Slc6a16 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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78 records found for search term Slc6a16

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329371355	CV2458091	single nucleotide variant	NM_014037.3(SLC6A16):c.14C>T (p.Ala5Val)	not specified [RCV004271916]	uncertain significance	19	49311334	49311334	Human		name
156119428	CV2275813	single nucleotide variant	NM_014037.3(SLC6A16):c.61G>T (p.Val21Leu)	not specified [RCV004139482]	uncertain significance	19	49311287	49311287	Human		name
156101769	CV2352217	single nucleotide variant	NM_014037.3(SLC6A16):c.66T>G (p.Ile22Met)	not specified [RCV004200698]	uncertain significance	19	49311282	49311282	Human		name
405730319	CV3325936	single nucleotide variant	NM_014037.3(SLC6A16):c.279G>C (p.Glu93Asp)	not specified [RCV004464250]	uncertain significance	19	49311069	49311069	Human		name
407515533	CV3481029	single nucleotide variant	NM_014037.3(SLC6A16):c.221C>T (p.Ala74Val)	not specified [RCV004674965]	uncertain significance	19	49311127	49311127	Human		name
597776348	CV3606601	single nucleotide variant	NM_014037.3(SLC6A16):c.164G>A (p.Arg55Gln)	not specified [RCV004872779]	uncertain significance	19	49311184	49311184	Human		name
597776357	CV3606604	single nucleotide variant	NM_014037.3(SLC6A16):c.137C>T (p.Thr46Ile)	not specified [RCV004872781]	uncertain significance	19	49311211	49311211	Human		name
597776365	CV3606608	single nucleotide variant	NM_014037.3(SLC6A16):c.235G>T (p.Ala79Ser)	not specified [RCV004872783]	uncertain significance	19	49311113	49311113	Human		name
598259660	CV3911547	single nucleotide variant	NM_014037.3(SLC6A16):c.254C>T (p.Thr85Met)	not specified [RCV005279626]	uncertain significance	19	49311094	49311094	Human		name
8628368	CV83512	single nucleotide variant	NM_014037.2(SLC6A16):c.1849C>T (p.Leu617=)	Malignant melanoma [RCV000063593]	not provided	19	49290697	49290697	Human		name
8628369	CV83513	single nucleotide variant	NM_014037.2(SLC6A16):c.1521C>T (p.Ala507=)	Malignant melanoma [RCV000063594]	not provided	19	49293924	49293924	Human		name
8636930	CV92155	single nucleotide variant	NM_014037.2(SLC6A16):c.1563T>C (p.Ile521=)	Malignant melanoma [RCV000072253]	not provided	19	49293882	49293882	Human		name
155933003	CV2228786	single nucleotide variant	NM_014037.3(SLC6A16):c.509G>A (p.Gly170Asp)	not specified [RCV004095037]	uncertain significance	19	49310417	49310417	Human		name
156087419	CV2258985	single nucleotide variant	NM_014037.3(SLC6A16):c.424G>A (p.Ala142Thr)	not specified [RCV004120258]	uncertain significance	19	49310502	49310502	Human		name
156031924	CV2274972	single nucleotide variant	NM_014037.3(SLC6A16):c.514A>G (p.Met172Val)	not specified [RCV004135018]	uncertain significance	19	49310412	49310412	Human		name
156103587	CV2310774	single nucleotide variant	NM_014037.3(SLC6A16):c.320C>G (p.Ser107Cys)	not specified [RCV004157701]	uncertain significance	19	49311028	49311028	Human		name
156063123	CV2353903	single nucleotide variant	NM_014037.3(SLC6A16):c.307C>T (p.Arg103Cys)	not specified [RCV004201900]	uncertain significance	19	49311041	49311041	Human		name
156250695	CV2359156	single nucleotide variant	NM_014037.3(SLC6A16):c.848T>A (p.Met283Lys)	not specified [RCV004214513]	uncertain significance	19	49309679	49309679	Human		name
156074231	CV2365513	single nucleotide variant	NM_014037.3(SLC6A16):c.602A>G (p.Asn201Ser)	not specified [RCV004211630]	uncertain significance	19	49310138	49310138	Human		name
329382991	CV2434413	single nucleotide variant	NM_014037.3(SLC6A16):c.854A>G (p.Asn285Ser)	not specified [RCV004254127]	uncertain significance	19	49309673	49309673	Human		name
329351629	CV2459203	single nucleotide variant	NM_014037.3(SLC6A16):c.812C>T (p.Pro271Leu)	not specified [RCV004272645]	uncertain significance	19	49309715	49309715	Human		name
329381632	CV2467346	single nucleotide variant	NM_014037.3(SLC6A16):c.852C>G (p.Ile284Met)	not specified [RCV004285137]	uncertain significance	19	49309675	49309675	Human		name
401757682	CV2675453	single nucleotide variant	NM_014037.3(SLC6A16):c.311C>T (p.Pro104Leu)	not specified [RCV004292251]	uncertain significance	19	49311037	49311037	Human		name
401729893	CV2686992	single nucleotide variant	NM_014037.3(SLC6A16):c.732A>G (p.Ile244Met)	not specified [RCV004304322]	likely benign	19	49309795	49309795	Human		name
405730378	CV3322106	single nucleotide variant	NM_014037.3(SLC6A16):c.955A>G (p.Lys319Glu)	not specified [RCV004464258]	uncertain significance	19	49309333	49309333	Human		name
405730386	CV3322107	single nucleotide variant	NM_014037.3(SLC6A16):c.992C>T (p.Ser331Leu)	not specified [RCV004464259]	uncertain significance	19	49309113	49309113	Human		name
405730324	CV3325937	single nucleotide variant	NM_014037.3(SLC6A16):c.374G>T (p.Cys125Phe)	not specified [RCV004464251]	uncertain significance	19	49310974	49310974	Human		name
405730331	CV3325938	single nucleotide variant	NM_014037.3(SLC6A16):c.460G>A (p.Val154Ile)	not specified [RCV004464252]	likely benign	19	49310466	49310466	Human		name
405730342	CV3325939	single nucleotide variant	NM_014037.3(SLC6A16):c.502C>T (p.Arg168Cys)	not specified [RCV004464253]	uncertain significance	19	49310424	49310424	Human		name
405730355	CV3325941	single nucleotide variant	NM_014037.3(SLC6A16):c.721A>G (p.Thr241Ala)	not specified [RCV004464255]	likely benign	19	49309806	49309806	Human		name
405730363	CV3325942	single nucleotide variant	NM_014037.3(SLC6A16):c.738C>G (p.Phe246Leu)	not specified [RCV004464256]	uncertain significance	19	49309789	49309789	Human		name
407451897	CV3481027	single nucleotide variant	NM_014037.3(SLC6A16):c.589G>A (p.Gly197Ser)	not specified [RCV004683840]	uncertain significance	19	49310151	49310151	Human		name
407451901	CV3481030	single nucleotide variant	NM_014037.3(SLC6A16):c.797A>G (p.Tyr266Cys)	not specified [RCV004683841]	uncertain significance	19	49309730	49309730	Human		name
597776344	CV3606600	single nucleotide variant	NM_014037.3(SLC6A16):c.503G>A (p.Arg168His)	not specified [RCV004872778]	uncertain significance	19	49310423	49310423	Human		name
597776369	CV3606609	single nucleotide variant	NM_014037.3(SLC6A16):c.528G>C (p.Lys176Asn)	not specified [RCV004872784]	uncertain significance	19	49310398	49310398	Human		name
597724624	CV3606610	single nucleotide variant	NM_014037.3(SLC6A16):c.469C>G (p.Leu157Val)	not specified [RCV004862346]	likely benign	19	49310457	49310457	Human		name
597776373	CV3606611	single nucleotide variant	NM_014037.3(SLC6A16):c.379T>C (p.Trp127Arg)	not specified [RCV004872785]	uncertain significance	19	49310969	49310969	Human		name
597776377	CV3606612	single nucleotide variant	NM_014037.3(SLC6A16):c.566G>A (p.Ser189Asn)	not specified [RCV004872786]	uncertain significance	19	49310360	49310360	Human		name
598259686	CV3911552	single nucleotide variant	NM_014037.3(SLC6A16):c.490G>A (p.Gly164Ser)	not specified [RCV005279631]	uncertain significance	19	49310436	49310436	Human		name
598237570	CV3911556	single nucleotide variant	NM_014037.3(SLC6A16):c.388G>A (p.Ala130Thr)	not specified [RCV005275679]	likely benign	19	49310960	49310960	Human		name
156045289	CV2215999	single nucleotide variant	NM_014037.3(SLC6A16):c.1996C>A (p.Leu666Ile)	not specified [RCV004097052]	uncertain significance	19	49290338	49290338	Human		name
156056922	CV2243352	single nucleotide variant	NM_014037.3(SLC6A16):c.1426G>A (p.Gly476Ser)	not specified [RCV004112046]	uncertain significance	19	49294019	49294019	Human		name
155960044	CV2252678	single nucleotide variant	NM_014037.3(SLC6A16):c.1556G>T (p.Gly519Val)	not specified [RCV004118539]	uncertain significance	19	49293889	49293889	Human		name
155986744	CV2259396	single nucleotide variant	NM_014037.3(SLC6A16):c.1550T>C (p.Met517Thr)	not specified [RCV004122623]	uncertain significance	19	49293895	49293895	Human		name
156096713	CV2294398	single nucleotide variant	NM_014037.3(SLC6A16):c.2062T>C (p.Phe688Leu)	not specified [RCV004159908]	uncertain significance	19	49290272	49290272	Human		name
156180840	CV2327767	single nucleotide variant	NM_014037.3(SLC6A16):c.1682T>C (p.Phe561Ser)	not specified [RCV004179114]	uncertain significance	19	49293319	49293319	Human		name
156274509	CV2334111	single nucleotide variant	NM_014037.3(SLC6A16):c.1375C>T (p.Arg459Cys)	not specified [RCV004183626]	uncertain significance	19	49294408	49294408	Human		name
155924643	CV2358186	single nucleotide variant	NM_014037.3(SLC6A16):c.1271T>C (p.Leu424Pro)	not specified [RCV004211986]	uncertain significance	19	49294512	49294512	Human		name
156392208	CV2378388	single nucleotide variant	NM_014037.3(SLC6A16):c.2091G>A (p.Met697Ile)	not specified [RCV004226407]	likely benign	19	49290243	49290243	Human		name
156006011	CV2394098	single nucleotide variant	NM_014037.3(SLC6A16):c.1468T>C (p.Phe490Leu)	not specified [RCV004236305]	uncertain significance	19	49293977	49293977	Human		name
156251807	CV2394365	single nucleotide variant	NM_014037.3(SLC6A16):c.1069G>A (p.Val357Ile)	not specified [RCV004238584]	likely benign	19	49309036	49309036	Human		name
401742760	CV2715312	single nucleotide variant	NM_014037.3(SLC6A16):c.1007T>C (p.Met336Thr)	not specified [RCV004324648]	uncertain significance	19	49309098	49309098	Human		name
401885210	CV2770984	single nucleotide variant	NM_014037.3(SLC6A16):c.2077G>A (p.Gly693Arg)	not specified [RCV004344003]	likely benign	19	49290257	49290257	Human		name
401871081	CV2783416	single nucleotide variant	NM_014037.3(SLC6A16):c.2073G>C (p.Lys691Asn)	not specified [RCV004365765]	uncertain significance	19	49290261	49290261	Human		name
405730280	CV3325931	single nucleotide variant	NM_014037.3(SLC6A16):c.1091T>C (p.Met364Thr)	not specified [RCV004464245]	uncertain significance	19	49309014	49309014	Human		name
405730289	CV3325932	single nucleotide variant	NM_014037.3(SLC6A16):c.1327A>G (p.Asn443Asp)	not specified [RCV004464246]	uncertain significance	19	49294456	49294456	Human		name
405730297	CV3325933	single nucleotide variant	NM_014037.3(SLC6A16):c.1328A>G (p.Asn443Ser)	not specified [RCV004464247]	uncertain significance	19	49294455	49294455	Human		name
405730305	CV3325934	single nucleotide variant	NM_014037.3(SLC6A16):c.1958G>A (p.Arg653Gln)	not specified [RCV004464248]	uncertain significance	19	49290376	49290376	Human		name
405730309	CV3325935	single nucleotide variant	NM_014037.3(SLC6A16):c.2044C>T (p.Arg682Cys)	not specified [RCV004464249]	uncertain significance	19	49290290	49290290	Human		name
407451894	CV3481025	single nucleotide variant	NM_014037.3(SLC6A16):c.2090T>G (p.Met697Arg)	not specified [RCV004683839]	uncertain significance	19	49290244	49290244	Human		name
407515527	CV3481026	single nucleotide variant	NM_014037.3(SLC6A16):c.1735G>A (p.Val579Ile)	not specified [RCV004674963]	likely benign	19	49293266	49293266	Human		name
407451904	CV3481031	single nucleotide variant	NM_014037.3(SLC6A16):c.1651C>A (p.Leu551Ile)	not specified [RCV004683842]	uncertain significance	19	49293350	49293350	Human		name
407515536	CV3481032	single nucleotide variant	NM_014037.3(SLC6A16):c.1670C>T (p.Ser557Leu)	not specified [RCV004674966]	uncertain significance	19	49293331	49293331	Human		name
597776341	CV3606599	single nucleotide variant	NM_014037.3(SLC6A16):c.2045G>A (p.Arg682His)	not specified [RCV004872777]	uncertain significance	19	49290289	49290289	Human		name
597776352	CV3606602	single nucleotide variant	NM_014037.3(SLC6A16):c.1796C>A (p.Thr599Lys)	not specified [RCV004872780]	uncertain significance	19	49290750	49290750	Human		name
597724584	CV3606603	single nucleotide variant	NM_014037.3(SLC6A16):c.1970C>T (p.Pro657Leu)	not specified [RCV004862343]	uncertain significance	19	49290364	49290364	Human		name
597776360	CV3606605	single nucleotide variant	NM_014037.3(SLC6A16):c.1354C>T (p.His452Tyr)	not specified [RCV004872782]	uncertain significance	19	49294429	49294429	Human		name
597724598	CV3606606	single nucleotide variant	NM_014037.3(SLC6A16):c.1604C>G (p.Thr535Arg)	not specified [RCV004862344]	uncertain significance	19	49293841	49293841	Human		name
597724610	CV3606607	single nucleotide variant	NM_014037.3(SLC6A16):c.1214A>C (p.His405Pro)	not specified [RCV004862345]	uncertain significance	19	49308891	49308891	Human		name
598259655	CV3911546	single nucleotide variant	NM_014037.3(SLC6A16):c.1523T>C (p.Met508Thr)	not specified [RCV005279625]	uncertain significance	19	49293922	49293922	Human		name
598259666	CV3911548	single nucleotide variant	NM_014037.3(SLC6A16):c.2185C>T (p.Pro729Ser)	not specified [RCV005279627]	uncertain significance	19	49290149	49290149	Human		name
598259671	CV3911549	single nucleotide variant	NM_014037.3(SLC6A16):c.1878T>G (p.Phe626Leu)	not specified [RCV005279628]	uncertain significance	19	49290668	49290668	Human		name
598259676	CV3911550	single nucleotide variant	NM_014037.3(SLC6A16):c.1451T>C (p.Phe484Ser)	not specified [RCV005279629]	uncertain significance	19	49293994	49293994	Human		name
598259681	CV3911551	single nucleotide variant	NM_014037.3(SLC6A16):c.1007T>G (p.Met336Arg)	not specified [RCV005279630]	uncertain significance	19	49309098	49309098	Human		name
598259691	CV3911553	single nucleotide variant	NM_014037.3(SLC6A16):c.1555G>A (p.Gly519Ser)	not specified [RCV005279632]	uncertain significance	19	49293890	49293890	Human		name
598259696	CV3911554	single nucleotide variant	NM_014037.3(SLC6A16):c.1121C>G (p.Ala374Gly)	not specified [RCV005279633]	uncertain significance	19	49308984	49308984	Human		name
598259701	CV3911555	single nucleotide variant	NM_014037.3(SLC6A16):c.2185C>A (p.Pro729Thr)	not specified [RCV005279634]	uncertain significance	19	49290149	49290149	Human		name
8636931	CV92156	single nucleotide variant	NM_014037.2(SLC6A16):c.1076C>T (p.Ser359Phe)	Malignant melanoma [RCV000072254]	not provided	19	49309029	49309029	Human		name

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