Lpar1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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27 records found for search term Lpar1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8650975	CV127550	single nucleotide variant	NM_001401.3(LPAR1):c.794-10956T>C	Lung cancer [RCV000108037]	uncertain significance	9	110886678	110886678	Human		name
598261571	CV3991861	single nucleotide variant	NM_001351411.2(LPAR1):c.5C>A (p.Ala2Asp)	not specified [RCV005347868]	uncertain significance	9	110972113	110972113	Human		name
8633187	CV88400	single nucleotide variant	NM_001401.3(LPAR1):c.236G>A (p.Arg79His)	Malignant melanoma [RCV000068492]	not provided	9	110941978	110941978	Human		name
156047142	CV2315667	single nucleotide variant	NM_001351411.2(LPAR1):c.13T>C (p.Ser5Pro)	not specified [RCV004169695]	uncertain significance	9	110972105	110972105	Human		name
405815511	CV3284123	single nucleotide variant	NM_001351411.2(LPAR1):c.59A>G (p.Asn20Ser)	not specified [RCV004410520]	uncertain significance	9	110942155	110942155	Human		name
407471413	CV3445932	single nucleotide variant	NM_001351411.2(LPAR1):c.82G>A (p.Glu28Lys)	not specified [RCV004637393]	uncertain significance	9	110942132	110942132	Human		name
598261583	CV3991863	single nucleotide variant	NM_001351411.2(LPAR1):c.71G>C (p.Cys24Ser)	not specified [RCV005347870]	uncertain significance	9	110942143	110942143	Human		name
15173147	CV706394	single nucleotide variant	NM_001351411.2(LPAR1):c.435G>A (p.Glu145=)	not provided [RCV000950178]	benign	9	110941779	110941779	Human		name
156136488	CV2357188	single nucleotide variant	NM_001351411.2(LPAR1):c.232C>T (p.Arg78Cys)	not specified [RCV004206974]	uncertain significance	9	110941982	110941982	Human		name
405815509	CV3284121	single nucleotide variant	NM_001351411.2(LPAR1):c.181A>G (p.Ile61Val)	not specified [RCV004410518]	uncertain significance	9	110942033	110942033	Human		name
405815510	CV3284122	single nucleotide variant	NM_001351411.2(LPAR1):c.241C>T (p.His81Tyr)	not specified [RCV004410519]	uncertain significance	9	110941973	110941973	Human		name
597623437	CV3702022	single nucleotide variant	NM_001351411.2(LPAR1):c.110G>A (p.Ser37Asn)	not specified [RCV004936464]	uncertain significance	9	110942104	110942104	Human		name
598261578	CV3991862	single nucleotide variant	NM_001351411.2(LPAR1):c.128C>G (p.Thr43Arg)	not specified [RCV005347869]	uncertain significance	9	110942086	110942086	Human		name
156238256	CV2193624	single nucleotide variant	NM_001351411.2(LPAR1):c.781G>A (p.Val261Ile)	not specified [RCV004074229]	uncertain significance	9	110941433	110941433	Human		name
156239306	CV2235907	single nucleotide variant	NM_001351411.2(LPAR1):c.317T>C (p.Met106Thr)	not specified [RCV004113799]	uncertain significance	9	110941897	110941897	Human		name
156136738	CV2257171	single nucleotide variant	NM_001351411.2(LPAR1):c.509T>C (p.Val170Ala)	not specified [RCV004123123]	uncertain significance	9	110941705	110941705	Human		name
156249629	CV2314172	single nucleotide variant	NM_001351411.2(LPAR1):c.730T>A (p.Ser244Thr)	not specified [RCV004166254]	uncertain significance	9	110941484	110941484	Human		name
156249647	CV2314173	single nucleotide variant	NM_001351411.2(LPAR1):c.731C>T (p.Ser244Phe)	not specified [RCV004166255]	uncertain significance	9	110941483	110941483	Human		name
156178717	CV2327608	single nucleotide variant	NM_001351411.2(LPAR1):c.914C>T (p.Ala305Val)	not specified [RCV004177193]	uncertain significance	9	110875602	110875602	Human		name
405866908	CV2842421	single nucleotide variant	NM_001351411.2(LPAR1):c.454C>T (p.Arg152Cys)	EBV-positive nodal T- and NK-cell lymphoma [RCV004557778]	likely benign	9	110941760	110941760	Human		name
405815512	CV3284124	single nucleotide variant	NM_001351411.2(LPAR1):c.845T>C (p.Val282Ala)	not specified [RCV004410521]	uncertain significance	9	110875671	110875671	Human		name
407471407	CV3445931	single nucleotide variant	NM_001351411.2(LPAR1):c.520A>G (p.Met174Val)	not specified [RCV004637392]	uncertain significance	9	110941694	110941694	Human		name
597623436	CV3702021	single nucleotide variant	NM_001351411.2(LPAR1):c.529G>A (p.Val177Ile)	not specified [RCV004936463]	uncertain significance	9	110941685	110941685	Human		name
598261588	CV3991864	single nucleotide variant	NM_001351411.2(LPAR1):c.334A>G (p.Asn112Asp)	not specified [RCV005347871]	uncertain significance	9	110941880	110941880	Human		name
156043147	CV2311026	single nucleotide variant	NM_001351411.2(LPAR1):c.1006G>A (p.Gly336Ser)	not specified [RCV004164043]	uncertain significance	9	110875510	110875510	Human		name
405815508	CV3284120	single nucleotide variant	NM_001351411.2(LPAR1):c.1031C>T (p.Ser344Leu)	not specified [RCV004410517]	uncertain significance	9	110875485	110875485	Human		name
598238816	CV3991860	single nucleotide variant	NM_001351411.2(LPAR1):c.1028G>A (p.Arg343His)	not specified [RCV005364319]	uncertain significance	9	110875488	110875488	Human		name

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