Gnl3l Variant Search Result - Rat Genome Database

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58 records found for search term Gnl3l

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156134475	CV2260152	single nucleotide variant	NM_001184819.2(GNL3L):c.37G>A (p.Glu13Lys)	not specified [RCV004119144]	likely benign	X	54539057	54539057	Human		name
156311293	CV2260153	single nucleotide variant	NM_001184819.2(GNL3L):c.44C>A (p.Ser15Tyr)	not specified [RCV004119145]	uncertain significance	X	54539064	54539064	Human		name
156005963	CV2394093	single nucleotide variant	NM_001184819.2(GNL3L):c.41G>A (p.Gly14Asp)	not specified [RCV004236302]	uncertain significance	X	54539061	54539061	Human		name
401918950	CV2829062	single nucleotide variant	NM_001184819.2(GNL3L):c.351C>T (p.Asp117=)	not provided [RCV003430513]	likely benign	X	54542999	54542999	Human		name
401918953	CV2829063	single nucleotide variant	NM_001184819.2(GNL3L):c.972C>T (p.His324=)	not provided [RCV003430514]	likely benign	X	54551676	54551676	Human		name
156369044	CV2263253	single nucleotide variant	NM_001184819.2(GNL3L):c.196G>A (p.Glu66Lys)	not specified [RCV004131752]	uncertain significance	X	54541279	54541279	Human		name
329354854	CV2449127	single nucleotide variant	NM_001184819.2(GNL3L):c.253A>G (p.Ile85Val)	not specified [RCV004264188]	uncertain significance	X	54541336	54541336	Human		name
401750628	CV2715709	single nucleotide variant	NM_001184819.2(GNL3L):c.172G>C (p.Glu58Gln)	not specified [RCV004328858]	uncertain significance	X	54540225	54540225	Human		name
401918949	CV2829061	single nucleotide variant	NM_001184819.2(GNL3L):c.122C>T (p.Pro41Leu)	not provided [RCV003430512]	likely benign	X	54540175	54540175	Human		name
407520074	CV3439667	single nucleotide variant	NM_001184819.2(GNL3L):c.153T>G (p.Asp51Glu)	not specified [RCV004629918]	uncertain significance	X	54540206	54540206	Human		name
596948312	CV3549394	single nucleotide variant	NM_001184819.2(GNL3L):c.283C>T (p.Arg95Cys)	not provided [RCV004812214]	likely benign	X	54541366	54541366	Human		name
598264246	CV3974408	single nucleotide variant	NM_001184819.2(GNL3L):c.259A>G (p.Ser87Gly)	not specified [RCV005348811]	uncertain significance	X	54541342	54541342	Human		name
156108908	CV2211084	single nucleotide variant	NM_001184819.2(GNL3L):c.733C>T (p.Arg245Cys)	not specified [RCV004088263]	uncertain significance	X	54548331	54548331	Human		name
156158422	CV2236094	single nucleotide variant	NM_001184819.2(GNL3L):c.986C>T (p.Ala329Val)	not specified [RCV004114246]	uncertain significance	X	54551690	54551690	Human		name
156086280	CV2289936	single nucleotide variant	NM_001184819.2(GNL3L):c.412A>G (p.Ile138Val)	not specified [RCV004150587]	uncertain significance	X	54543228	54543228	Human		name
156045355	CV2308075	single nucleotide variant	NM_001184819.2(GNL3L):c.785A>G (p.Asn262Ser)	not specified [RCV004170499]	uncertain significance	X	54550972	54550972	Human		name
155972532	CV2335810	single nucleotide variant	NM_001184819.2(GNL3L):c.967G>A (p.Val323Ile)	not specified [RCV004196045]	likely benign	X	54551671	54551671	Human		name
156142400	CV2383773	single nucleotide variant	NM_001184819.2(GNL3L):c.959G>A (p.Arg320His)	not specified [RCV004231651]	uncertain significance	X	54551663	54551663	Human		name
329395263	CV2458250	single nucleotide variant	NM_001184819.2(GNL3L):c.538A>G (p.Lys180Glu)	not specified [RCV004265906]	uncertain significance	X	54544234	54544234	Human		name
401773106	CV2698095	single nucleotide variant	NM_001184819.2(GNL3L):c.352G>A (p.Glu118Lys)	not specified [RCV004302888]	uncertain significance	X	54543000	54543000	Human		name
401861784	CV2756686	single nucleotide variant	NM_001184819.2(GNL3L):c.787G>A (p.Val263Ile)	not specified [RCV004345197]	uncertain significance	X	54550974	54550974	Human		name
401858093	CV2759582	single nucleotide variant	NM_001184819.2(GNL3L):c.481C>G (p.Arg161Gly)	not specified [RCV004338558]	uncertain significance	X	54543297	54543297	Human		name
405768663	CV3262143	single nucleotide variant	NM_001184819.2(GNL3L):c.544G>A (p.Val182Ile)	not specified [RCV004395533]	uncertain significance	X	54544240	54544240	Human		name
405768667	CV3262144	single nucleotide variant	NM_001184819.2(GNL3L):c.635G>A (p.Arg212His)	not specified [RCV004395534]	uncertain significance	X	54548233	54548233	Human		name
405768673	CV3262145	single nucleotide variant	NM_001184819.2(GNL3L):c.746T>C (p.Val249Ala)	not specified [RCV004395535]	uncertain significance	X	54548344	54548344	Human		name
597788515	CV3678282	single nucleotide variant	NM_001184819.2(GNL3L):c.973G>A (p.Val325Met)	not specified [RCV004932762]	uncertain significance	X	54551677	54551677	Human		name
597730667	CV3678285	single nucleotide variant	NM_001184819.2(GNL3L):c.638G>C (p.Cys213Ser)	not specified [RCV004919843]	uncertain significance	X	54548236	54548236	Human		name
597788528	CV3678288	single nucleotide variant	NM_001184819.2(GNL3L):c.497A>G (p.Lys166Arg)	not specified [RCV004932765]	uncertain significance	X	54543313	54543313	Human		name
597730692	CV3678290	single nucleotide variant	NM_001184819.2(GNL3L):c.835A>C (p.Ser279Arg)	not specified [RCV004919845]	uncertain significance	X	54551022	54551022	Human		name
598264231	CV3974405	single nucleotide variant	NM_001184819.2(GNL3L):c.581T>C (p.Leu194Ser)	not specified [RCV005348808]	uncertain significance	X	54544277	54544277	Human		name
598232799	CV3974409	single nucleotide variant	NM_001184819.2(GNL3L):c.899G>T (p.Arg300Leu)	not specified [RCV005342656]	uncertain significance	X	54551603	54551603	Human		name
598232806	CV3974410	single nucleotide variant	NM_001184819.2(GNL3L):c.329A>C (p.Asn110Thr)	not specified [RCV005342657]	uncertain significance	X	54542977	54542977	Human		name
156047237	CV2216139	single nucleotide variant	NM_001184819.2(GNL3L):c.1391A>G (p.His464Arg)	not specified [RCV004097138]	uncertain significance	X	54554637	54554637	Human		name
156074954	CV2230099	single nucleotide variant	NM_001184819.2(GNL3L):c.1300A>G (p.Asn434Asp)	not specified [RCV004099751]	uncertain significance	X	54552410	54552410	Human		name
155988127	CV2234176	single nucleotide variant	NM_001184819.2(GNL3L):c.1520A>G (p.His507Arg)	not specified [RCV004106262]	uncertain significance	X	54558509	54558509	Human		name
156202824	CV2234542	single nucleotide variant	NM_001184819.2(GNL3L):c.1505A>C (p.Lys502Thr)	not specified [RCV004100735]	uncertain significance	X	54558494	54558494	Human		name
155914896	CV2242863	single nucleotide variant	NM_001184819.2(GNL3L):c.1475A>G (p.Asn492Ser)	not specified [RCV004107454]	uncertain significance	X	54558464	54558464	Human		name
156088897	CV2259083	single nucleotide variant	NM_001184819.2(GNL3L):c.1121A>G (p.Lys374Arg)	not specified [RCV004120341]	uncertain significance	X	54551914	54551914	Human		name
156078945	CV2300869	single nucleotide variant	NM_001184819.2(GNL3L):c.1642A>G (p.Lys548Glu)	not specified [RCV004158072]	uncertain significance	X	54558631	54558631	Human		name
156260710	CV2322320	single nucleotide variant	NM_001184819.2(GNL3L):c.1192A>G (p.Ser398Gly)	not specified [RCV004176079]	uncertain significance	X	54552302	54552302	Human		name
156003056	CV2347749	single nucleotide variant	NM_001184819.2(GNL3L):c.1255A>G (p.Lys419Glu)	not specified [RCV004202715]	uncertain significance	X	54552365	54552365	Human		name
156064882	CV2348676	single nucleotide variant	NM_001184819.2(GNL3L):c.1501G>T (p.Ala501Ser)	not specified [RCV004201092]	uncertain significance	X	54558490	54558490	Human		name
156139548	CV2374311	single nucleotide variant	NM_001184819.2(GNL3L):c.1724A>G (p.Asn575Ser)	not specified [RCV004229442]	uncertain significance	X	54560577	54560577	Human		name
401730159	CV2680018	single nucleotide variant	NM_001184819.2(GNL3L):c.1403C>T (p.Thr468Met)	not specified [RCV004286522]	likely benign	X	54554649	54554649	Human		name
401731451	CV2701373	single nucleotide variant	NM_001184819.2(GNL3L):c.1135T>C (p.Tyr379His)	not specified [RCV004311741]	uncertain significance	X	54551928	54551928	Human		name
401871007	CV2756568	single nucleotide variant	NM_001184819.2(GNL3L):c.1523G>A (p.Arg508His)	not specified [RCV004345093]	likely benign	X	54558512	54558512	Human		name
401872690	CV2793142	single nucleotide variant	NM_001184819.2(GNL3L):c.1522C>T (p.Arg508Cys)	not specified [RCV004360451]	likely benign	X	54558511	54558511	Human		name
405768645	CV3262140	single nucleotide variant	NM_001184819.2(GNL3L):c.1310C>T (p.Thr437Ile)	not specified [RCV004395530]	uncertain significance	X	54552420	54552420	Human		name
405768651	CV3262141	single nucleotide variant	NM_001184819.2(GNL3L):c.1595C>T (p.Thr532Met)	not specified [RCV004395531]	uncertain significance	X	54558584	54558584	Human		name
405768657	CV3262142	single nucleotide variant	NM_001184819.2(GNL3L):c.1649A>T (p.Lys550Met)	not specified [RCV004395532]	uncertain significance	X	54558638	54558638	Human		name
597730643	CV3678283	single nucleotide variant	NM_001184819.2(GNL3L):c.1576C>A (p.Leu526Met)	not specified [RCV004919841]	uncertain significance	X	54558565	54558565	Human		name
597730655	CV3678284	single nucleotide variant	NM_001184819.2(GNL3L):c.1428T>G (p.Asn476Lys)	not specified [RCV004919842]	uncertain significance	X	54554674	54554674	Human		name
597788519	CV3678286	single nucleotide variant	NM_001184819.2(GNL3L):c.1009A>G (p.Thr337Ala)	not specified [RCV004932763]	uncertain significance	X	54551713	54551713	Human		name
597788524	CV3678287	single nucleotide variant	NM_001184819.2(GNL3L):c.1267G>A (p.Glu423Lys)	not specified [RCV004932764]	uncertain significance	X	54552377	54552377	Human		name
597730679	CV3678289	single nucleotide variant	NM_001184819.2(GNL3L):c.1471A>G (p.Thr491Ala)	not specified [RCV004919844]	uncertain significance	X	54558460	54558460	Human		name
598264236	CV3974406	single nucleotide variant	NM_001184819.2(GNL3L):c.1564C>T (p.Arg522Cys)	not specified [RCV005348809]	uncertain significance	X	54558553	54558553	Human		name
598264241	CV3974407	single nucleotide variant	NM_001184819.2(GNL3L):c.1547A>T (p.Asp516Val)	not specified [RCV005348810]	uncertain significance	X	54558536	54558536	Human		name
15185883	CV706280	deletion	NM_001184819.2(GNL3L):c.177_179del (p.Lys62del)	not provided [RCV000953116]	benign	X	54540230	54540232	Human		name

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