Btn1a1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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47 records found for search term Btn1a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405710991	CV3298638	single nucleotide variant	NM_001732.3(BTN1A1):c.13C>T (p.Pro5Ser)	not specified [RCV004426808]	uncertain significance	6	26501299	26501299	Human		name
407500632	CV3417771	single nucleotide variant	NM_001732.3(BTN1A1):c.16A>G (p.Ser6Gly)	not specified [RCV004607176]	uncertain significance	6	26501302	26501302	Human		name
156302193	CV2241730	single nucleotide variant	NM_001732.3(BTN1A1):c.50T>C (p.Ile17Thr)	not specified [RCV004106673]	uncertain significance	6	26501336	26501336	Human		name
598186699	CV3949819	single nucleotide variant	NM_001732.3(BTN1A1):c.32G>C (p.Arg11Thr)	not specified [RCV005311900]	uncertain significance	6	26501318	26501318	Human		name
15141730	CV710372	single nucleotide variant	NM_001732.3(BTN1A1):c.882A>G (p.Lys294=)	not provided [RCV000966353]	benign	6	26508062	26508062	Human		name
8626144	CV81288	single nucleotide variant	NM_001732.2(BTN1A1):c.543G>A (p.Lys181=)	Malignant melanoma [RCV000061366]	not provided	6	26505040	26505040	Human		name
156331920	CV2218233	single nucleotide variant	NM_001732.3(BTN1A1):c.182T>C (p.Leu61Ser)	not specified [RCV004088433]	uncertain significance	6	26501692	26501692	Human		name
156118056	CV2349523	single nucleotide variant	NM_001732.3(BTN1A1):c.205A>G (p.Lys69Glu)	not specified [RCV004201487]	uncertain significance	6	26501715	26501715	Human		name
401882896	CV2775153	single nucleotide variant	NM_001732.3(BTN1A1):c.239G>C (p.Gly80Ala)	not specified [RCV004346508]	uncertain significance	6	26501749	26501749	Human		name
401864743	CV2791342	single nucleotide variant	NM_001732.3(BTN1A1):c.169A>T (p.Ser57Cys)	not specified [RCV004358751]	uncertain significance	6	26501679	26501679	Human		name
597784934	CV3647140	single nucleotide variant	NM_001732.3(BTN1A1):c.161C>G (p.Pro54Arg)	not specified [RCV004900609]	uncertain significance	6	26501671	26501671	Human		name
598186706	CV3949820	single nucleotide variant	NM_001732.3(BTN1A1):c.227T>G (p.Val76Gly)	not specified [RCV005311901]	uncertain significance	6	26501737	26501737	Human		name
598186738	CV3949827	single nucleotide variant	NM_001732.3(BTN1A1):c.173C>G (p.Ala58Gly)	not specified [RCV005311906]	uncertain significance	6	26501683	26501683	Human		name
8631941	CV87147	single nucleotide variant	NM_001732.2(BTN1A1):c.1239C>A (p.Leu413=)	Malignant melanoma [RCV000067238]	not provided	6	26508832	26508832	Human		name
156294145	CV2233611	single nucleotide variant	NM_001732.3(BTN1A1):c.764T>C (p.Met255Thr)	not specified [RCV004100078]	uncertain significance	6	26506737	26506737	Human		name
156043448	CV2237451	single nucleotide variant	NM_001732.3(BTN1A1):c.785T>C (p.Ile262Thr)	not specified [RCV004106412]	uncertain significance	6	26506758	26506758	Human		name
156127812	CV2244727	single nucleotide variant	NM_001732.3(BTN1A1):c.420G>T (p.Lys140Asn)	not specified [RCV004102723]	uncertain significance	6	26501930	26501930	Human		name
155904296	CV2275874	single nucleotide variant	NM_001732.3(BTN1A1):c.497C>T (p.Ser166Leu)	not specified [RCV004139534]	uncertain significance	6	26504994	26504994	Human		name
156331970	CV2339715	single nucleotide variant	NM_001732.3(BTN1A1):c.545G>C (p.Gly182Ala)	not specified [RCV004196417]	uncertain significance	6	26505042	26505042	Human		name
155910971	CV2366774	single nucleotide variant	NM_001732.3(BTN1A1):c.314G>C (p.Gly105Ala)	not specified [RCV004210767]	uncertain significance	6	26501824	26501824	Human		name
329381462	CV2437499	single nucleotide variant	NM_001732.3(BTN1A1):c.512C>G (p.Pro171Arg)	not specified [RCV004258786]	uncertain significance	6	26505009	26505009	Human		name
405711011	CV3298641	single nucleotide variant	NM_001732.3(BTN1A1):c.626G>T (p.Arg209Ile)	not specified [RCV004426811]	uncertain significance	6	26505123	26505123	Human		name
405711017	CV3298642	single nucleotide variant	NM_001732.3(BTN1A1):c.815A>G (p.Tyr272Cys)	not specified [RCV004426812]	uncertain significance	6	26506788	26506788	Human		name
407489707	CV3417768	single nucleotide variant	NM_001732.3(BTN1A1):c.638C>T (p.Ala213Val)	not specified [RCV004604116]	likely benign	6	26505135	26505135	Human		name
407489701	CV3417769	single nucleotide variant	NM_001732.3(BTN1A1):c.836G>A (p.Arg279Lys)	not specified [RCV004604117]	uncertain significance	6	26506809	26506809	Human		name
407489534	CV3417770	single nucleotide variant	NM_001732.3(BTN1A1):c.736T>A (p.Trp246Arg)	not specified [RCV004604118]	uncertain significance	6	26506709	26506709	Human		name
597784941	CV3647142	single nucleotide variant	NM_001732.3(BTN1A1):c.704T>C (p.Ile235Thr)	not specified [RCV004900611]	uncertain significance	6	26505201	26505201	Human		name
597784947	CV3647146	single nucleotide variant	NM_001732.3(BTN1A1):c.734C>T (p.Pro245Leu)	not specified [RCV004900613]	uncertain significance	6	26506707	26506707	Human		name
597784951	CV3647147	single nucleotide variant	NM_001732.3(BTN1A1):c.544G>A (p.Gly182Arg)	not specified [RCV004900614]	uncertain significance	6	26505041	26505041	Human		name
598211288	CV3949822	single nucleotide variant	NM_001732.3(BTN1A1):c.991C>T (p.Arg331Cys)	not specified [RCV005315988]	uncertain significance	6	26508584	26508584	Human		name
598186746	CV3949828	single nucleotide variant	NM_001732.3(BTN1A1):c.505T>A (p.Trp169Arg)	not specified [RCV005311907]	uncertain significance	6	26505002	26505002	Human		name
15104100	CV699490	single nucleotide variant	NM_001732.3(BTN1A1):c.876A>C (p.Glu292Asp)	not provided [RCV000959614]	benign	6	26507966	26507966	Human		name
156263056	CV2377113	single nucleotide variant	NM_001732.3(BTN1A1):c.1346A>G (p.Asn449Ser)	not specified [RCV004229784]	uncertain significance	6	26508939	26508939	Human		name
405710971	CV3298635	single nucleotide variant	NM_001732.3(BTN1A1):c.1048C>T (p.Arg350Cys)	not specified [RCV004426805]	uncertain significance	6	26508641	26508641	Human		name
405710979	CV3298636	single nucleotide variant	NM_001732.3(BTN1A1):c.1102A>G (p.Thr368Ala)	not specified [RCV004426806]	uncertain significance	6	26508695	26508695	Human		name
405710984	CV3298637	single nucleotide variant	NM_001732.3(BTN1A1):c.1252C>A (p.Pro418Thr)	not specified [RCV004426807]	uncertain significance	6	26508845	26508845	Human		name
405710998	CV3298639	single nucleotide variant	NM_001732.3(BTN1A1):c.1496C>T (p.Pro499Leu)	not specified [RCV004426809]	uncertain significance	6	26509089	26509089	Human		name
405711006	CV3298640	single nucleotide variant	NM_001732.3(BTN1A1):c.1564A>T (p.Ser522Cys)	not specified [RCV004426810]	uncertain significance	6	26509157	26509157	Human		name
597784930	CV3647139	single nucleotide variant	NM_001732.3(BTN1A1):c.1201A>G (p.Asn401Asp)	not specified [RCV004900608]	uncertain significance	6	26508794	26508794	Human		name
597784937	CV3647141	single nucleotide variant	NM_001732.3(BTN1A1):c.1186G>A (p.Val396Ile)	not specified [RCV004900610]	uncertain significance	6	26508779	26508779	Human		name
597749783	CV3647143	single nucleotide variant	NM_001732.3(BTN1A1):c.1166C>T (p.Pro389Leu)	not specified [RCV004892427]	uncertain significance	6	26508759	26508759	Human		name
597784944	CV3647145	single nucleotide variant	NM_001732.3(BTN1A1):c.1493C>T (p.Ser498Phe)	not specified [RCV004900612]	uncertain significance	6	26509086	26509086	Human		name
598186712	CV3949821	single nucleotide variant	NM_001732.3(BTN1A1):c.1223C>A (p.Pro408His)	not specified [RCV005311902]	uncertain significance	6	26508816	26508816	Human		name
598186719	CV3949823	single nucleotide variant	NM_001732.3(BTN1A1):c.1262G>A (p.Arg421Gln)	not specified [RCV005311903]	likely benign	6	26508855	26508855	Human		name
598186725	CV3949824	single nucleotide variant	NM_001732.3(BTN1A1):c.1024G>C (p.Asp342His)	not specified [RCV005311904]	uncertain significance	6	26508617	26508617	Human		name
598211296	CV3949825	single nucleotide variant	NM_001732.3(BTN1A1):c.1139T>C (p.Met380Thr)	not specified [RCV005315989]	uncertain significance	6	26508732	26508732	Human		name
15171671	CV710373	single nucleotide variant	NM_001732.3(BTN1A1):c.1571G>A (p.Gly524Glu)	not provided [RCV000972245]	benign	6	26509164	26509164	Human		name

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