Lrtm2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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39 records found for search term Lrtm2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156198968	CV2365218	single nucleotide variant	NM_001039029.3(LRTM2):c.26G>A (p.Gly9Glu)	not specified [RCV004209324]	likely benign	12	1828174	1828174	Human		name
156040145	CV2261267	single nucleotide variant	NM_001039029.3(LRTM2):c.52T>C (p.Trp18Arg)	not specified [RCV004128139]	uncertain significance	12	1828200	1828200	Human		name
156186893	CV2346655	single nucleotide variant	NM_001039029.3(LRTM2):c.44C>T (p.Ala15Val)	not specified [RCV004199680]	uncertain significance	12	1828192	1828192	Human		name
401929175	CV2810050	single nucleotide variant	NM_001039029.3(LRTM2):c.903G>A (p.Pro301=)	not provided [RCV003390147]	likely benign	12	1834511	1834511	Human		name
156168589	CV2197698	single nucleotide variant	NM_001039029.3(LRTM2):c.106C>T (p.Leu36Phe)	not specified [RCV004074904]	uncertain significance	12	1830973	1830973	Human		name
155906227	CV2393906	single nucleotide variant	NM_001039029.3(LRTM2):c.166G>A (p.Gly56Ser)	not specified [RCV004233726]	uncertain significance	12	1831033	1831033	Human		name
401719645	CV2675645	single nucleotide variant	NM_001039029.3(LRTM2):c.196G>A (p.Val66Met)	not specified [RCV004287901]	uncertain significance	12	1831063	1831063	Human		name
401720545	CV2701953	single nucleotide variant	NM_001039029.3(LRTM2):c.242G>C (p.Ser81Thr)	not specified [RCV004320553]	uncertain significance	12	1831109	1831109	Human		name
401877552	CV2790210	single nucleotide variant	NM_001039029.3(LRTM2):c.269A>C (p.Asn90Thr)	not specified [RCV004364126]	uncertain significance	12	1831136	1831136	Human		name
405810666	CV3284373	single nucleotide variant	NM_001039029.3(LRTM2):c.265G>A (p.Ala89Thr)	not specified [RCV004408101]	uncertain significance	12	1831132	1831132	Human		name
405810670	CV3284375	single nucleotide variant	NM_001039029.3(LRTM2):c.287G>A (p.Arg96Gln)	not specified [RCV004408103]	uncertain significance	12	1831154	1831154	Human		name
407480491	CV3453046	single nucleotide variant	NM_001039029.3(LRTM2):c.212G>A (p.Arg71Gln)	not specified [RCV004636283]	uncertain significance	12	1831079	1831079	Human		name
407481044	CV3453048	single nucleotide variant	NM_001039029.3(LRTM2):c.102G>T (p.Glu34Asp)	not specified [RCV004640140]	uncertain significance	12	1830969	1830969	Human		name
597634869	CV3702487	single nucleotide variant	NM_001039029.3(LRTM2):c.244G>A (p.Ala82Thr)	not specified [RCV004940481]	uncertain significance	12	1831111	1831111	Human		name
597634880	CV3702489	single nucleotide variant	NM_001039029.3(LRTM2):c.199C>G (p.Pro67Ala)	not specified [RCV004940483]	uncertain significance	12	1831066	1831066	Human		name
598223625	CV3985038	single nucleotide variant	NM_001039029.3(LRTM2):c.202G>C (p.Ala68Pro)	not specified [RCV005380078]	uncertain significance	12	1831069	1831069	Human		name
156237589	CV2265211	single nucleotide variant	NM_001039029.3(LRTM2):c.484G>A (p.Gly162Arg)	not specified [RCV004126328]	uncertain significance	12	1831351	1831351	Human		name
155966685	CV2280101	single nucleotide variant	NM_001039029.3(LRTM2):c.445A>C (p.Ile149Leu)	not specified [RCV004146756]	uncertain significance	12	1831312	1831312	Human		name
156354995	CV2324392	single nucleotide variant	NM_001039029.3(LRTM2):c.396C>A (p.Asp132Glu)	not specified [RCV004178889]	uncertain significance	12	1831263	1831263	Human		name
156050046	CV2378366	single nucleotide variant	NM_001039029.3(LRTM2):c.491T>C (p.Leu164Pro)	not specified [RCV004226389]	likely benign	12	1831358	1831358	Human		name
156391218	CV2385179	single nucleotide variant	NM_001039029.3(LRTM2):c.349A>G (p.Asn117Asp)	not specified [RCV004228431]	uncertain significance	12	1831216	1831216	Human		name
401748271	CV2696578	single nucleotide variant	NM_001039029.3(LRTM2):c.898C>T (p.Arg300Trp)	not specified [RCV004312619]	uncertain significance	12	1834506	1834506	Human		name
401781190	CV2732318	single nucleotide variant	NM_001039029.3(LRTM2):c.905C>A (p.Ala302Glu)	not specified [RCV004331490]	uncertain significance	12	1834513	1834513	Human		name
401778828	CV2732912	single nucleotide variant	NM_001039029.3(LRTM2):c.542G>A (p.Arg181Gln)	not specified [RCV004331091]	uncertain significance	12	1831409	1831409	Human		name
401862749	CV2758891	single nucleotide variant	NM_001039029.3(LRTM2):c.844G>A (p.Gly282Arg)	not specified [RCV004339975]	uncertain significance	12	1834452	1834452	Human		name
405810672	CV3284376	single nucleotide variant	NM_001039029.3(LRTM2):c.402C>A (p.Asp134Glu)	not specified [RCV004408104]	uncertain significance	12	1831269	1831269	Human		name
405810674	CV3284377	single nucleotide variant	NM_001039029.3(LRTM2):c.409C>T (p.Arg137Trp)	not specified [RCV004408105]	uncertain significance	12	1831276	1831276	Human		name
405810676	CV3284378	single nucleotide variant	NM_001039029.3(LRTM2):c.451G>A (p.Gly151Ser)	not specified [RCV004408106]	uncertain significance	12	1831318	1831318	Human		name
405810678	CV3284379	single nucleotide variant	NM_001039029.3(LRTM2):c.509C>G (p.Ser170Trp)	not specified [RCV004408107]	uncertain significance	12	1831376	1831376	Human		name
407481033	CV3453045	single nucleotide variant	NM_001039029.3(LRTM2):c.317G>A (p.Arg106Gln)	not specified [RCV004640138]	likely benign	12	1831184	1831184	Human		name
407481039	CV3453047	single nucleotide variant	NM_001039029.3(LRTM2):c.955G>A (p.Gly319Ser)	not specified [RCV004640139]	uncertain significance	12	1834563	1834563	Human		name
407481051	CV3453049	single nucleotide variant	NM_001039029.3(LRTM2):c.419C>G (p.Pro140Arg)	not specified [RCV004640141]	uncertain significance	12	1831286	1831286	Human		name
597634859	CV3702485	single nucleotide variant	NM_001039029.3(LRTM2):c.574C>A (p.Leu192Met)	not specified [RCV004940479]	uncertain significance	12	1831441	1831441	Human		name
597634864	CV3702486	single nucleotide variant	NM_001039029.3(LRTM2):c.664C>T (p.Arg222Cys)	not specified [RCV004940480]	uncertain significance	12	1834272	1834272	Human		name
597634874	CV3702488	single nucleotide variant	NM_001039029.3(LRTM2):c.829G>A (p.Ala277Thr)	not specified [RCV004940482]	uncertain significance	12	1834437	1834437	Human		name
598252987	CV3985039	single nucleotide variant	NM_001039029.3(LRTM2):c.763G>A (p.Asp255Asn)	not specified [RCV005366752]	uncertain significance	12	1834371	1834371	Human		name
155919325	CV2360226	single nucleotide variant	NM_001039029.3(LRTM2):c.1081G>C (p.Glu361Gln)	not specified [RCV004208574]	uncertain significance	12	1834689	1834689	Human		name
597634852	CV3702484	single nucleotide variant	NM_001039029.3(LRTM2):c.1066C>A (p.Pro356Thr)	not specified [RCV004940478]	uncertain significance	12	1834674	1834674	Human		name
8634600	CV89820	single nucleotide variant	NM_001039029.2(LRTM2):c.1108G>A (p.Ala370Thr)	Malignant melanoma [RCV000069917]	not provided	12	1834716	1834716	Human		name

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