Leng1 Variant Search Result - Rat Genome Database

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40 records found for search term Leng1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405817859	CV3280225	single nucleotide variant	NM_024316.3(LENG1):c.13C>T (p.Pro5Ser)	not specified [RCV004412732]	uncertain significance	19	54159683	54159683	Human		name
401764771	CV2705329	single nucleotide variant	NM_024316.3(LENG1):c.31G>C (p.Val11Leu)	not specified [RCV004312010]	uncertain significance	19	54159665	54159665	Human		name
407491905	CV3452693	single nucleotide variant	NM_024316.3(LENG1):c.56G>A (p.Arg19His)	not specified [RCV004642339]	uncertain significance	19	54159640	54159640	Human		name
407491909	CV3452694	single nucleotide variant	NM_024316.3(LENG1):c.92A>C (p.Glu31Ala)	not specified [RCV004642340]	uncertain significance	19	54159604	54159604	Human		name
597641100	CV3699046	single nucleotide variant	NM_024316.3(LENG1):c.76C>G (p.Gln26Glu)	not specified [RCV004941598]	uncertain significance	19	54159620	54159620	Human		name
155944880	CV2237884	single nucleotide variant	NM_024316.3(LENG1):c.289A>C (p.Lys97Gln)	not specified [RCV004109112]	uncertain significance	19	54158305	54158305	Human		name
156103521	CV2291618	single nucleotide variant	NM_024316.3(LENG1):c.181C>T (p.Pro61Ser)	not specified [RCV004155909]	uncertain significance	19	54158413	54158413	Human		name
401774283	CV2691680	single nucleotide variant	NM_024316.3(LENG1):c.278A>G (p.Asn93Ser)	not specified [RCV004299144]	uncertain significance	19	54158316	54158316	Human		name
401759432	CV2701549	single nucleotide variant	NM_024316.3(LENG1):c.122C>T (p.Ala41Val)	not specified [RCV004313992]	uncertain significance	19	54159574	54159574	Human		name
401872517	CV2779701	single nucleotide variant	NM_024316.3(LENG1):c.130G>C (p.Glu44Gln)	not specified [RCV004351390]	uncertain significance	19	54159566	54159566	Human		name
597640913	CV3699047	single nucleotide variant	NM_024316.3(LENG1):c.179T>C (p.Leu60Pro)	not specified [RCV004941599]	uncertain significance	19	54158415	54158415	Human		name
597640774	CV3699048	single nucleotide variant	NM_024316.3(LENG1):c.223C>G (p.Pro75Ala)	not specified [RCV004941600]	uncertain significance	19	54158371	54158371	Human		name
156067594	CV2193589	single nucleotide variant	NM_024316.3(LENG1):c.671G>A (p.Arg224Gln)	not specified [RCV004073061]	uncertain significance	19	54155845	54155845	Human		name
156139959	CV2212133	single nucleotide variant	NM_024316.3(LENG1):c.416G>C (p.Gly139Ala)	not specified [RCV004089033]	likely benign	19	54156922	54156922	Human		name
155988190	CV2234184	single nucleotide variant	NM_024316.3(LENG1):c.608G>A (p.Arg203His)	not specified [RCV004106269]	uncertain significance	19	54155908	54155908	Human		name
156232265	CV2245148	single nucleotide variant	NM_024316.3(LENG1):c.410G>A (p.Arg137Gln)	not specified [RCV004106933]	uncertain significance	19	54156928	54156928	Human		name
156188281	CV2342175	single nucleotide variant	NM_024316.3(LENG1):c.721C>T (p.Arg241Trp)	not specified [RCV004191762]	uncertain significance	19	54155795	54155795	Human		name
156186179	CV2397591	single nucleotide variant	NM_024316.3(LENG1):c.431C>G (p.Pro144Arg)	not specified [RCV004237050]	uncertain significance	19	54156907	54156907	Human		name
156002250	CV2399526	single nucleotide variant	NM_024316.3(LENG1):c.457C>T (p.Arg153Cys)	not specified [RCV004242784]	uncertain significance	19	54156881	54156881	Human		name
155931615	CV2399874	single nucleotide variant	NM_024316.3(LENG1):c.779C>T (p.Pro260Leu)	not specified [RCV004246818]	uncertain significance	19	54155737	54155737	Human		name
329391634	CV2448772	single nucleotide variant	NM_024316.3(LENG1):c.460C>G (p.Leu154Val)	not specified [RCV004261469]	uncertain significance	19	54156878	54156878	Human		name
401741592	CV2677394	single nucleotide variant	NM_024316.3(LENG1):c.715C>T (p.Arg239Trp)	not specified [RCV004289472]	uncertain significance	19	54155801	54155801	Human		name
401730693	CV2686654	single nucleotide variant	NM_024316.3(LENG1):c.607C>T (p.Arg203Cys)	not specified [RCV004300067]	uncertain significance	19	54155909	54155909	Human		name
401776842	CV2721493	single nucleotide variant	NM_024316.3(LENG1):c.386C>G (p.Pro129Arg)	not specified [RCV004316011]	uncertain significance	19	54156952	54156952	Human		name
401725171	CV2725729	single nucleotide variant	NM_024316.3(LENG1):c.778C>G (p.Pro260Ala)	not specified [RCV004322421]	uncertain significance	19	54155738	54155738	Human		name
401862957	CV2755735	single nucleotide variant	NM_024316.3(LENG1):c.658C>T (p.Arg220Trp)	not specified [RCV004342115]	uncertain significance	19	54155858	54155858	Human		name
405817858	CV3280226	single nucleotide variant	NM_024316.3(LENG1):c.472C>T (p.Arg158Trp)	not specified [RCV004412733]	uncertain significance	19	54156866	54156866	Human		name
405817857	CV3280227	single nucleotide variant	NM_024316.3(LENG1):c.514G>A (p.Gly172Ser)	not specified [RCV004412734]	uncertain significance	19	54156824	54156824	Human	1	name
405817857	CV3280227	single nucleotide variant	NM_024316.3(LENG1):c.514G>A (p.Gly172Ser)	not specified [RCV004412734]	uncertain significance	19	54156824	54156825	Human	1	name
405817856	CV3280228	single nucleotide variant	NM_024316.3(LENG1):c.702C>A (p.Asp234Glu)	not specified [RCV004412735]	likely benign	19	54155814	54155814	Human		name
405817855	CV3280229	single nucleotide variant	NM_024316.3(LENG1):c.758G>A (p.Arg253Gln)	not specified [RCV004412736]	uncertain significance	19	54155758	54155758	Human		name
407491913	CV3452695	single nucleotide variant	NM_024316.3(LENG1):c.684G>T (p.Glu228Asp)	not specified [RCV004642341]	uncertain significance	19	54155832	54155832	Human		name
597641116	CV3699044	single nucleotide variant	NM_024316.3(LENG1):c.637C>T (p.Arg213Trp)	not specified [RCV004941596]	uncertain significance	19	54155879	54155879	Human		name
597641112	CV3699045	single nucleotide variant	NM_024316.3(LENG1):c.707C>T (p.Thr236Met)	not specified [RCV004941597]	uncertain significance	19	54155809	54155809	Human		name
598236571	CV3984386	single nucleotide variant	NM_024316.3(LENG1):c.757C>T (p.Arg253Trp)	not specified [RCV005363892]	uncertain significance	19	54155759	54155759	Human		name
598236575	CV3984387	single nucleotide variant	NM_024316.3(LENG1):c.724C>T (p.Arg242Trp)	not specified [RCV005363893]	uncertain significance	19	54155792	54155792	Human		name
598198904	CV3984388	single nucleotide variant	NM_024316.3(LENG1):c.638G>A (p.Arg213Gln)	not specified [RCV005355553]	uncertain significance	19	54155878	54155878	Human		name
598236585	CV3984390	single nucleotide variant	NM_024316.3(LENG1):c.416G>T (p.Gly139Val)	not specified [RCV005363895]	uncertain significance	19	54156922	54156922	Human		name
598236589	CV3984391	single nucleotide variant	NM_024316.3(LENG1):c.559A>G (p.Lys187Glu)	not specified [RCV005363896]	uncertain significance	19	54156779	54156779	Human		name
598229858	CV3984392	single nucleotide variant	NM_024316.3(LENG1):c.763C>T (p.Pro255Ser)	not specified [RCV005362613]	uncertain significance	19	54155753	54155753	Human		name

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