Oxsm Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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34 records found for search term Oxsm

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407478644	CV3469946	single nucleotide variant	NM_017897.3(OXSM):c.24C>A (p.Phe8Leu)	not specified [RCV004663948]	uncertain significance	3	25791044	25791044	Human		name
401745238	CV2693213	single nucleotide variant	NM_017897.3(OXSM):c.43C>T (p.Arg15Cys)	not specified [RCV004293141]	uncertain significance	3	25791063	25791063	Human		name
597656756	CV3578073	single nucleotide variant	NM_017897.3(OXSM):c.54T>G (p.Cys18Trp)	not specified [RCV004827533]	uncertain significance	3	25791074	25791074	Human		name
597656764	CV3578075	single nucleotide variant	NM_017897.3(OXSM):c.97G>A (p.Gly33Arg)	not specified [RCV004827534]	uncertain significance	3	25791117	25791117	Human		name
156252348	CV2286963	single nucleotide variant	NM_017897.3(OXSM):c.229G>A (p.Val77Ile)	not specified [RCV004144565]	uncertain significance	3	25791249	25791249	Human		name
156002209	CV2296491	single nucleotide variant	NM_017897.3(OXSM):c.256T>C (p.Cys86Arg)	not specified [RCV004148226]	uncertain significance	3	25791276	25791276	Human		name
156039152	CV2313708	single nucleotide variant	NM_017897.3(OXSM):c.122A>G (p.His41Arg)	not specified [RCV004157624]	likely benign	3	25791142	25791142	Human		name
155968736	CV2339344	single nucleotide variant	NM_017897.3(OXSM):c.176C>A (p.Thr59Asn)	not specified [RCV004191574]	uncertain significance	3	25791196	25791196	Human		name
401725510	CV2721805	single nucleotide variant	NM_017897.3(OXSM):c.275T>C (p.Val92Ala)	not specified [RCV004326323]	uncertain significance	3	25791295	25791295	Human		name
156095724	CV2210289	single nucleotide variant	NM_017897.3(OXSM):c.568G>T (p.Gly190Cys)	not specified [RCV004089453]	uncertain significance	3	25791588	25791588	Human		name
156127111	CV2223756	single nucleotide variant	NM_017897.3(OXSM):c.606T>A (p.Asn202Lys)	not specified [RCV004093839]	uncertain significance	3	25791626	25791626	Human		name
156382213	CV2227244	single nucleotide variant	NM_017897.3(OXSM):c.725C>T (p.Pro242Leu)	not specified [RCV004091827]	uncertain significance	3	25791745	25791745	Human		name
155990298	CV2285235	single nucleotide variant	NM_017897.3(OXSM):c.688G>A (p.Val230Met)	not specified [RCV004145434]	uncertain significance	3	25791708	25791708	Human		name
156004687	CV2296006	single nucleotide variant	NM_017897.3(OXSM):c.326A>C (p.Lys109Thr)	not specified [RCV004151891]	uncertain significance	3	25791346	25791346	Human		name
401888136	CV2791272	single nucleotide variant	NM_017897.3(OXSM):c.740G>C (p.Gly247Ala)	not specified [RCV004356902]	uncertain significance	3	25791760	25791760	Human		name
405738936	CV3371188	single nucleotide variant	NM_017897.3(OXSM):c.719T>C (p.Ile240Thr)	not specified [RCV004497437]	uncertain significance	3	25791739	25791739	Human		name
405738941	CV3371189	single nucleotide variant	NM_017897.3(OXSM):c.724C>G (p.Pro242Ala)	not specified [RCV004497438]	uncertain significance	3	25791744	25791744	Human		name
405738948	CV3371190	single nucleotide variant	NM_017897.3(OXSM):c.834A>C (p.Glu278Asp)	not specified [RCV004497439]	uncertain significance	3	25791854	25791854	Human		name
407517276	CV3469945	single nucleotide variant	NM_017897.3(OXSM):c.577A>G (p.Ser193Gly)	not specified [RCV004650611]	uncertain significance	3	25791597	25791597	Human		name
597692649	CV3578071	single nucleotide variant	NM_017897.3(OXSM):c.691A>G (p.Met231Val)	not specified [RCV004838833]	uncertain significance	3	25791711	25791711	Human		name
597692669	CV3578074	single nucleotide variant	NM_017897.3(OXSM):c.478G>A (p.Val160Ile)	not specified [RCV004838835]	likely benign	3	25791498	25791498	Human		name
598163150	CV3995805	single nucleotide variant	NM_017897.3(OXSM):c.325A>G (p.Lys109Glu)	not specified [RCV005390938]	uncertain significance	3	25791345	25791345	Human		name
598163164	CV3995807	single nucleotide variant	NM_017897.3(OXSM):c.622G>A (p.Ala208Thr)	not specified [RCV005390940]	uncertain significance	3	25791642	25791642	Human		name
598163171	CV3995808	single nucleotide variant	NM_017897.3(OXSM):c.508A>G (p.Lys170Glu)	not specified [RCV005390941]	uncertain significance	3	25791528	25791528	Human		name
598184365	CV3995809	single nucleotide variant	NM_017897.3(OXSM):c.842C>T (p.Ala281Val)	not specified [RCV005395440]	uncertain significance	3	25791862	25791862	Human		name
156387996	CV2221682	single nucleotide variant	NM_017897.3(OXSM):c.1090A>C (p.Lys364Gln)	not specified [RCV004098451]	uncertain significance	3	25794204	25794204	Human		name
156068509	CV2320438	single nucleotide variant	NM_017897.3(OXSM):c.1351A>C (p.Asn451His)	not specified [RCV004172081]	uncertain significance	3	25794465	25794465	Human		name
329382169	CV2424354	single nucleotide variant	NM_017897.3(OXSM):c.1315A>G (p.Ile439Val)	not specified [RCV004252258]	uncertain significance	3	25794429	25794429	Human		name
401869611	CV2772461	single nucleotide variant	NM_017897.3(OXSM):c.1276C>T (p.Pro426Ser)	not specified [RCV004355243]	uncertain significance	3	25794390	25794390	Human		name
405738913	CV3371185	single nucleotide variant	NM_017897.3(OXSM):c.1014G>C (p.Gln338His)	not specified [RCV004497434]	uncertain significance	3	25794128	25794128	Human		name
405738923	CV3371186	single nucleotide variant	NM_017897.3(OXSM):c.1037A>G (p.Asn346Ser)	not specified [RCV004497435]	uncertain significance	3	25794151	25794151	Human		name
405738929	CV3371187	single nucleotide variant	NM_017897.3(OXSM):c.1268A>G (p.Asn423Ser)	not specified [RCV004497436]	uncertain significance	3	25794382	25794382	Human		name
597692659	CV3578072	single nucleotide variant	NM_017897.3(OXSM):c.1139A>G (p.Lys380Arg)	not specified [RCV004838834]	uncertain significance	3	25794253	25794253	Human		name
598163157	CV3995806	single nucleotide variant	NM_017897.3(OXSM):c.1031A>G (p.Tyr344Cys)	not specified [RCV005390939]	uncertain significance	3	25794145	25794145	Human		name

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