Lmln Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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49 records found for search term Lmln

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15113885	CV730205	single nucleotide variant	NM_001136049.3(LMLN):c.196-9T>A	not provided [RCV000894755]	benign	3	197974368	197974368	Human		name
15128266	CV744052	single nucleotide variant	NM_001136049.3(LMLN):c.407+7C>G	not provided [RCV000897241]	benign	3	197976118	197976118	Human		name
156368337	CV2199823	single nucleotide variant	NM_001136049.3(LMLN):c.64C>G (p.Arg22Gly)	not specified [RCV004074021]	uncertain significance	3	197960309	197960309	Human		name
155954223	CV2303310	single nucleotide variant	NM_001136049.3(LMLN):c.64C>T (p.Arg22Cys)	not specified [RCV004159057]	uncertain significance	3	197960309	197960309	Human		name
156064109	CV2316051	single nucleotide variant	NM_001136049.3(LMLN):c.74G>C (p.Gly25Ala)	not specified [RCV004165929]	uncertain significance	3	197960319	197960319	Human		name
156076811	CV2375062	single nucleotide variant	NM_001136049.3(LMLN):c.50G>A (p.Gly17Asp)	not specified [RCV004230110]	uncertain significance	3	197960295	197960295	Human		name
598238045	CV3981062	single nucleotide variant	NM_001136049.3(LMLN):c.63G>T (p.Trp21Cys)	not specified [RCV005364187]	uncertain significance	3	197960308	197960308	Human		name
598238057	CV3981067	single nucleotide variant	NM_001136049.3(LMLN):c.69G>C (p.Trp23Cys)	not specified [RCV005364189]	uncertain significance	3	197960314	197960314	Human		name
598261131	CV3981069	single nucleotide variant	NM_001136049.3(LMLN):c.46C>G (p.Pro16Ala)	not specified [RCV005347774]	uncertain significance	3	197960291	197960291	Human		name
598238065	CV3981070	single nucleotide variant	NM_001136049.3(LMLN):c.79G>A (p.Val27Met)	not specified [RCV005364190]	likely benign	3	197960324	197960324	Human		name
8625594	CV80718	single nucleotide variant	NM_001136049.2(LMLN):c.399C>T (p.Val133=)	Malignant melanoma [RCV000060795]	not provided	3	197976079	197976079	Human		name
329395145	CV2458163	single nucleotide variant	NM_001136049.3(LMLN):c.163C>T (p.Pro55Ser)	not specified [RCV004265835]	uncertain significance	3	197960408	197960408	Human		name
407470933	CV3449245	single nucleotide variant	NM_001136049.3(LMLN):c.213T>G (p.His71Gln)	not specified [RCV004637243]	uncertain significance	3	197974394	197974394	Human		name
597623187	CV3693355	single nucleotide variant	NM_001136049.3(LMLN):c.203A>G (p.Asn68Ser)	not specified [RCV004936220]	uncertain significance	3	197974384	197974384	Human		name
597623191	CV3693363	single nucleotide variant	NM_001136049.3(LMLN):c.124A>G (p.Ser42Gly)	not specified [RCV004936224]	uncertain significance	3	197960369	197960369	Human		name
597795928	CV3693365	single nucleotide variant	NM_001136049.3(LMLN):c.118C>T (p.Arg40Trp)	not specified [RCV004935042]	uncertain significance	3	197960363	197960363	Human		name
15184082	CV708772	single nucleotide variant	NM_001136049.3(LMLN):c.1056T>A (p.Val352=)	not provided [RCV000975027]	benign	3	197996207	197996207	Human		name
15145966	CV748176	single nucleotide variant	NM_001136049.3(LMLN):c.1044T>C (p.Phe348=)	not provided [RCV000922635]	likely benign	3	197996195	197996195	Human		name
155973741	CV2211090	single nucleotide variant	NM_001136049.3(LMLN):c.380G>A (p.Arg127Gln)	not specified [RCV004088269]	uncertain significance	3	197976084	197976084	Human		name
155950830	CV2267915	single nucleotide variant	NM_001136049.3(LMLN):c.719A>T (p.Tyr240Phe)	not specified [RCV004136206]	uncertain significance	3	197983957	197983957	Human		name
329394233	CV2472394	single nucleotide variant	NM_001136049.3(LMLN):c.709A>G (p.Ile237Val)	not specified [RCV004285268]	uncertain significance	3	197983947	197983947	Human		name
405809661	CV3287687	single nucleotide variant	NM_001136049.3(LMLN):c.433C>T (p.Arg145Trp)	not specified [RCV004407649]	uncertain significance	3	197976623	197976623	Human		name
405809663	CV3287688	single nucleotide variant	NM_001136049.3(LMLN):c.515A>G (p.Glu172Gly)	not specified [RCV004407650]	uncertain significance	3	197976705	197976705	Human		name
405809665	CV3287689	single nucleotide variant	NM_001136049.3(LMLN):c.968G>A (p.Arg323Gln)	not specified [RCV004407651]	uncertain significance	3	197990621	197990621	Human		name
407470920	CV3449242	single nucleotide variant	NM_001136049.3(LMLN):c.502A>G (p.Ile168Val)	not specified [RCV004637240]	likely benign	3	197976692	197976692	Human		name
407470929	CV3449244	single nucleotide variant	NM_001136049.3(LMLN):c.392C>T (p.Thr131Ile)	not specified [RCV004637242]	uncertain significance	3	197976096	197976096	Human		name
597795918	CV3693356	single nucleotide variant	NM_001136049.3(LMLN):c.329A>T (p.Lys110Met)	not specified [RCV004935039]	uncertain significance	3	197976033	197976033	Human		name
597623188	CV3693358	single nucleotide variant	NM_001136049.3(LMLN):c.344C>T (p.Ala115Val)	not specified [RCV004936221]	uncertain significance	3	197976048	197976048	Human		name
597796219	CV3693362	single nucleotide variant	NM_001136049.3(LMLN):c.637G>A (p.Glu213Lys)	not specified [RCV004935041]	uncertain significance	3	197980437	197980437	Human		name
598261121	CV3981065	single nucleotide variant	NM_001136049.3(LMLN):c.548G>T (p.Gly183Val)	not specified [RCV005347772]	uncertain significance	3	197980348	197980348	Human		name
9686843	CV171363	single nucleotide variant	NM_001136049.3(LMLN):c.1093G>T (p.Gly365Cys)	Prostate cancer [RCV000149061]	uncertain significance	3	197996244	197996244	Human	2	name
156230934	CV2199617	single nucleotide variant	NM_001136049.3(LMLN):c.1787C>G (p.Thr596Ser)	not specified [RCV004072363]	uncertain significance	3	198035876	198035876	Human		name
156064606	CV2228997	single nucleotide variant	NM_001136049.3(LMLN):c.1942G>A (p.Ala648Thr)	not specified [RCV004098783]	uncertain significance	3	198036031	198036031	Human		name
156208687	CV2250140	single nucleotide variant	NM_001136049.3(LMLN):c.1823C>G (p.Pro608Arg)	not specified [RCV004116948]	uncertain significance	3	198035912	198035912	Human		name
156070409	CV2267162	single nucleotide variant	NM_001136049.3(LMLN):c.1967G>C (p.Cys656Ser)	not specified [RCV004133851]	uncertain significance	3	198038579	198038579	Human		name
329391734	CV2453077	single nucleotide variant	NM_001136049.3(LMLN):c.1177C>G (p.Arg393Gly)	not specified [RCV004277685]	uncertain significance	3	197999311	197999311	Human		name
405809647	CV3287681	single nucleotide variant	NM_001136049.3(LMLN):c.1106A>G (p.Asn369Ser)	not specified [RCV004407643]	uncertain significance	3	197996257	197996257	Human		name
405809650	CV3287682	single nucleotide variant	NM_001136049.3(LMLN):c.1196T>C (p.Met399Thr)	not specified [RCV004407644]	uncertain significance	3	197999330	197999330	Human		name
405809652	CV3287683	single nucleotide variant	NM_001136049.3(LMLN):c.1267T>G (p.Cys423Gly)	not specified [RCV004407645]	uncertain significance	3	198003073	198003073	Human		name
405809654	CV3287684	single nucleotide variant	NM_001136049.3(LMLN):c.1657G>A (p.Val553Ile)	not specified [RCV004407646]	uncertain significance	3	198024702	198024702	Human		name
405809656	CV3287685	single nucleotide variant	NM_001136049.3(LMLN):c.1856A>T (p.Asp619Val)	not specified [RCV004407647]	uncertain significance	3	198035945	198035945	Human		name
405809659	CV3287686	single nucleotide variant	NM_001136049.3(LMLN):c.1940G>A (p.Arg647Gln)	not specified [RCV004407648]	uncertain significance	3	198036029	198036029	Human		name
597795921	CV3693357	single nucleotide variant	NM_001136049.3(LMLN):c.1958T>C (p.Leu653Pro)	not specified [RCV004935040]	uncertain significance	3	198038570	198038570	Human		name
597623189	CV3693359	single nucleotide variant	NM_001136049.3(LMLN):c.1757C>G (p.Pro586Arg)	not specified [RCV004936222]	uncertain significance	3	198035846	198035846	Human		name
597623190	CV3693361	single nucleotide variant	NM_001136049.3(LMLN):c.1693A>C (p.Lys565Gln)	not specified [RCV004936223]	uncertain significance	3	198024738	198024738	Human		name
597623192	CV3693364	single nucleotide variant	NM_001136049.3(LMLN):c.1062G>C (p.Glu354Asp)	not specified [RCV004936225]	uncertain significance	3	197996213	197996213	Human		name
598238051	CV3981063	single nucleotide variant	NM_001136049.3(LMLN):c.1855G>A (p.Asp619Asn)	not specified [RCV005364188]	uncertain significance	3	198035944	198035944	Human		name
598230516	CV3981066	single nucleotide variant	NM_001136049.3(LMLN):c.1777G>A (p.Val593Ile)	not specified [RCV005362719]	uncertain significance	3	198035866	198035866	Human		name
598261126	CV3981068	single nucleotide variant	NM_001136049.3(LMLN):c.1255C>G (p.Arg419Gly)	not specified [RCV005347773]	uncertain significance	3	198003061	198003061	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

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InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

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