Slc27a6 Variant Search Result - Rat Genome Database

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70 records found for search term Slc27a6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8631367	CV86528	single nucleotide variant	NM_001017372.1(SLC27A6):c.147G>A (p.Lys49=)	Malignant melanoma [RCV000066619]	not provided	5	128966284	128966284	Human		name
401717861	CV2704044	single nucleotide variant	NM_001017372.3(SLC27A6):c.47T>G (p.Leu16Arg)	not specified [RCV004308927]	uncertain significance	5	128966184	128966184	Human		name
405770055	CV3321999	single nucleotide variant	NM_001017372.3(SLC27A6):c.44T>C (p.Val15Ala)	not specified [RCV004456818]	uncertain significance	5	128966181	128966181	Human		name
155970515	CV2241436	single nucleotide variant	NM_001017372.3(SLC27A6):c.224A>G (p.Tyr75Cys)	not specified [RCV004104349]	uncertain significance	5	128966361	128966361	Human		name
156240347	CV2286040	single nucleotide variant	NM_001017372.3(SLC27A6):c.128G>A (p.Arg43Gln)	not specified [RCV004143941]	uncertain significance	5	128966265	128966265	Human		name
156362999	CV2330473	single nucleotide variant	NM_001017372.3(SLC27A6):c.130C>G (p.Leu44Val)	not specified [RCV004181042]	uncertain significance	5	128966267	128966267	Human		name
401781496	CV2682017	single nucleotide variant	NM_001017372.3(SLC27A6):c.149G>A (p.Arg50Lys)	not specified [RCV004290084]	likely benign	5	128966286	128966286	Human		name
401895985	CV2776298	single nucleotide variant	NM_001017372.3(SLC27A6):c.112G>A (p.Val38Met)	not specified [RCV004355450]	uncertain significance	5	128966249	128966249	Human		name
405770048	CV3321998	single nucleotide variant	NM_001017372.3(SLC27A6):c.176A>T (p.Lys59Ile)	not specified [RCV004456817]	uncertain significance	5	128966313	128966313	Human		name
597755289	CV3602747	single nucleotide variant	NM_001017372.3(SLC27A6):c.239A>C (p.Tyr80Ser)	not specified [RCV004868111]	uncertain significance	5	128966376	128966376	Human		name
156032799	CV2236059	single nucleotide variant	NM_001017372.3(SLC27A6):c.731G>T (p.Gly244Val)	not specified [RCV004114219]	uncertain significance	5	128988645	128988645	Human		name
155971333	CV2262327	single nucleotide variant	NM_001017372.3(SLC27A6):c.361G>A (p.Val121Met)	not specified [RCV004128520]	uncertain significance	5	128966498	128966498	Human		name
156167642	CV2270501	single nucleotide variant	NM_001017372.3(SLC27A6):c.989A>G (p.His330Arg)	not specified [RCV004137460]	uncertain significance	5	129015904	129015904	Human		name
156266247	CV2312311	single nucleotide variant	NM_001017372.3(SLC27A6):c.491G>C (p.Gly164Ala)	not specified [RCV004167019]	uncertain significance	5	128985142	128985142	Human		name
156402188	CV2368127	single nucleotide variant	NM_001017372.3(SLC27A6):c.658C>T (p.Leu220Phe)	not specified [RCV004216475]	uncertain significance	5	128985309	128985309	Human		name
155929607	CV2369789	single nucleotide variant	NM_001017372.3(SLC27A6):c.619C>T (p.Arg207Cys)	not specified [RCV004215176]	uncertain significance	5	128985270	128985270	Human		name
155934546	CV2372493	single nucleotide variant	NM_001017372.3(SLC27A6):c.817C>G (p.Leu273Val)	not specified [RCV004219290]	uncertain significance	5	128988731	128988731	Human		name
329376720	CV2428520	single nucleotide variant	NM_001017372.3(SLC27A6):c.527A>C (p.Asn176Thr)	not specified [RCV004253306]	uncertain significance	5	128985178	128985178	Human		name
405770061	CV3322000	single nucleotide variant	NM_001017372.3(SLC27A6):c.541G>A (p.Gly181Arg)	not specified [RCV004456819]	uncertain significance	5	128985192	128985192	Human		name
405770065	CV3322001	single nucleotide variant	NM_001017372.3(SLC27A6):c.628C>T (p.His210Tyr)	not specified [RCV004456820]	uncertain significance	5	128985279	128985279	Human		name
405770069	CV3322002	single nucleotide variant	NM_001017372.3(SLC27A6):c.778T>C (p.Tyr260His)	not specified [RCV004456821]	uncertain significance	5	128988692	128988692	Human		name
405770075	CV3322003	single nucleotide variant	NM_001017372.3(SLC27A6):c.985G>A (p.Asp329Asn)	not specified [RCV004456822]	uncertain significance	5	129015900	129015900	Human		name
407451385	CV3474154	single nucleotide variant	NM_001017372.3(SLC27A6):c.758G>C (p.Cys253Ser)	not specified [RCV004683649]	uncertain significance	5	128988672	128988672	Human		name
407509565	CV3474155	single nucleotide variant	NM_001017372.3(SLC27A6):c.344A>G (p.Glu115Gly)	not specified [RCV004672442]	uncertain significance	5	128966481	128966481	Human		name
407509572	CV3474157	single nucleotide variant	NM_001017372.3(SLC27A6):c.410C>G (p.Thr137Ser)	not specified [RCV004672444]	likely benign	5	128966547	128966547	Human		name
407451387	CV3474159	single nucleotide variant	NM_001017372.3(SLC27A6):c.425A>T (p.Asn142Ile)	not specified [RCV004683650]	uncertain significance	5	128966562	128966562	Human		name
597755293	CV3602748	single nucleotide variant	NM_001017372.3(SLC27A6):c.451T>C (p.Cys151Arg)	not specified [RCV004868112]	uncertain significance	5	128966588	128966588	Human		name
597755297	CV3602749	single nucleotide variant	NM_001017372.3(SLC27A6):c.377C>T (p.Ala126Val)	not specified [RCV004868113]	uncertain significance	5	128966514	128966514	Human		name
597755301	CV3602751	single nucleotide variant	NM_001017372.3(SLC27A6):c.409A>G (p.Thr137Ala)	not specified [RCV004868114]	uncertain significance	5	128966546	128966546	Human		name
598169694	CV3918417	single nucleotide variant	NM_001017372.3(SLC27A6):c.494C>T (p.Thr165Met)	not specified [RCV005284338]	uncertain significance	5	128985145	128985145	Human		name
598169700	CV3918419	single nucleotide variant	NM_001017372.3(SLC27A6):c.413A>G (p.Asn138Ser)	not specified [RCV005284340]	uncertain significance	5	128966550	128966550	Human		name
598169706	CV3918421	single nucleotide variant	NM_001017372.3(SLC27A6):c.336G>A (p.Met112Ile)	not specified [RCV005284342]	uncertain significance	5	128966473	128966473	Human		name
598169708	CV3918422	single nucleotide variant	NM_001017372.3(SLC27A6):c.787C>A (p.Leu263Ile)	not specified [RCV005284343]	uncertain significance	5	128988701	128988701	Human		name
598169711	CV3918423	single nucleotide variant	NM_001017372.3(SLC27A6):c.475G>C (p.Gly159Arg)	not specified [RCV005284344]	uncertain significance	5	128966612	128966612	Human		name
8631368	CV86529	single nucleotide variant	NM_001017372.1(SLC27A6):c.604G>A (p.Asp202Asn)	Malignant melanoma [RCV000066620]	not provided	5	128985255	128985255	Human		name
155741627	CV1770441	single nucleotide variant	NM_001017372.3(SLC27A6):c.1531G>T (p.Val511Phe)	Hepatocellular carcinoma [RCV002302665]	pathogenic	5	129028421	129028421	Human	1	name
156387126	CV2221410	single nucleotide variant	NM_001017372.3(SLC27A6):c.1604C>T (p.Ser535Phe)	not specified [RCV004096705]	uncertain significance	5	129029628	129029628	Human		name
156312905	CV2256938	single nucleotide variant	NM_001017372.3(SLC27A6):c.1400T>G (p.Val467Gly)	not specified [RCV004121133]	uncertain significance	5	129027277	129027277	Human		name
156253031	CV2311421	single nucleotide variant	NM_001017372.3(SLC27A6):c.1662T>G (p.Cys554Trp)	not specified [RCV004168268]	uncertain significance	5	129029686	129029686	Human		name
156150594	CV2318672	single nucleotide variant	NM_001017372.3(SLC27A6):c.1514T>G (p.Phe505Cys)	not specified [RCV004173567]	uncertain significance	5	129028404	129028404	Human		name
156302519	CV2319613	single nucleotide variant	NM_001017372.3(SLC27A6):c.1733T>G (p.Val578Gly)	not specified [RCV004185162]	uncertain significance	5	129033155	129033155	Human		name
156219273	CV2344877	single nucleotide variant	NM_001017372.3(SLC27A6):c.1474G>A (p.Ala492Thr)	not specified [RCV004191016]	uncertain significance	5	129028364	129028364	Human		name
156122434	CV2354329	single nucleotide variant	NM_001017372.3(SLC27A6):c.1138A>G (p.Ile380Val)	not specified [RCV004206746]	likely benign	5	129016053	129016053	Human		name
155911326	CV2362428	single nucleotide variant	NM_001017372.3(SLC27A6):c.1009G>A (p.Gly337Arg)	not specified [RCV004213049]	uncertain significance	5	129015924	129015924	Human		name
156150938	CV2377519	single nucleotide variant	NM_001017372.3(SLC27A6):c.1185A>C (p.Leu395Phe)	not specified [RCV004225678]	uncertain significance	5	129023640	129023640	Human		name
156269661	CV2398598	single nucleotide variant	NM_001017372.3(SLC27A6):c.1027G>A (p.Asp343Asn)	not specified [RCV004237908]	uncertain significance	5	129015942	129015942	Human		name
329382477	CV2449014	single nucleotide variant	NM_001017372.3(SLC27A6):c.1700C>A (p.Thr567Lys)	not specified [RCV004264091]	uncertain significance	5	129033122	129033122	Human		name
329376834	CV2460560	single nucleotide variant	NM_001017372.3(SLC27A6):c.1768C>A (p.Pro590Thr)	not specified [RCV004268839]	uncertain significance	5	129033190	129033190	Human		name
401763234	CV2714474	single nucleotide variant	NM_001017372.3(SLC27A6):c.1303T>C (p.Phe435Leu)	not specified [RCV004317997]	uncertain significance	5	129027180	129027180	Human		name
401729638	CV2733205	single nucleotide variant	NM_001017372.3(SLC27A6):c.1603T>A (p.Ser535Thr)	not specified [RCV004332124]	uncertain significance	5	129029627	129029627	Human		name
401890485	CV2768050	single nucleotide variant	NM_001017372.3(SLC27A6):c.1480A>G (p.Thr494Ala)	not specified [RCV004348290]	uncertain significance	5	129028370	129028370	Human		name
401874353	CV2773914	single nucleotide variant	NM_001017372.3(SLC27A6):c.1229A>G (p.Gln410Arg)	not specified [RCV004358343]	uncertain significance	5	129023684	129023684	Human		name
405770040	CV3321997	single nucleotide variant	NM_001017372.3(SLC27A6):c.1745T>G (p.Phe582Cys)	not specified [RCV004456816]	uncertain significance	5	129033167	129033167	Human		name
407451382	CV3474152	single nucleotide variant	NM_001017372.3(SLC27A6):c.1447A>G (p.Thr483Ala)	not specified [RCV004683648]	uncertain significance	5	129027324	129027324	Human		name
407509564	CV3474153	single nucleotide variant	NM_001017372.3(SLC27A6):c.1250A>T (p.Lys417Ile)	not specified [RCV004672441]	uncertain significance	5	129023705	129023705	Human		name
407509569	CV3474156	single nucleotide variant	NM_001017372.3(SLC27A6):c.1553G>T (p.Gly518Val)	not specified [RCV004672443]	uncertain significance	5	129029577	129029577	Human		name
407509575	CV3474158	single nucleotide variant	NM_001017372.3(SLC27A6):c.1444G>T (p.Asp482Tyr)	not specified [RCV004672445]	uncertain significance	5	129027321	129027321	Human		name
597701167	CV3602742	single nucleotide variant	NM_001017372.3(SLC27A6):c.1202A>G (p.Gln401Arg)	not specified [RCV004859952]	uncertain significance	5	129023657	129023657	Human		name
597755275	CV3602743	single nucleotide variant	NM_001017372.3(SLC27A6):c.1537G>C (p.Gly513Arg)	not specified [RCV004868107]	uncertain significance	5	129028427	129028427	Human		name
597755279	CV3602744	single nucleotide variant	NM_001017372.3(SLC27A6):c.1600A>G (p.Thr534Ala)	not specified [RCV004868108]	uncertain significance	5	129029624	129029624	Human		name
597755285	CV3602746	single nucleotide variant	NM_001017372.3(SLC27A6):c.1429T>G (p.Trp477Gly)	not specified [RCV004868110]	uncertain significance	5	129027306	129027306	Human		name
597701175	CV3602750	single nucleotide variant	NM_001017372.3(SLC27A6):c.1130T>C (p.Ile377Thr)	not specified [RCV004859953]	uncertain significance	5	129016045	129016045	Human		name
597755305	CV3602752	single nucleotide variant	NM_001017372.3(SLC27A6):c.1435C>A (p.Arg479Ser)	not specified [RCV004868115]	uncertain significance	5	129027312	129027312	Human		name
597755307	CV3602753	single nucleotide variant	NM_001017372.3(SLC27A6):c.1022G>T (p.Arg341Leu)	not specified [RCV004868116]	uncertain significance	5	129015937	129015937	Human		name
597755311	CV3602754	single nucleotide variant	NM_001017372.3(SLC27A6):c.1172C>A (p.Ser391Tyr)	not specified [RCV004868117]	uncertain significance	5	129023627	129023627	Human		name
598169697	CV3918418	single nucleotide variant	NM_001017372.3(SLC27A6):c.1280G>T (p.Arg427Leu)	not specified [RCV005284339]	uncertain significance	5	129027157	129027157	Human		name
598169703	CV3918420	single nucleotide variant	NM_001017372.3(SLC27A6):c.1354G>A (p.Val452Ile)	not specified [RCV005284341]	uncertain significance	5	129027231	129027231	Human		name
598236983	CV3918424	single nucleotide variant	NM_001017372.3(SLC27A6):c.1282G>C (p.Val428Leu)	not specified [RCV005275562]	uncertain significance	5	129027159	129027159	Human		name
8631369	CV86530	single nucleotide variant	NM_001017372.1(SLC27A6):c.1477A>G (p.Thr493Ala)	Malignant melanoma [RCV000066621]	not provided	5	129028367	129028367	Human		name
155741839	CV1770610	insertion	NM_001017372.3(SLC27A6):c.452_453insAGGAATCACCACACTGTCTTCCACAATGGTTGAACTAGTTTACAC (p.Cys151Ter)	Hepatocellular carcinoma [RCV002302835]	pathogenic	5	128966589	128966590	Human	1	name

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