Cytl1 Variant Search Result - Rat Genome Database

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21 records found for search term Cytl1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407452750	CV3420305	single nucleotide variant	NM_018659.3(CYTL1):c.53C>G (p.Pro18Arg)	not specified [RCV004608654]	uncertain significance	4	5019393	5019393	Human		name
597674290	CV3655011	single nucleotide variant	NM_018659.3(CYTL1):c.37C>T (p.Leu13Phe)	not specified [RCV004913506]	uncertain significance	4	5019409	5019409	Human		name
598250571	CV3952685	single nucleotide variant	NM_018659.3(CYTL1):c.62G>T (p.Arg21Leu)	not specified [RCV005322904]	uncertain significance	4	5019384	5019384	Human		name
598250587	CV3952687	single nucleotide variant	NM_018659.3(CYTL1):c.82T>C (p.Tyr28His)	not specified [RCV005322906]	uncertain significance	4	5019364	5019364	Human		name
598250595	CV3952688	single nucleotide variant	NM_018659.3(CYTL1):c.83A>G (p.Tyr28Cys)	not specified [RCV005322907]	uncertain significance	4	5019363	5019363	Human		name
8625806	CV80930	single nucleotide variant	NM_018659.2(CYTL1):c.339C>T (p.Phe113=)	Malignant melanoma [RCV000061007]	not provided	4	5015223	5015223	Human		name
156315349	CV2192889	single nucleotide variant	NM_018659.3(CYTL1):c.230T>C (p.Phe77Ser)	not specified [RCV004069454]	uncertain significance	4	5016933	5016933	Human		name
156297935	CV2310569	single nucleotide variant	NM_018659.3(CYTL1):c.145G>C (p.Glu49Gln)	not specified [RCV004163586]	uncertain significance	4	5019301	5019301	Human		name
156167567	CV2345312	single nucleotide variant	NM_018659.3(CYTL1):c.245C>T (p.Pro82Leu)	not specified [RCV004198093]	uncertain significance	4	5016918	5016918	Human		name
405678714	CV3236523	single nucleotide variant	NM_018659.3(CYTL1):c.265G>A (p.Val89Ile)	not specified [RCV004370674]	uncertain significance	4	5016898	5016898	Human		name
407452748	CV3420304	single nucleotide variant	NM_018659.3(CYTL1):c.279G>C (p.Lys93Asn)	not specified [RCV004608653]	uncertain significance	4	5016884	5016884	Human		name
407452752	CV3420306	single nucleotide variant	NM_018659.3(CYTL1):c.142T>C (p.Ser48Pro)	not specified [RCV004608655]	uncertain significance	4	5019304	5019304	Human		name
598250562	CV3952684	single nucleotide variant	NM_018659.3(CYTL1):c.290G>A (p.Arg97Gln)	not specified [RCV005322903]	uncertain significance	4	5016873	5016873	Human		name
155919581	CV2254893	single nucleotide variant	NM_018659.3(CYTL1):c.400C>G (p.Arg134Gly)	not specified [RCV004117136]	uncertain significance	4	5015162	5015162	Human		name
156361989	CV2265456	single nucleotide variant	NM_018659.3(CYTL1):c.331T>G (p.Leu111Val)	not specified [RCV004124220]	uncertain significance	4	5015231	5015231	Human		name
155976702	CV2342808	single nucleotide variant	NM_018659.3(CYTL1):c.407G>A (p.Arg136His)	not specified [RCV004189849]	uncertain significance	4	5015155	5015155	Human		name
401761718	CV2726877	single nucleotide variant	NM_018659.3(CYTL1):c.395C>G (p.Pro132Arg)	not specified [RCV004323170]	uncertain significance	4	5015167	5015167	Human		name
401882773	CV2788585	single nucleotide variant	NM_018659.3(CYTL1):c.401G>A (p.Arg134His)	not specified [RCV004361082]	likely benign	4	5015161	5015161	Human		name
405678719	CV3236524	single nucleotide variant	NM_018659.3(CYTL1):c.386C>T (p.Thr129Met)	not specified [RCV004370675]	uncertain significance	4	5015176	5015176	Human		name
597674065	CV3655012	single nucleotide variant	NM_018659.3(CYTL1):c.352T>C (p.Cys118Arg)	not specified [RCV004913507]	uncertain significance	4	5015210	5015210	Human		name
598250579	CV3952686	single nucleotide variant	NM_018659.3(CYTL1):c.320G>T (p.Cys107Phe)	not specified [RCV005322905]	uncertain significance	4	5016843	5016843	Human		name

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