Ubtfl1 Variant Search Result - Rat Genome Database

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25 records found for search term Ubtfl1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156190802	CV2226937	single nucleotide variant	NM_001143975.1(UBTFL1):c.211G>A (p.Gly71Ser)	not specified [RCV004103908]	uncertain significance	11	90086160	90086160	Human		name
156311152	CV2260134	single nucleotide variant	NM_001143975.1(UBTFL1):c.290C>G (p.Pro97Arg)	not specified [RCV004119130]	uncertain significance	11	90086239	90086239	Human		name
401744974	CV2681162	single nucleotide variant	NM_001143975.1(UBTFL1):c.275A>G (p.Lys92Arg)	not specified [RCV004296213]	uncertain significance	11	90086224	90086224	Human		name
401723695	CV2724998	single nucleotide variant	NM_001143975.1(UBTFL1):c.103A>G (p.Ser35Gly)	not specified [RCV004319757]	uncertain significance	11	90086052	90086052	Human		name
407523097	CV3491204	single nucleotide variant	NM_001143975.1(UBTFL1):c.145A>C (p.Lys49Gln)	not specified [RCV004677926]	uncertain significance	11	90086094	90086094	Human		name
597684746	CV3622728	single nucleotide variant	NM_001143975.1(UBTFL1):c.278A>G (p.Tyr93Cys)	not specified [RCV004883975]	uncertain significance	11	90086227	90086227	Human		name
597684756	CV3622729	single nucleotide variant	NM_001143975.1(UBTFL1):c.187A>T (p.Ile63Phe)	not specified [RCV004883976]	uncertain significance	11	90086136	90086136	Human		name
156330705	CV2224305	single nucleotide variant	NM_001143975.1(UBTFL1):c.755T>C (p.Val252Ala)	not specified [RCV004096125]	uncertain significance	11	90086704	90086704	Human		name
156098171	CV2306439	single nucleotide variant	NM_001143975.1(UBTFL1):c.523G>A (p.Val175Ile)	not specified [RCV004157065]	uncertain significance	11	90086472	90086472	Human		name
156084723	CV2366094	single nucleotide variant	NM_001143975.1(UBTFL1):c.994G>C (p.Gly332Arg)	not specified [RCV004210129]	uncertain significance	11	90086943	90086943	Human		name
156042576	CV2381468	single nucleotide variant	NM_001143975.1(UBTFL1):c.546T>G (p.Ser182Arg)	not specified [RCV004229949]	uncertain significance	11	90086495	90086495	Human		name
401779891	CV2676723	single nucleotide variant	NM_001143975.1(UBTFL1):c.600A>T (p.Glu200Asp)	not specified [RCV004290898]	uncertain significance	11	90086549	90086549	Human		name
401878410	CV2774299	single nucleotide variant	NM_001143975.1(UBTFL1):c.416G>A (p.Arg139Lys)	not specified [RCV004347661]	likely benign	11	90086365	90086365	Human		name
401905617	CV2813651	single nucleotide variant	NM_001143975.1(UBTFL1):c.920G>A (p.Gly307Asp)	not provided [RCV003395995]	likely benign	11	90086869	90086869	Human		name
405800346	CV3337834	single nucleotide variant	NM_001143975.1(UBTFL1):c.337G>A (p.Glu113Lys)	not specified [RCV004477221]	uncertain significance	11	90086286	90086286	Human		name
405800348	CV3337835	single nucleotide variant	NM_001143975.1(UBTFL1):c.460C>T (p.Arg154Trp)	not specified [RCV004477222]	uncertain significance	11	90086409	90086409	Human		name
405800350	CV3337836	single nucleotide variant	NM_001143975.1(UBTFL1):c.461G>A (p.Arg154Gln)	not specified [RCV004477223]	likely benign	11	90086410	90086410	Human		name
405800352	CV3337837	single nucleotide variant	NM_001143975.1(UBTFL1):c.518A>G (p.Asp173Gly)	not specified [RCV004477224]	uncertain significance	11	90086467	90086467	Human		name
405800354	CV3337838	single nucleotide variant	NM_001143975.1(UBTFL1):c.529A>G (p.Lys177Glu)	not specified [RCV004477225]	uncertain significance	11	90086478	90086478	Human		name
407462378	CV3491205	single nucleotide variant	NM_001143975.1(UBTFL1):c.781A>C (p.Ile261Leu)	not specified [RCV004687938]	uncertain significance	11	90086730	90086730	Human		name
597684725	CV3622726	single nucleotide variant	NM_001143975.1(UBTFL1):c.716G>C (p.Ser239Thr)	not specified [RCV004883973]	uncertain significance	11	90086665	90086665	Human		name
597684735	CV3622727	single nucleotide variant	NM_001143975.1(UBTFL1):c.528G>C (p.Gln176His)	not specified [RCV004883974]	uncertain significance	11	90086477	90086477	Human		name
597684764	CV3622730	single nucleotide variant	NM_001143975.1(UBTFL1):c.375G>A (p.Met125Ile)	not specified [RCV004883977]	uncertain significance	11	90086324	90086324	Human		name
597684773	CV3622731	single nucleotide variant	NM_001143975.1(UBTFL1):c.626A>G (p.Asp209Gly)	not specified [RCV004883978]	uncertain significance	11	90086575	90086575	Human		name
598190007	CV3929093	single nucleotide variant	NM_001143975.1(UBTFL1):c.761T>C (p.Ile254Thr)	not specified [RCV005288150]	uncertain significance	11	90086710	90086710	Human		name

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