Slc38a6 Variant Search Result - Rat Genome Database

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33 records found for search term Slc38a6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8627545	CV82689	single nucleotide variant	NM_001172702.1(SLC38A6):c.363+2T>G	Malignant melanoma [RCV000062769]	not provided	14	61015958	61015958	Human		name
401859253	CV2788997	single nucleotide variant	NM_153811.3(SLC38A6):c.67G>A (p.Glu23Lys)	not specified [RCV004363309]	uncertain significance	14	60981344	60981344	Human		name
401892384	CV2785366	single nucleotide variant	NM_153811.3(SLC38A6):c.181A>C (p.Ser61Arg)	not specified [RCV004357113]	uncertain significance	14	60982583	60982583	Human		name
405708752	CV3329069	single nucleotide variant	NM_153811.3(SLC38A6):c.118C>G (p.Gln40Glu)	not specified [RCV004461457]	uncertain significance	14	60982520	60982520	Human		name
405708762	CV3329070	single nucleotide variant	NM_153811.3(SLC38A6):c.283C>T (p.Leu95Phe)	not specified [RCV004461458]	uncertain significance	14	60984776	60984776	Human		name
407514696	CV3484558	single nucleotide variant	NM_153811.3(SLC38A6):c.127C>T (p.Pro43Ser)	not specified [RCV004674665]	uncertain significance	14	60982529	60982529	Human		name
407514707	CV3484561	single nucleotide variant	NM_153811.3(SLC38A6):c.185G>A (p.Gly62Asp)	not specified [RCV004674668]	uncertain significance	14	60982587	60982587	Human		name
597703146	CV3599915	single nucleotide variant	NM_153811.3(SLC38A6):c.172A>G (p.Ile58Val)	not specified [RCV004860167]	uncertain significance	14	60982574	60982574	Human		name
598243625	CV3914954	single nucleotide variant	NM_153811.3(SLC38A6):c.209T>C (p.Leu70Ser)	not specified [RCV005276735]	uncertain significance	14	60982611	60982611	Human		name
156397996	CV2194084	single nucleotide variant	NM_153811.3(SLC38A6):c.404C>G (p.Ala135Gly)	not specified [RCV004076843]	uncertain significance	14	61030445	61030445	Human		name
156332700	CV2214482	single nucleotide variant	NM_153811.3(SLC38A6):c.862G>A (p.Ala288Thr)	not specified [RCV004088537]	uncertain significance	14	61046104	61046104	Human		name
156221027	CV2222444	single nucleotide variant	NM_153811.3(SLC38A6):c.442C>T (p.Pro148Ser)	not specified [RCV004099298]	uncertain significance	14	61030483	61030483	Human		name
156079502	CV2226547	single nucleotide variant	NM_153811.3(SLC38A6):c.983T>C (p.Val328Ala)	not specified [RCV004101806]	uncertain significance	14	61050569	61050569	Human		name
156096781	CV2253141	single nucleotide variant	NM_153811.3(SLC38A6):c.793T>C (p.Ser265Pro)	not specified [RCV004120917]	uncertain significance	14	61045394	61045394	Human		name
156251511	CV2311298	single nucleotide variant	NM_153811.3(SLC38A6):c.313G>A (p.Val105Ile)	not specified [RCV004166375]	uncertain significance	14	61015906	61015906	Human		name
329379646	CV2443500	single nucleotide variant	NM_153811.3(SLC38A6):c.547G>A (p.Ala183Thr)	not specified [RCV004262335]	uncertain significance	14	61037123	61037123	Human		name
329388105	CV2468698	single nucleotide variant	NM_153811.3(SLC38A6):c.883A>G (p.Ile295Val)	not specified [RCV004280028]	uncertain significance	14	61046125	61046125	Human		name
401748883	CV2692834	single nucleotide variant	NM_153811.3(SLC38A6):c.524G>C (p.Cys175Ser)	not specified [RCV004306373]	uncertain significance	14	61037100	61037100	Human		name
401900038	CV2780237	single nucleotide variant	NM_153811.3(SLC38A6):c.617C>G (p.Ala206Gly)	not specified [RCV004355875]	uncertain significance	14	61037676	61037676	Human		name
405708766	CV3329071	single nucleotide variant	NM_153811.3(SLC38A6):c.428T>C (p.Ile143Thr)	not specified [RCV004461459]	uncertain significance	14	61030469	61030469	Human		name
405708772	CV3329072	single nucleotide variant	NM_153811.3(SLC38A6):c.673G>A (p.Val225Ile)	not specified [RCV004461460]	likely benign	14	61043195	61043195	Human		name
405708784	CV3329073	single nucleotide variant	NM_153811.3(SLC38A6):c.752A>G (p.Tyr251Cys)	not specified [RCV004461461]	uncertain significance	14	61045353	61045353	Human		name
405708789	CV3329074	single nucleotide variant	NM_153811.3(SLC38A6):c.988A>G (p.Met330Val)	not specified [RCV004461462]	uncertain significance	14	61050574	61050574	Human		name
407451632	CV3484557	single nucleotide variant	NM_153811.3(SLC38A6):c.817C>T (p.Leu273Phe)	not specified [RCV004683725]	uncertain significance	14	61045418	61045418	Human		name
407514700	CV3484559	single nucleotide variant	NM_153811.3(SLC38A6):c.384A>G (p.Ile128Met)	not specified [RCV004674666]	uncertain significance	14	61019561	61019561	Human		name
597765738	CV3599917	single nucleotide variant	NM_153811.3(SLC38A6):c.767T>C (p.Met256Thr)	not specified [RCV004870482]	uncertain significance	14	61045368	61045368	Human		name
598243616	CV3914953	single nucleotide variant	NM_153811.3(SLC38A6):c.494T>C (p.Leu165Pro)	not specified [RCV005276734]	uncertain significance	14	61037070	61037070	Human		name
598237215	CV3914956	single nucleotide variant	NM_153811.3(SLC38A6):c.707A>G (p.Asp236Gly)	not specified [RCV005275613]	uncertain significance	14	61043466	61043466	Human		name
598243643	CV3914957	single nucleotide variant	NM_153811.3(SLC38A6):c.408G>C (p.Met136Ile)	not specified [RCV005276737]	uncertain significance	14	61030449	61030449	Human		name
13827755	CV578512	single nucleotide variant	NM_153811.3(SLC38A6):c.323A>G (p.Tyr108Cys)	not provided [RCV000714758]	uncertain significance	14	61015916	61015916	Human		name
401750729	CV2700049	single nucleotide variant	NM_153811.3(SLC38A6):c.1232C>T (p.Pro411Leu)	not specified [RCV004310472]	uncertain significance	14	61052077	61052077	Human		name
407514703	CV3484560	single nucleotide variant	NM_153811.3(SLC38A6):c.1225A>G (p.Ile409Val)	not specified [RCV004674667]	likely benign	14	61052070	61052070	Human		name
597703156	CV3599916	single nucleotide variant	NM_153811.3(SLC38A6):c.1119C>G (p.Ile373Met)	not specified [RCV004860168]	uncertain significance	14	61051855	61051855	Human		name

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