Usp26 Variant Search Result - Rat Genome Database

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81 records found for search term Usp26

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401929471	CV2824034	single nucleotide variant	NM_031907.3(USP26):c.39G>A (p.Gly13=)	not provided [RCV003439866]	likely benign	X	133028182	133028182	Human		name
150411945	CV1196307	single nucleotide variant	NM_031907.3(USP26):c.20G>A (p.Arg7His)	not provided [RCV001573897]\|not specified [RCV004686681]	likely benign	X	133028201	133028201	Human		name
15143691	CV786701	single nucleotide variant	NM_031907.3(USP26):c.258A>G (p.Leu86=)	not provided [RCV000983369]	likely benign	X	133027963	133027963	Human		name
150484753	CV1263244	single nucleotide variant	NM_031907.3(USP26):c.576G>A (p.Glu192=)	USP26-related disorder [RCV003984057]\|not provided [RCV001686644]	benign	X	133027645	133027645	Human	1	name , trait , alternate_id
156238055	CV2193606	single nucleotide variant	NM_031907.3(USP26):c.74C>A (p.Ala25Glu)	not specified [RCV004074212]	uncertain significance	X	133028147	133028147	Human		name
156149256	CV2292929	single nucleotide variant	NM_031907.3(USP26):c.80T>C (p.Ile27Thr)	not specified [RCV004148423]	uncertain significance	X	133028141	133028141	Human		name
401929462	CV2824031	single nucleotide variant	NM_031907.3(USP26):c.924A>G (p.Ala308=)	not provided [RCV003439863]	likely benign	X	133027297	133027297	Human		name
405291501	CV3205732	single nucleotide variant	NM_031907.3(USP26):c.885C>T (p.His295=)	USP26-related disorder [RCV003963870]	likely benign	X	133027336	133027336	Human		name , trait , alternate_id
15201992	CV729418	single nucleotide variant	NM_031907.3(USP26):c.822C>T (p.Asp274=)	USP26-related disorder [RCV003940688]\|not provided [RCV000891352]	benign	X	133027399	133027399	Human	1	name , trait , alternate_id
155981201	CV2272821	single nucleotide variant	NM_031907.3(USP26):c.289T>C (p.Phe97Leu)	not specified [RCV004135728]	uncertain significance	X	133027932	133027932	Human		name
155969305	CV2391562	single nucleotide variant	NM_031907.3(USP26):c.152G>T (p.Arg51Leu)	not specified [RCV004239942]	uncertain significance	X	133028069	133028069	Human		name
405294074	CV3203408	single nucleotide variant	NM_031907.3(USP26):c.1500G>A (p.Glu500=)	USP26-related disorder [RCV003933952]	likely benign	X	133026721	133026721	Human		name , trait , alternate_id
405260386	CV3209174	single nucleotide variant	NM_031907.3(USP26):c.1992C>G (p.Thr664=)	USP26-related disorder [RCV003943875]	likely benign	X	133026229	133026229	Human		name , trait , alternate_id
405271357	CV3209332	single nucleotide variant	NM_031907.3(USP26):c.1983G>T (p.Leu661=)	USP26-related disorder [RCV003949673]	likely benign	X	133026238	133026238	Human		name , trait , alternate_id
596944245	CV3398631	single nucleotide variant	NM_031907.3(USP26):c.125T>C (p.Phe42Ser)	Abnormal sperm morphology [RCV004801448]	uncertain significance	X	133028096	133028096	Human	4	name
407455296	CV3487500	single nucleotide variant	NM_031907.3(USP26):c.221C>T (p.Thr74Ile)	not specified [RCV004685501]	uncertain significance	X	133028000	133028000	Human		name
15175129	CV706106	single nucleotide variant	NM_031907.3(USP26):c.2088A>G (p.Pro696=)	USP26-related disorder [RCV003925932]\|not provided [RCV000950504]	benign\|likely benign	X	133026133	133026133	Human	1	name , trait , alternate_id
15200025	CV758297	single nucleotide variant	NM_031907.3(USP26):c.1887T>C (p.Leu629=)	not provided [RCV000912723]	likely benign	X	133026334	133026334	Human		name
15117062	CV773760	single nucleotide variant	NM_031907.3(USP26):c.151C>T (p.Arg51Trp)	not provided [RCV000939771]	likely benign	X	133028070	133028070	Human		name
155962334	CV1936599	deletion	NM_031907.3(USP26):c.1578del (p.Asn527fs)	not provided [RCV002512418]	uncertain significance	X	133026643	133026643	Human		name
155965670	CV2330596	single nucleotide variant	NM_031907.3(USP26):c.463C>T (p.Leu155Phe)	not specified [RCV004183193]	uncertain significance	X	133027758	133027758	Human		name
329374746	CV2470700	single nucleotide variant	NM_031907.3(USP26):c.731C>G (p.Thr244Ser)	not specified [RCV004275948]	uncertain significance	X	133027490	133027490	Human		name
401769681	CV2689887	single nucleotide variant	NM_031907.3(USP26):c.316G>T (p.Val106Phe)	not specified [RCV004297782]	uncertain significance	X	133027905	133027905	Human		name
401762110	CV2699523	single nucleotide variant	NM_031907.3(USP26):c.376G>C (p.Glu126Gln)	not specified [RCV004299731]	uncertain significance	X	133027845	133027845	Human		name
401929465	CV2824032	single nucleotide variant	NM_031907.3(USP26):c.508G>A (p.Gly170Arg)	not provided [RCV003439864]	likely benign	X	133027713	133027713	Human		name
401929467	CV2824033	single nucleotide variant	NM_031907.3(USP26):c.338G>T (p.Gly113Val)	not provided [RCV003439865]\|not specified [RCV004364669]	likely benign\|uncertain significance	X	133027883	133027883	Human		name
405292287	CV3199858	single nucleotide variant	NM_031907.3(USP26):c.494T>C (p.Leu165Ser)	USP26-related disorder [RCV003964433]	benign	X	133027727	133027727	Human		name , trait , alternate_id
405814957	CV3341801	single nucleotide variant	NM_031907.3(USP26):c.853T>A (p.Phe285Ile)	not specified [RCV004484687]	uncertain significance	X	133027368	133027368	Human		name
407455300	CV3487502	single nucleotide variant	NM_031907.3(USP26):c.682G>C (p.Glu228Gln)	not specified [RCV004685503]	uncertain significance	X	133027539	133027539	Human		name
597798560	CV3626261	single nucleotide variant	NM_031907.3(USP26):c.818G>A (p.Ser273Asn)	not specified [RCV004879253]	uncertain significance	X	133027403	133027403	Human		name
597798566	CV3626264	single nucleotide variant	NM_031907.3(USP26):c.596A>G (p.Asn199Ser)	not specified [RCV004879256]	uncertain significance	X	133027625	133027625	Human		name
597798568	CV3626265	single nucleotide variant	NM_031907.3(USP26):c.343G>A (p.Gly115Ser)	not specified [RCV004879257]	uncertain significance	X	133027878	133027878	Human		name
156397488	CV2200603	single nucleotide variant	NM_031907.3(USP26):c.1535G>A (p.Arg512Lys)	not specified [RCV004078943]	uncertain significance	X	133026686	133026686	Human		name
156090286	CV2206574	single nucleotide variant	NM_031907.3(USP26):c.1529T>G (p.Phe510Cys)	not specified [RCV004080919]	uncertain significance	X	133026692	133026692	Human		name
156379577	CV2211440	single nucleotide variant	NM_031907.3(USP26):c.2715G>T (p.Glu905Asp)	not specified [RCV004090669]	uncertain significance	X	133025506	133025506	Human		name
156193090	CV2223237	single nucleotide variant	NM_031907.3(USP26):c.2624G>A (p.Arg875His)	not specified [RCV004105859]	uncertain significance	X	133025597	133025597	Human		name
156185009	CV2239311	single nucleotide variant	NM_031907.3(USP26):c.1876C>A (p.Gln626Lys)	not specified [RCV004114056]	uncertain significance	X	133026345	133026345	Human		name
156059170	CV2239312	single nucleotide variant	NM_031907.3(USP26):c.1954G>C (p.Glu652Gln)	not specified [RCV004114057]	uncertain significance	X	133026267	133026267	Human		name
156073296	CV2240679	single nucleotide variant	NM_031907.3(USP26):c.1354G>A (p.Gly452Ser)	not specified [RCV004119310]	uncertain significance	X	133026867	133026867	Human		name
155912583	CV2245585	single nucleotide variant	NM_031907.3(USP26):c.2457G>T (p.Lys819Asn)	not specified [RCV004109661]	uncertain significance	X	133025764	133025764	Human		name
155914797	CV2264681	single nucleotide variant	NM_031907.3(USP26):c.2198A>G (p.Gln733Arg)	not specified [RCV004132678]	uncertain significance	X	133026023	133026023	Human		name
155978039	CV2338902	single nucleotide variant	NM_031907.3(USP26):c.2230G>A (p.Gly744Ser)	not specified [RCV004184495]	uncertain significance	X	133025991	133025991	Human		name
156221519	CV2392501	single nucleotide variant	NM_031907.3(USP26):c.1994C>T (p.Ser665Leu)	not specified [RCV004244070]	uncertain significance	X	133026227	133026227	Human		name
329351195	CV2418191	single nucleotide variant	NM_031907.3(USP26):c.2473C>G (p.Arg825Gly)	Spermatogenic failure, X-linked, 6 [RCV003153258]	pathogenic	X	133025748	133025748	Human	1	name
329351196	CV2418192	single nucleotide variant	NM_031907.3(USP26):c.2396A>G (p.Asn799Ser)	Spermatogenic failure, X-linked, 6 [RCV003153259]	pathogenic	X	133025825	133025825	Human	1	name
329392565	CV2438972	single nucleotide variant	NM_031907.3(USP26):c.1813G>A (p.Asp605Asn)	not specified [RCV004264482]	uncertain significance	X	133026408	133026408	Human		name
329349974	CV2477129	duplication	NM_031907.3(USP26):c.1044dup (p.Lys349Ter)	not provided [RCV003221454]	uncertain significance	X	133027176	133027177	Human		name
401940631	CV2671984	single nucleotide variant	NM_031907.3(USP26):c.1205A>C (p.Asn402Thr)	Male infertility [RCV004585024]\|Spermatogenic failure, X-linked, 6 [RCV003459816]	pathogenic	X	133027016	133027016	Human	3	name
401750073	CV2704963	single nucleotide variant	NM_031907.3(USP26):c.1348G>A (p.Ala450Thr)	not specified [RCV004307529]	uncertain significance	X	133026873	133026873	Human		name
401887147	CV2775661	single nucleotide variant	NM_031907.3(USP26):c.1231T>C (p.Phe411Leu)	not specified [RCV004350802]	uncertain significance	X	133026990	133026990	Human		name
401869772	CV2782475	single nucleotide variant	NM_031907.3(USP26):c.2140A>G (p.Ile714Val)	not specified [RCV004359526]	uncertain significance	X	133026081	133026081	Human		name
401929454	CV2824028	single nucleotide variant	NM_031907.3(USP26):c.2738A>G (p.Glu913Gly)	not provided [RCV003439860]	likely benign	X	133025483	133025483	Human		name
401929457	CV2824029	single nucleotide variant	NM_031907.3(USP26):c.2327C>T (p.Thr776Ile)	not provided [RCV003439861]	likely benign	X	133025894	133025894	Human		name
401929459	CV2824030	single nucleotide variant	NM_031907.3(USP26):c.2062G>A (p.Asp688Asn)	not provided [RCV003439862]	likely benign	X	133026159	133026159	Human		name
405266112	CV3215840	single nucleotide variant	NM_031907.3(USP26):c.2009A>G (p.His670Arg)	USP26-related disorder [RCV003946987]	likely benign	X	133026212	133026212	Human		name , trait , alternate_id
405278555	CV3221958	single nucleotide variant	NM_031907.3(USP26):c.1423C>T (p.His475Tyr)	USP26-related disorder [RCV003976500]	benign	X	133026798	133026798	Human		name , trait , alternate_id
405814946	CV3341795	single nucleotide variant	NM_031907.3(USP26):c.1097A>C (p.Lys366Thr)	not specified [RCV004484681]	uncertain significance	X	133027124	133027124	Human		name
405814948	CV3341796	single nucleotide variant	NM_031907.3(USP26):c.1279A>G (p.Thr427Ala)	not specified [RCV004484682]	uncertain significance	X	133026942	133026942	Human		name
405814950	CV3341797	single nucleotide variant	NM_031907.3(USP26):c.1581T>G (p.Asn527Lys)	not specified [RCV004484683]	uncertain significance	X	133026640	133026640	Human		name
405814953	CV3341799	single nucleotide variant	NM_031907.3(USP26):c.1934A>G (p.Asp645Gly)	not specified [RCV004484685]	uncertain significance	X	133026287	133026287	Human		name
405814955	CV3341800	single nucleotide variant	NM_031907.3(USP26):c.2614G>A (p.Glu872Lys)	not specified [RCV004484686]	likely benign	X	133025607	133025607	Human		name
407455298	CV3487501	single nucleotide variant	NM_031907.3(USP26):c.1837G>C (p.Gly613Arg)	not specified [RCV004685502]	uncertain significance	X	133026384	133026384	Human		name
407455302	CV3487503	single nucleotide variant	NM_031907.3(USP26):c.1256A>T (p.Gln419Leu)	not specified [RCV004685504]	uncertain significance	X	133026965	133026965	Human		name
597723209	CV3626259	single nucleotide variant	NM_031907.3(USP26):c.2582G>A (p.Arg861Gln)	not specified [RCV004888063]	likely benign	X	133025639	133025639	Human		name
597723224	CV3626260	single nucleotide variant	NM_031907.3(USP26):c.1297C>T (p.Pro433Ser)	not specified [RCV004888064]	uncertain significance	X	133026924	133026924	Human		name
597798562	CV3626262	single nucleotide variant	NM_031907.3(USP26):c.1031G>A (p.Arg344Gln)	not specified [RCV004879254]	likely benign	X	133027190	133027190	Human		name
597798570	CV3626266	single nucleotide variant	NM_031907.3(USP26):c.2093G>A (p.Arg698Gln)	not specified [RCV004879258]	likely benign	X	133026128	133026128	Human		name
597798572	CV3626267	single nucleotide variant	NM_031907.3(USP26):c.2646T>G (p.Phe882Leu)	not specified [RCV004879259]	uncertain significance	X	133025575	133025575	Human		name
597798574	CV3626268	single nucleotide variant	NM_031907.3(USP26):c.1837G>A (p.Gly613Ser)	not specified [RCV004879260]	uncertain significance	X	133026384	133026384	Human		name
597798577	CV3626269	single nucleotide variant	NM_031907.3(USP26):c.2140A>T (p.Ile714Phe)	not specified [RCV004879261]	uncertain significance	X	133026081	133026081	Human		name
598275207	CV3936571	single nucleotide variant	NM_031907.3(USP26):c.1513G>T (p.Val505Phe)	not specified [RCV005304341]	uncertain significance	X	133026708	133026708	Human		name
598275208	CV3936572	single nucleotide variant	NM_031907.3(USP26):c.1589G>T (p.Cys530Phe)	not specified [RCV005304342]	uncertain significance	X	133026632	133026632	Human		name
598203872	CV3936573	single nucleotide variant	NM_031907.3(USP26):c.2075T>A (p.Val692Glu)	not specified [RCV005290603]	uncertain significance	X	133026146	133026146	Human		name
598275209	CV3936574	single nucleotide variant	NM_031907.3(USP26):c.2464C>G (p.His822Asp)	not specified [RCV005304343]	uncertain significance	X	133025757	133025757	Human		name
598203881	CV3936575	single nucleotide variant	NM_031907.3(USP26):c.2603C>A (p.Ala868Asp)	not specified [RCV005290604]	uncertain significance	X	133025618	133025618	Human		name
598203889	CV3936576	single nucleotide variant	NM_031907.3(USP26):c.1921G>C (p.Val641Leu)	not specified [RCV005290605]	uncertain significance	X	133026300	133026300	Human		name
598203897	CV3936577	single nucleotide variant	NM_031907.3(USP26):c.1568G>A (p.Arg523His)	not specified [RCV005290606]	uncertain significance	X	133026653	133026653	Human		name
598203903	CV3936578	single nucleotide variant	NM_031907.3(USP26):c.1472A>G (p.Glu491Gly)	not specified [RCV005290607]	uncertain significance	X	133026749	133026749	Human		name
15198252	CV729416	single nucleotide variant	NM_031907.3(USP26):c.1976C>T (p.Thr659Met)	not provided [RCV000890300]	likely benign	X	133026245	133026245	Human		name
15170912	CV729417	single nucleotide variant	NM_031907.3(USP26):c.1737G>A (p.Met579Ile)	USP26-related disorder [RCV003920591]\|not provided [RCV000883557]	benign\|likely benign	X	133026484	133026484	Human	1	name , trait , alternate_id
150457852	CV1260198	microsatellite	NM_031907.3(USP26):c.364ACA[3] (p.Thr123dup)	USP26-related disorder [RCV003968469]\|not provided [RCV001681678]	benign	X	133027851	133027852	Human		name , trait , alternate_id

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