Slc43a1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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64 records found for search term Slc43a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155901339	CV2294444	single nucleotide variant	NM_003627.6(SLC43A1):c.11C>T (p.Thr4Met)	not specified [RCV004159947]	uncertain significance	11	57514101	57514101	Human		name
156288945	CV2333028	single nucleotide variant	NM_003627.6(SLC43A1):c.11C>A (p.Thr4Lys)	not specified [RCV004194327]	uncertain significance	11	57514101	57514101	Human		name
156187917	CV2395324	single nucleotide variant	NM_003627.6(SLC43A1):c.10A>C (p.Thr4Pro)	not specified [RCV004239420]	uncertain significance	11	57514102	57514102	Human		name
156106341	CV2217823	single nucleotide variant	NM_003627.6(SLC43A1):c.28C>T (p.Arg10Trp)	not specified [RCV004083997]	uncertain significance	11	57514084	57514084	Human		name
156065628	CV2348858	single nucleotide variant	NM_003627.6(SLC43A1):c.44T>A (p.Met15Lys)	not specified [RCV004203298]	uncertain significance	11	57514068	57514068	Human		name
401943261	CV2839986	single nucleotide variant	NM_003627.6(SLC43A1):c.567C>T (p.Tyr189=)	not provided [RCV003456773]	likely benign	11	57496156	57496156	Human		name
405710133	CV3329270	single nucleotide variant	NM_003627.6(SLC43A1):c.50G>C (p.Cys17Ser)	not specified [RCV004461659]	uncertain significance	11	57514062	57514062	Human		name
598237314	CV3911192	single nucleotide variant	NM_003627.6(SLC43A1):c.39G>C (p.Trp13Cys)	not specified [RCV005275632]	uncertain significance	11	57514073	57514073	Human		name
15117073	CV712884	single nucleotide variant	NM_003627.6(SLC43A1):c.543G>A (p.Thr181=)	not provided [RCV000962141]	benign	11	57497768	57497768	Human		name
156048123	CV2390987	single nucleotide variant	NM_003627.6(SLC43A1):c.256G>A (p.Val86Met)	not specified [RCV004234987]	uncertain significance	11	57501228	57501228	Human		name
401883447	CV2785662	single nucleotide variant	NM_003627.6(SLC43A1):c.149G>A (p.Cys50Tyr)	not specified [RCV004364931]	uncertain significance	11	57513963	57513963	Human		name
405710082	CV3329264	single nucleotide variant	NM_003627.6(SLC43A1):c.119T>A (p.Leu40Gln)	not specified [RCV004461653]	uncertain significance	11	57513993	57513993	Human		name
405710115	CV3329268	single nucleotide variant	NM_003627.6(SLC43A1):c.210C>G (p.Asp70Glu)	not specified [RCV004461657]	uncertain significance	11	57501274	57501274	Human		name
407451749	CV3484653	single nucleotide variant	NM_003627.6(SLC43A1):c.200C>G (p.Pro67Arg)	not specified [RCV004683755]	uncertain significance	11	57501284	57501284	Human		name
407514877	CV3484654	single nucleotide variant	NM_003627.6(SLC43A1):c.189G>T (p.Gln63His)	not specified [RCV004674731]	uncertain significance	11	57501295	57501295	Human		name
598237308	CV3911190	single nucleotide variant	NM_003627.6(SLC43A1):c.286A>T (p.Ile96Phe)	not specified [RCV005275631]	uncertain significance	11	57501198	57501198	Human		name
15161027	CV724488	single nucleotide variant	NM_003627.6(SLC43A1):c.118C>A (p.Leu40Met)	not provided [RCV000881495]	benign	11	57513994	57513994	Human		name
156235718	CV2245455	single nucleotide variant	NM_003627.6(SLC43A1):c.811G>A (p.Gly271Ser)	not specified [RCV004109235]	uncertain significance	11	57494053	57494053	Human		name
156143928	CV2268828	single nucleotide variant	NM_003627.6(SLC43A1):c.319C>T (p.Arg107Trp)	not specified [RCV004124205]	uncertain significance	11	57501165	57501165	Human		name
155909458	CV2307282	single nucleotide variant	NM_003627.6(SLC43A1):c.487C>G (p.Leu163Val)	not specified [RCV004159736]	uncertain significance	11	57497824	57497824	Human		name
155919528	CV2360295	single nucleotide variant	NM_003627.6(SLC43A1):c.844C>T (p.Arg282Trp)	not specified [RCV004208636]	uncertain significance	11	57494020	57494020	Human		name
156088917	CV2392012	single nucleotide variant	NM_003627.6(SLC43A1):c.655A>G (p.Ile219Val)	not specified [RCV004235868]	likely benign	11	57496068	57496068	Human		name
329382395	CV2424454	single nucleotide variant	NM_003627.6(SLC43A1):c.817G>A (p.Asp273Asn)	not specified [RCV004252346]	uncertain significance	11	57494047	57494047	Human		name
329385957	CV2458642	single nucleotide variant	NM_003627.6(SLC43A1):c.925C>T (p.Leu309Phe)	not specified [RCV004268314]	uncertain significance	11	57491809	57491809	Human		name
401742204	CV2676917	single nucleotide variant	NM_003627.6(SLC43A1):c.511A>G (p.Met171Val)	not specified [RCV004291077]	uncertain significance	11	57497800	57497800	Human		name
401721834	CV2680696	single nucleotide variant	NM_003627.6(SLC43A1):c.490C>T (p.Arg164Cys)	not specified [RCV004291309]	uncertain significance	11	57497821	57497821	Human		name
401780882	CV2681804	single nucleotide variant	NM_003627.6(SLC43A1):c.298C>T (p.Arg100Cys)	not specified [RCV004296806]	uncertain significance	11	57501186	57501186	Human		name
401772758	CV2687804	single nucleotide variant	NM_003627.6(SLC43A1):c.494C>T (p.Ser165Phe)	not specified [RCV004302784]	uncertain significance	11	57497817	57497817	Human		name
401872369	CV2754350	single nucleotide variant	NM_003627.6(SLC43A1):c.877G>C (p.Val293Leu)	not specified [RCV004334526]	uncertain significance	11	57491857	57491857	Human		name
401872333	CV2793072	single nucleotide variant	NM_003627.6(SLC43A1):c.905C>G (p.Pro302Arg)	not specified [RCV004360398]	uncertain significance	11	57491829	57491829	Human		name
405710124	CV3329269	single nucleotide variant	NM_003627.6(SLC43A1):c.398C>T (p.Pro133Leu)	not specified [RCV004461658]	uncertain significance	11	57500846	57500846	Human		name
405710139	CV3329271	single nucleotide variant	NM_003627.6(SLC43A1):c.680A>G (p.Glu227Gly)	not specified [RCV004461660]	uncertain significance	11	57496043	57496043	Human		name
405710147	CV3329272	single nucleotide variant	NM_003627.6(SLC43A1):c.886C>G (p.Arg296Gly)	not specified [RCV004461661]	uncertain significance	11	57491848	57491848	Human		name
407451752	CV3484657	single nucleotide variant	NM_003627.6(SLC43A1):c.772G>T (p.Gly258Cys)	not specified [RCV004683756]	uncertain significance	11	57494092	57494092	Human		name
407514886	CV3484658	single nucleotide variant	NM_003627.6(SLC43A1):c.449C>A (p.Thr150Lys)	not specified [RCV004674734]	uncertain significance	11	57500795	57500795	Human		name
597766187	CV3600087	single nucleotide variant	NM_003627.6(SLC43A1):c.376C>T (p.Arg126Trp)	not specified [RCV004870571]	uncertain significance	11	57501000	57501000	Human		name
597723292	CV3600088	single nucleotide variant	NM_003627.6(SLC43A1):c.662C>G (p.Ala221Gly)	not specified [RCV004862223]	uncertain significance	11	57496061	57496061	Human		name
597766195	CV3600091	single nucleotide variant	NM_003627.6(SLC43A1):c.443G>T (p.Cys148Phe)	not specified [RCV004870573]	uncertain significance	11	57500801	57500801	Human		name
598244301	CV3911188	single nucleotide variant	NM_003627.6(SLC43A1):c.331A>T (p.Ser111Cys)	not specified [RCV005276839]	uncertain significance	11	57501153	57501153	Human		name
598244316	CV3911191	single nucleotide variant	NM_003627.6(SLC43A1):c.911T>G (p.Phe304Cys)	not specified [RCV005276841]	uncertain significance	11	57491823	57491823	Human		name
15172819	CV712885	single nucleotide variant	NM_003627.6(SLC43A1):c.356C>T (p.Thr119Ile)	not provided [RCV000972487]	benign	11	57501020	57501020	Human		name
156366349	CV2203310	single nucleotide variant	NM_003627.6(SLC43A1):c.1456A>G (p.Ile486Val)	not specified [RCV004071341]	uncertain significance	11	57487172	57487172	Human		name
156292744	CV2233481	single nucleotide variant	NM_003627.6(SLC43A1):c.1400A>G (p.Tyr467Cys)	not specified [RCV004106101]	uncertain significance	11	57488925	57488925	Human		name
156014854	CV2301605	single nucleotide variant	NM_003627.6(SLC43A1):c.1643C>T (p.Pro548Leu)	not specified [RCV004162511]	uncertain significance	11	57485133	57485133	Human		name
156291146	CV2324974	single nucleotide variant	NM_003627.6(SLC43A1):c.1433C>T (p.Thr478Met)	not specified [RCV004175225]	uncertain significance	11	57487195	57487195	Human		name
156363342	CV2329835	single nucleotide variant	NM_003627.6(SLC43A1):c.1139G>A (p.Arg380Gln)	not specified [RCV004183296]	uncertain significance	11	57491278	57491278	Human		name
156171253	CV2400662	single nucleotide variant	NM_003627.6(SLC43A1):c.1485G>T (p.Gln495His)	not specified [RCV004242344]	uncertain significance	11	57487143	57487143	Human		name
401780455	CV2674032	single nucleotide variant	NM_003627.6(SLC43A1):c.1199G>A (p.Gly400Glu)	not specified [RCV004293397]	uncertain significance	11	57489387	57489387	Human		name
401772994	CV2709062	single nucleotide variant	NM_003627.6(SLC43A1):c.1135T>G (p.Trp379Gly)	not specified [RCV004314403]	uncertain significance	11	57491282	57491282	Human		name
401757494	CV2735051	single nucleotide variant	NM_003627.6(SLC43A1):c.1606C>T (p.Arg536Trp)	not specified [RCV004333750]	uncertain significance	11	57485170	57485170	Human		name
401898279	CV2791161	single nucleotide variant	NM_003627.6(SLC43A1):c.1498G>A (p.Ala500Thr)	not specified [RCV004356520]	uncertain significance	11	57487130	57487130	Human		name
405710093	CV3329265	single nucleotide variant	NM_003627.6(SLC43A1):c.1226G>A (p.Arg409His)	not specified [RCV004461654]	uncertain significance	11	57489360	57489360	Human		name
405710102	CV3329266	single nucleotide variant	NM_003627.6(SLC43A1):c.1552C>G (p.Leu518Val)	not specified [RCV004461655]	uncertain significance	11	57485224	57485224	Human		name
405710109	CV3329267	single nucleotide variant	NM_003627.6(SLC43A1):c.1675G>A (p.Ala559Thr)	not specified [RCV004461656]	uncertain significance	11	57485101	57485101	Human		name
407514880	CV3484655	single nucleotide variant	NM_003627.6(SLC43A1):c.1291G>T (p.Val431Leu)	not specified [RCV004674732]	uncertain significance	11	57489295	57489295	Human		name
407514882	CV3484656	single nucleotide variant	NM_003627.6(SLC43A1):c.1146G>T (p.Lys382Asn)	not specified [RCV004674733]	uncertain significance	11	57491271	57491271	Human		name
597723304	CV3600089	single nucleotide variant	NM_003627.6(SLC43A1):c.1638G>A (p.Met546Ile)	not specified [RCV004862224]	uncertain significance	11	57485138	57485138	Human		name
597766192	CV3600090	single nucleotide variant	NM_003627.6(SLC43A1):c.1131G>A (p.Met377Ile)	not specified [RCV004870572]	uncertain significance	11	57491286	57491286	Human		name
598244307	CV3911189	single nucleotide variant	NM_003627.6(SLC43A1):c.1607G>A (p.Arg536Gln)	not specified [RCV005276840]	uncertain significance	11	57485169	57485169	Human		name
598244323	CV3911193	single nucleotide variant	NM_003627.6(SLC43A1):c.1126A>G (p.Ile376Val)	not specified [RCV005276842]	uncertain significance	11	57491291	57491291	Human		name
598244331	CV3911194	single nucleotide variant	NM_003627.6(SLC43A1):c.1579C>T (p.Pro527Ser)	not specified [RCV005276843]	uncertain significance	11	57485197	57485197	Human		name
598244338	CV3911195	single nucleotide variant	NM_003627.6(SLC43A1):c.1000A>G (p.Thr334Ala)	not specified [RCV005276844]	uncertain significance	11	57491734	57491734	Human		name
15151780	CV712883	single nucleotide variant	NM_003627.6(SLC43A1):c.1159G>A (p.Ala387Thr)	not provided [RCV000968213]	benign	11	57491258	57491258	Human		name
15158740	CV738033	single nucleotide variant	NM_003627.6(SLC43A1):c.1014G>C (p.Glu338Asp)	not provided [RCV000902791]	likely benign	11	57491720	57491720	Human		name

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