant	NM_153276.3(SLC22A6):c.802T>C (p.Phe268Leu)	not specified [RCV004859706]	uncertain significance	11	62981379	62981379	Human		name
597699120	CV3596608	single nucleotide variant	NM_153276.3(SLC22A6):c.584C>T (p.Ser195Leu)	not specified [RCV004859711]	uncertain significance	11	62983581	62983581	Human		name
597699165	CV3596614	single nucleotide variant	NM_153276.3(SLC22A6):c.958G>A (p.Gly320Ser)	not specified [RCV004859717]	uncertain significance	11	62981064	62981064	Human		name
597699174	CV3596615	single nucleotide variant	NM_153276.3(SLC22A6):c.719T>G (p.Val240Gly)	not specified [RCV004859718]	uncertain significance	11	62981920	62981920	Human		name
597699185	CV3596616	single nucleotide variant	NM_153276.3(SLC22A6):c.725A>T (p.Tyr242Phe)	not specified [RCV004859719]	uncertain significance	11	62981914	62981914	Human		name
598200244	CV3918050	single nucleotide variant	NM_153276.3(SLC22A6):c.727G>T (p.Ala243Ser)	not specified [RCV005268512]	uncertain significance	11	62981912	62981912	Human		name
598269831	CV3921929	single nucleotide variant	NM_153276.3(SLC22A6):c.878G>A (p.Arg293Gln)	not specified [RCV005282034]	uncertain significance	11	62981303	62981303	Human		name
8634258	CV89476	single nucleotide variant	NM_004790.4(SLC22A6):c.794C>T (p.Ser265Phe)	Malignant melanoma [RCV000069573]	not provided	11	62981845	62981845	Human		name
156279436	CV2206271	single nucleotide variant	NM_153276.3(SLC22A6):c.1438G>A (p.Glu480Lys)	not specified [RCV004078620]	uncertain significance	11	62977311	62977311	Human		name
155939329	CV2225453	single nucleotide variant	NM_153276.3(SLC22A6):c.1360C>T (p.Arg454Trp)	not specified [RCV004100851]	uncertain significance	11	62979489	62979489	Human		name
155999335	CV2261078	single nucleotide variant	NM_153276.3(SLC22A6):c.1147C>T (p.Leu383Phe)	not specified [RCV004127724]	uncertain significance	11	62979839	62979839	Human		name
401744213	CV2688118	single nucleotide variant	NM_153276.3(SLC22A6):c.1428C>A (p.Ser476Arg)	not specified [RCV004305171]	uncertain significance	11	62977321	62977321	Human		name
401743771	CV2726162	single nucleotide variant	NM_153276.3(SLC22A6):c.1454T>C (p.Met485Thr)	not specified [RCV004326641]	uncertain significance	11	62977295	62977295	Human		name
401895733	CV2771120	single nucleotide variant	NM_153276.3(SLC22A6):c.1099A>C (p.Ile367Leu)	not specified [RCV004346124]	uncertain significance	11	62979887	62979887	Human		name
401898208	CV2790950	single nucleotide variant	NM_153276.3(SLC22A6):c.1431G>A (p.Met477Ile)	not specified [RCV004354581]	uncertain significance	11	62977318	62977318	Human		name
405733522	CV3325313	single nucleotide variant	NM_153276.3(SLC22A6):c.1392G>T (p.Met464Ile)	not specified [RCV004451337]	uncertain significance	11	62977357	62977357	Human		name
405733538	CV3325315	single nucleotide variant	NM_153276.3(SLC22A6):c.1456C>A (p.Pro486Thr)	not specified [RCV004451339]	uncertain significance	11	62977293	62977293	Human		name
407509109	CV3473895	single nucleotide variant	NM_153276.3(SLC22A6):c.1247C>A (p.Pro416His)	not specified [RCV004672256]	uncertain significance	11	62979739	62979739	Human		name
407519590	CV3473898	single nucleotide variant	NM_153276.3(SLC22A6):c.1183C>T (p.Arg395Trp)	not specified [RCV004676593]	uncertain significance	11	62979803	62979803	Human		name
407509123	CV3473902	single nucleotide variant	NM_153276.3(SLC22A6):c.1552G>A (p.Asp518Asn)	not specified [RCV004672260]	uncertain significance	11	62977197	62977197	Human		name
597699046	CV3596600	single nucleotide variant	NM_153276.3(SLC22A6):c.1009C>T (p.His337Tyr)	not specified [RCV004859703]	uncertain significance	11	62981013	62981013	Human		name
597699092	CV3596605	single nucleotide variant	NM_153276.3(SLC22A6):c.1495G>T (p.Ala499Ser)	not specified [RCV004859708]	uncertain significance	11	62977254	62977254	Human		name
597699101	CV3596606	single nucleotide variant	NM_153276.3(SLC22A6):c.1628C>T (p.Ser543Leu)	not specified [RCV004859709]	uncertain significance	11	62976819	62976819	Human		name
597699112	CV3596607	single nucleotide variant	NM_153276.3(SLC22A6):c.1130T>C (p.Val377Ala)	not specified [RCV004859710]	uncertain significance	11	62979856	62979856	Human		name
597699137	CV3596610	single nucleotide variant	NM_153276.3(SLC22A6):c.1082A>C (p.Gln361Pro)	not specified [RCV004859713]	uncertain significance	11	62979904	62979904	Human		name
597699144	CV3596611	single nucleotide variant	NM_153276.3(SLC22A6):c.1408A>G (p.Ile470Val)	not specified [RCV004859714]	uncertain significance	11	62977341	62977341	Human		name
597699157	CV3596613	single nucleotide variant	NM_153276.3(SLC22A6):c.1315A>T (p.Asn439Tyr)	not specified [RCV004859716]	uncertain significance	11	62979534	62979534	Human		name
598269846	CV3918048	single nucleotide variant	NM_153276.3(SLC22A6):c.1184G>C (p.Arg395Pro)	not specified [RCV005282037]	uncertain significance	11	62979802	62979802	Human		name
598269851	CV3918049	single nucleotide variant	NM_153276.3(SLC22A6):c.1069G>C (p.Val357Leu)	not specified [RCV005282038]	uncertain significance	11	62979917	62979917	Human		name
598269856	CV3918051	single nucleotide variant	NM_153276.3(SLC22A6):c.1354A>G (p.Met452Val)	not specified [RCV005282039]	likely benign	11	62979495	62979495	Human		name
598269861	CV3918052	single nucleotide variant	NM_153276.3(SLC22A6):c.1016T>G (p.Phe339Cys)	not specified [RCV005282040]	uncertain significance	11	62981006	62981006	Human		name
598269826	CV3921928	single nucleotide variant	NM_153276.3(SLC22A6):c.1411G>A (p.Val471Met)	not specified [RCV005282033]	uncertain significance	11	62977338	62977338	Human		name
598269836	CV3921930	single nucleotide variant	NM_153276.3(SLC22A6):c.1493G>C (p.Ser498Thr)	not specified [RCV005282035]	uncertain significance	11	62977256	62977256	Human		name

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