Leng8 Variant Search Result - Rat Genome Database

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95 records found for search term Leng8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401929204	CV2818777	single nucleotide variant	NM_052925.4(LENG8):c.*438C>T	not provided [RCV003407114]	likely benign	19	54461366	54461366	Human		name
8637025	CV92250	single nucleotide variant	NM_052925.3(LENG8):c.*1500G>A	Malignant melanoma [RCV000072348]	not provided	19	54462428	54462428	Human		name
405277968	CV3203086	single nucleotide variant	NM_052925.4(LENG8):c.1732-9C>T	LENG8-related disorder [RCV003904772]	benign	19	54457738	54457738	Human		name , trait , alternate_id
155906944	CV2357411	single nucleotide variant	NM_052925.4(LENG8):c.26G>A (p.Arg9His)	not specified [RCV004200290]	uncertain significance	19	54451370	54451370	Human		name
405270109	CV3215355	single nucleotide variant	NM_052925.4(LENG8):c.102C>T (p.His34=)	LENG8-related disorder [RCV003949115]	likely benign	19	54452156	54452156	Human		name , trait , alternate_id
156001742	CV2391962	single nucleotide variant	NM_052925.4(LENG8):c.92C>T (p.Thr31Met)	not specified [RCV004235824]	uncertain significance	19	54452146	54452146	Human		name
405269106	CV3199214	single nucleotide variant	NM_052925.4(LENG8):c.973C>T (p.Leu325=)	LENG8-related disorder [RCV003912313]	likely benign	19	54455515	54455515	Human		name , trait , alternate_id
405289104	CV3204911	single nucleotide variant	NM_052925.4(LENG8):c.594C>T (p.Pro198=)	LENG8-related disorder [RCV003961557]	likely benign	19	54454597	54454597	Human		name , trait , alternate_id
155916285	CV2366624	single nucleotide variant	NM_052925.4(LENG8):c.224A>G (p.Gln75Arg)	not specified [RCV004210637]	uncertain significance	19	54452661	54452661	Human		name
329371693	CV2442833	single nucleotide variant	NM_052925.4(LENG8):c.191A>G (p.Asn64Ser)	not specified [RCV004253447]	uncertain significance	19	54452245	54452245	Human		name
401885078	CV2759570	single nucleotide variant	NM_052925.4(LENG8):c.169G>A (p.Gly57Ser)	not specified [RCV004338548]	likely benign	19	54452223	54452223	Human		name
401937414	CV2818776	single nucleotide variant	NM_052925.4(LENG8):c.1458G>A (p.Ala486=)	LENG8-related disorder [RCV003929106]\|not provided [RCV003415425]	likely benign	19	54456648	54456648	Human		name , trait , alternate_id
405280161	CV3191703	single nucleotide variant	NM_052925.4(LENG8):c.1935G>A (p.Thr645=)	LENG8-related disorder [RCV003919837]	likely benign	19	54458135	54458135	Human		name , trait , alternate_id
405275630	CV3199350	single nucleotide variant	NM_052925.4(LENG8):c.1848C>T (p.Arg616=)	LENG8-related disorder [RCV003916763]	likely benign	19	54457948	54457948	Human		name , trait , alternate_id
405276414	CV3206726	single nucleotide variant	NM_052925.4(LENG8):c.1890C>T (p.Ile630=)	LENG8-related disorder [RCV003917162]	benign	19	54457990	54457990	Human		name , trait , alternate_id
405271583	CV3209443	single nucleotide variant	NM_052925.4(LENG8):c.1791G>A (p.Ala597=)	LENG8-related disorder [RCV003949764]	likely benign	19	54457806	54457806	Human		name , trait , alternate_id
405288904	CV3209976	single nucleotide variant	NM_052925.4(LENG8):c.255G>C (p.Gln85His)	LENG8-related disorder [RCV003961463]	benign	19	54452692	54452692	Human		name , trait , alternate_id
405266594	CV3211905	single nucleotide variant	NM_052925.4(LENG8):c.1392C>T (p.Gly464=)	LENG8-related disorder [RCV003947179]	likely benign	19	54456412	54456412	Human		name , trait , alternate_id
405285519	CV3212556	single nucleotide variant	NM_052925.4(LENG8):c.2250T>A (p.Pro750=)	LENG8-related disorder [RCV003959131]	likely benign	19	54460775	54460775	Human		name , trait , alternate_id
405291245	CV3215320	single nucleotide variant	NM_052925.4(LENG8):c.1023G>A (p.Pro341=)	LENG8-related disorder [RCV003927405]	likely benign	19	54455565	54455565	Human		name , trait , alternate_id
405817848	CV3280236	single nucleotide variant	NM_052925.4(LENG8):c.194G>T (p.Gly65Val)	not specified [RCV004412743]	uncertain significance	19	54452248	54452248	Human		name
407491929	CV3452702	single nucleotide variant	NM_052925.4(LENG8):c.164C>T (p.Ala55Val)	not specified [RCV004642345]	uncertain significance	19	54452218	54452218	Human		name
156140782	CV2199883	single nucleotide variant	NM_052925.4(LENG8):c.559A>C (p.Thr187Pro)	not specified [RCV004074072]	uncertain significance	19	54454562	54454562	Human		name
156118456	CV2209260	single nucleotide variant	NM_052925.4(LENG8):c.725C>A (p.Pro242His)	not specified [RCV004093446]	uncertain significance	19	54454996	54454996	Human		name
156245245	CV2231663	single nucleotide variant	NM_052925.4(LENG8):c.439G>A (p.Gly147Ser)	not specified [RCV004098227]	uncertain significance	19	54454442	54454442	Human		name
156071782	CV2233320	single nucleotide variant	NM_052925.4(LENG8):c.397G>A (p.Ala133Thr)	not specified [RCV004105698]	uncertain significance	19	54453627	54453627	Human		name
156259783	CV2277863	single nucleotide variant	NM_052925.4(LENG8):c.635C>G (p.Pro212Arg)	not specified [RCV004147277]	uncertain significance	19	54454638	54454638	Human		name
155995684	CV2278115	single nucleotide variant	NM_052925.4(LENG8):c.643C>T (p.Pro215Ser)	not specified [RCV004141326]	uncertain significance	19	54454646	54454646	Human		name
155916742	CV2282241	single nucleotide variant	NM_052925.4(LENG8):c.557G>C (p.Gly186Ala)	not specified [RCV004132816]	uncertain significance	19	54454560	54454560	Human		name
156134310	CV2383125	single nucleotide variant	NM_052925.4(LENG8):c.698G>A (p.Gly233Asp)	not specified [RCV004219740]	uncertain significance	19	54454969	54454969	Human		name
329392102	CV2445316	single nucleotide variant	NM_052925.4(LENG8):c.737C>A (p.Thr246Asn)	not specified [RCV004263940]	uncertain significance	19	54455008	54455008	Human		name
401759141	CV2705403	single nucleotide variant	NM_052925.4(LENG8):c.512A>T (p.Asn171Ile)	not specified [RCV004312070]	uncertain significance	19	54454515	54454515	Human		name
405817845	CV3280239	single nucleotide variant	NM_052925.4(LENG8):c.320T>C (p.Met107Thr)	not specified [RCV004412746]	uncertain significance	19	54453550	54453550	Human		name
405817844	CV3280240	single nucleotide variant	NM_052925.4(LENG8):c.467C>T (p.Ala156Val)	not specified [RCV004412747]	uncertain significance	19	54454470	54454470	Human		name
405817843	CV3280241	single nucleotide variant	NM_052925.4(LENG8):c.595G>A (p.Ala199Thr)	not specified [RCV004412748]	uncertain significance	19	54454598	54454598	Human		name
407491917	CV3452697	single nucleotide variant	NM_052925.4(LENG8):c.770A>G (p.Gln257Arg)	not specified [RCV004642342]	uncertain significance	19	54455041	54455041	Human		name
407491925	CV3452701	single nucleotide variant	NM_052925.4(LENG8):c.631G>A (p.Glu211Lys)	not provided [RCV005242568]\|not specified [RCV004642344]	likely benign\|uncertain significance	19	54454634	54454634	Human		name
407491933	CV3452703	single nucleotide variant	NM_052925.4(LENG8):c.644C>A (p.Pro215His)	not specified [RCV004642346]	uncertain significance	19	54454647	54454647	Human		name
598229864	CV3984395	single nucleotide variant	NM_052925.4(LENG8):c.514C>T (p.Pro172Ser)	not specified [RCV005362614]	uncertain significance	19	54454517	54454517	Human		name
598198935	CV3984398	single nucleotide variant	NM_052925.4(LENG8):c.722G>T (p.Arg241Leu)	not specified [RCV005355557]	uncertain significance	19	54454993	54454993	Human		name
598236604	CV3984400	single nucleotide variant	NM_052925.4(LENG8):c.745A>G (p.Ser249Gly)	not specified [RCV005363899]	uncertain significance	19	54455016	54455016	Human		name
598198942	CV3984401	single nucleotide variant	NM_052925.4(LENG8):c.895C>T (p.Arg299Cys)	not specified [RCV005355558]	uncertain significance	19	54455437	54455437	Human		name
156327690	CV2217332	single nucleotide variant	NM_052925.4(LENG8):c.1387C>T (p.Arg463Trp)	not specified [RCV004087770]	uncertain significance	19	54456407	54456407	Human		name
156331664	CV2218198	single nucleotide variant	NM_052925.4(LENG8):c.1954G>A (p.Ala652Thr)	not specified [RCV004088403]	uncertain significance	19	54458154	54458154	Human		name
156299375	CV2244739	single nucleotide variant	NM_052925.4(LENG8):c.1066C>T (p.Arg356Trp)	not specified [RCV004102733]	uncertain significance	19	54456007	54456007	Human		name
156261868	CV2282437	single nucleotide variant	NM_052925.4(LENG8):c.2164C>T (p.Pro722Ser)	not specified [RCV004133245]	uncertain significance	19	54458445	54458445	Human		name
156005594	CV2290373	single nucleotide variant	NM_052925.4(LENG8):c.1175G>A (p.Arg392Gln)	not specified [RCV004154798]	uncertain significance	19	54456116	54456116	Human		name
156296261	CV2297552	single nucleotide variant	NM_052925.4(LENG8):c.1106C>T (p.Ala369Val)	not specified [RCV004155260]	uncertain significance	19	54456047	54456047	Human		name
156093146	CV2309908	single nucleotide variant	NM_052925.4(LENG8):c.1259G>A (p.Arg420His)	not specified [RCV004161279]	uncertain significance	19	54456200	54456200	Human		name
156054502	CV2326512	single nucleotide variant	NM_052925.4(LENG8):c.2053T>A (p.Tyr685Asn)	not specified [RCV004183068]	uncertain significance	19	54458334	54458334	Human		name
156072608	CV2331526	single nucleotide variant	NM_052925.4(LENG8):c.2387A>G (p.Gln796Arg)	not specified [RCV004182129]	uncertain significance	19	54460912	54460912	Human		name
155990410	CV2352447	single nucleotide variant	NM_052925.4(LENG8):c.2215G>C (p.Val739Leu)	not specified [RCV004202956]	uncertain significance	19	54458496	54458496	Human		name
156152856	CV2367163	single nucleotide variant	NM_052925.4(LENG8):c.1752C>G (p.Cys584Trp)	not specified [RCV004215597]	uncertain significance	19	54457767	54457767	Human		name
156063596	CV2389391	single nucleotide variant	NM_052925.4(LENG8):c.1065G>T (p.Lys355Asn)	not specified [RCV004238127]	uncertain significance	19	54456006	54456006	Human		name
156194989	CV2400445	single nucleotide variant	NM_052925.4(LENG8):c.1074G>T (p.Glu358Asp)	not specified [RCV004246651]	uncertain significance	19	54456015	54456015	Human		name
401752519	CV2682847	single nucleotide variant	NM_052925.4(LENG8):c.2348C>T (p.Pro783Leu)	not specified [RCV004283649]	uncertain significance	19	54460873	54460873	Human		name
401731840	CV2690166	single nucleotide variant	NM_052925.4(LENG8):c.1514G>A (p.Arg505Gln)	not specified [RCV004302180]	uncertain significance	19	54456704	54456704	Human		name
401725940	CV2698975	single nucleotide variant	NM_052925.4(LENG8):c.1378C>G (p.Pro460Ala)	not specified [RCV004303506]	uncertain significance	19	54456398	54456398	Human		name
401723509	CV2724927	single nucleotide variant	NM_052925.4(LENG8):c.2126G>A (p.Gly709Asp)	not specified [RCV004319695]	uncertain significance	19	54458407	54458407	Human		name
401895583	CV2778101	single nucleotide variant	NM_052925.4(LENG8):c.1565G>A (p.Arg522His)	not specified [RCV004348047]	uncertain significance	19	54456755	54456755	Human		name
405274703	CV3199766	single nucleotide variant	NM_052925.4(LENG8):c.1669A>G (p.Ile557Val)	LENG8-related disorder [RCV003973828]	benign	19	54456859	54456859	Human		name , trait , alternate_id
405266176	CV3213067	single nucleotide variant	NM_052925.4(LENG8):c.1288C>T (p.Arg430Cys)	LENG8-related disorder [RCV003969233]	benign	19	54456229	54456229	Human		name , trait , alternate_id
405817854	CV3280230	single nucleotide variant	NM_052925.4(LENG8):c.1007G>A (p.Ser336Asn)	not specified [RCV004412737]	uncertain significance	19	54455549	54455549	Human		name
405817853	CV3280231	single nucleotide variant	NM_052925.4(LENG8):c.1221C>G (p.Phe407Leu)	not specified [RCV004412738]	uncertain significance	19	54456162	54456162	Human		name
405817852	CV3280232	single nucleotide variant	NM_052925.4(LENG8):c.1237T>C (p.Ser413Pro)	not specified [RCV004412739]	uncertain significance	19	54456178	54456178	Human		name
405817851	CV3280233	single nucleotide variant	NM_052925.4(LENG8):c.1430C>T (p.Ala477Val)	not specified [RCV004412740]	uncertain significance	19	54456450	54456450	Human		name
405817850	CV3280234	single nucleotide variant	NM_052925.4(LENG8):c.1661G>T (p.Cys554Phe)	not specified [RCV004412741]	uncertain significance	19	54456851	54456851	Human		name
405817847	CV3280237	single nucleotide variant	NM_052925.4(LENG8):c.2180A>G (p.Tyr727Cys)	not specified [RCV004412744]	uncertain significance	19	54458461	54458461	Human		name
405817846	CV3280238	single nucleotide variant	NM_052925.4(LENG8):c.2309G>A (p.Arg770Gln)	not specified [RCV004412745]	uncertain significance	19	54460834	54460834	Human		name
407460597	CV3452696	single nucleotide variant	NM_052925.4(LENG8):c.2252C>T (p.Ala751Val)	not specified [RCV004633935]	uncertain significance	19	54460777	54460777	Human		name
407491921	CV3452699	single nucleotide variant	NM_052925.4(LENG8):c.2062C>G (p.Arg688Gly)	not specified [RCV004642343]	uncertain significance	19	54458343	54458343	Human		name
407460607	CV3452700	single nucleotide variant	NM_052925.4(LENG8):c.1859C>T (p.Thr620Met)	not specified [RCV004633937]	uncertain significance	19	54457959	54457959	Human		name
597640781	CV3699049	single nucleotide variant	NM_052925.4(LENG8):c.1297C>T (p.Arg433Cys)	not specified [RCV004941601]	uncertain significance	19	54456238	54456238	Human		name
597640786	CV3699051	single nucleotide variant	NM_052925.4(LENG8):c.1130G>T (p.Gly377Val)	not specified [RCV004941602]	uncertain significance	19	54456071	54456071	Human		name
597640792	CV3699052	single nucleotide variant	NM_052925.4(LENG8):c.1258C>T (p.Arg420Cys)	not specified [RCV004941603]	uncertain significance	19	54456199	54456199	Human		name
597640798	CV3699053	single nucleotide variant	NM_052925.4(LENG8):c.1112C>T (p.Ser371Leu)	not specified [RCV004941604]	uncertain significance	19	54456053	54456053	Human		name
597640803	CV3699054	single nucleotide variant	NM_052925.4(LENG8):c.2296G>A (p.Glu766Lys)	not specified [RCV004941605]	uncertain significance	19	54460821	54460821	Human		name
597795659	CV3699055	single nucleotide variant	NM_052925.4(LENG8):c.1130G>A (p.Gly377Asp)	not specified [RCV004934926]	uncertain significance	19	54456071	54456071	Human		name
597640808	CV3699056	single nucleotide variant	NM_052925.4(LENG8):c.1487C>T (p.Ala496Val)	not specified [RCV004941606]	uncertain significance	19	54456677	54456677	Human		name
597795662	CV3699057	single nucleotide variant	NM_052925.4(LENG8):c.2342C>T (p.Thr781Met)	not specified [RCV004934927]	uncertain significance	19	54460867	54460867	Human		name
597640815	CV3699058	single nucleotide variant	NM_052925.4(LENG8):c.1753A>G (p.Met585Val)	not specified [RCV004941607]	uncertain significance	19	54457768	54457768	Human		name
597795668	CV3699060	single nucleotide variant	NM_052925.4(LENG8):c.1180C>T (p.Arg394Trp)	not specified [RCV004934929]	uncertain significance	19	54456121	54456121	Human		name
597640820	CV3699061	single nucleotide variant	NM_052925.4(LENG8):c.2173T>A (p.Ser725Thr)	not specified [RCV004941608]	uncertain significance	19	54458454	54458454	Human		name
597640825	CV3699062	single nucleotide variant	NM_052925.4(LENG8):c.1147G>A (p.Gly383Arg)	not specified [RCV004941609]	uncertain significance	19	54456088	54456088	Human		name
597640831	CV3699063	single nucleotide variant	NM_052925.4(LENG8):c.1605C>A (p.Ser535Arg)	not specified [RCV004941610]	uncertain significance	19	54456795	54456795	Human		name
597640836	CV3699064	single nucleotide variant	NM_052925.4(LENG8):c.2182C>T (p.Leu728Phe)	not specified [RCV004941611]	uncertain significance	19	54458463	54458463	Human		name
597640842	CV3699065	single nucleotide variant	NM_052925.4(LENG8):c.1751G>A (p.Cys584Tyr)	not specified [RCV004941612]	uncertain significance	19	54457766	54457766	Human		name
597640847	CV3699066	single nucleotide variant	NM_052925.4(LENG8):c.2326C>G (p.Leu776Val)	not specified [RCV004941613]	uncertain significance	19	54460851	54460851	Human		name
598198912	CV3984393	single nucleotide variant	NM_052925.4(LENG8):c.1067G>A (p.Arg356Gln)	not specified [RCV005355554]	uncertain significance	19	54456008	54456008	Human		name
598198920	CV3984394	single nucleotide variant	NM_052925.4(LENG8):c.2302G>A (p.Ala768Thr)	not specified [RCV005355555]	uncertain significance	19	54460827	54460827	Human		name
598198927	CV3984396	single nucleotide variant	NM_052925.4(LENG8):c.2069T>A (p.Leu690Gln)	not specified [RCV005355556]	uncertain significance	19	54458350	54458350	Human		name
598236594	CV3984397	single nucleotide variant	NM_052925.4(LENG8):c.2063G>A (p.Arg688Gln)	not specified [RCV005363897]	uncertain significance	19	54458344	54458344	Human		name
598236609	CV3984402	single nucleotide variant	NM_052925.4(LENG8):c.1034G>A (p.Arg345Gln)	not specified [RCV005363900]	uncertain significance	19	54455975	54455975	Human		name
598236615	CV3984403	single nucleotide variant	NM_052925.4(LENG8):c.1162G>A (p.Gly388Arg)	not specified [RCV005363901]	uncertain significance	19	54456103	54456103	Human		name
8637024	CV92249	single nucleotide variant	NM_052925.3(LENG8):c.1055C>T (p.Pro352Leu)	Malignant melanoma [RCV000072347]	not provided	19	54455996	54455996	Human		name

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