Gpr87 Variant Search Result - Rat Genome Database

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38 records found for search term Gpr87

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598128797	CV3886595	single nucleotide variant	NM_023915.4(GPR87):c.35-17C>T	not provided [RCV005244255]	benign	3	151295228	151295228	Human		name
156154442	CV2328651	single nucleotide variant	NM_023915.4(GPR87):c.4G>A (p.Gly2Arg)	not specified [RCV004177897]	uncertain significance	3	151300097	151300097	Human		name
597745565	CV3681659	single nucleotide variant	NM_023915.4(GPR87):c.17C>T (p.Thr6Met)	not specified [RCV004922502]	uncertain significance	3	151300084	151300084	Human		name
156066949	CV2323992	single nucleotide variant	NM_023915.4(GPR87):c.82G>A (p.Asp28Asn)	not specified [RCV004176508]	uncertain significance	3	151295164	151295164	Human		name
401890795	CV2772172	single nucleotide variant	NM_023915.4(GPR87):c.86G>C (p.Gly29Ala)	not specified [RCV004346821]	uncertain significance	3	151295160	151295160	Human		name
405740236	CV3252142	single nucleotide variant	NM_023915.4(GPR87):c.76A>G (p.Arg26Gly)	not specified [RCV004391226]	uncertain significance	3	151295170	151295170	Human		name
597769811	CV3681661	single nucleotide variant	NM_023915.4(GPR87):c.36T>A (p.Asn12Lys)	not specified [RCV004928173]	uncertain significance	3	151295210	151295210	Human		name
598274718	CV3967406	single nucleotide variant	NM_023915.4(GPR87):c.40G>A (p.Glu14Lys)	not specified [RCV005351549]	uncertain significance	3	151295206	151295206	Human		name
156399631	CV2202118	single nucleotide variant	NM_023915.4(GPR87):c.125C>T (p.Thr42Ile)	not specified [RCV004078072]	uncertain significance	3	151295121	151295121	Human		name
156243604	CV2242944	single nucleotide variant	NM_023915.4(GPR87):c.142C>T (p.Leu48Phe)	not specified [RCV004107829]	uncertain significance	3	151295104	151295104	Human		name
155984765	CV2247793	single nucleotide variant	NM_023915.4(GPR87):c.112A>G (p.Asn38Asp)	not specified [RCV004121260]	uncertain significance	3	151295134	151295134	Human		name
597769816	CV3681662	single nucleotide variant	NM_023915.4(GPR87):c.127A>G (p.Ile43Val)	not specified [RCV004928174]	uncertain significance	3	151295119	151295119	Human		name
597769825	CV3681664	single nucleotide variant	NM_023915.4(GPR87):c.265A>G (p.Ile89Val)	not specified [RCV004928176]	uncertain significance	3	151294981	151294981	Human		name
597769829	CV3681665	single nucleotide variant	NM_023915.4(GPR87):c.128T>C (p.Ile43Thr)	not specified [RCV004928177]	uncertain significance	3	151295118	151295118	Human		name
155953067	CV2264303	single nucleotide variant	NM_023915.4(GPR87):c.557A>C (p.Glu186Ala)	not specified [RCV004138223]	uncertain significance	3	151294689	151294689	Human		name
156057776	CV2316834	single nucleotide variant	NM_023915.4(GPR87):c.854A>T (p.Asp285Val)	not specified [RCV004172321]	uncertain significance	3	151294392	151294392	Human		name
156306562	CV2359989	single nucleotide variant	NM_023915.4(GPR87):c.533T>A (p.Ile178Asn)	not specified [RCV004212830]	uncertain significance	3	151294713	151294713	Human		name
155927878	CV2365999	single nucleotide variant	NM_023915.4(GPR87):c.772G>A (p.Val258Met)	not specified [RCV004207600]	uncertain significance	3	151294474	151294474	Human		name
156018154	CV2370235	single nucleotide variant	NM_023915.4(GPR87):c.850T>G (p.Leu284Val)	not specified [RCV004211109]	uncertain significance	3	151294396	151294396	Human		name
156206331	CV2385308	single nucleotide variant	NM_023915.4(GPR87):c.769G>A (p.Val257Ile)	not specified [RCV004230589]	uncertain significance	3	151294477	151294477	Human		name
156143716	CV2393601	single nucleotide variant	NM_023915.4(GPR87):c.721A>C (p.Ile241Leu)	not specified [RCV004231415]	uncertain significance	3	151294525	151294525	Human		name
156148746	CV2394517	single nucleotide variant	NM_023915.4(GPR87):c.680T>C (p.Ile227Thr)	not specified [RCV004240875]	uncertain significance	3	151294566	151294566	Human		name
401741176	CV2690415	single nucleotide variant	NM_023915.4(GPR87):c.410T>C (p.Ile137Thr)	not specified [RCV004302401]	uncertain significance	3	151294836	151294836	Human		name
401890681	CV2778289	single nucleotide variant	NM_023915.4(GPR87):c.456G>A (p.Met152Ile)	not specified [RCV004350344]	uncertain significance	3	151294790	151294790	Human		name
401923057	CV2825015	single nucleotide variant	NM_023915.4(GPR87):c.493G>A (p.Val165Ile)	not provided [RCV003434775]	likely benign	3	151294753	151294753	Human		name
405740219	CV3252140	single nucleotide variant	NM_023915.4(GPR87):c.533T>C (p.Ile178Thr)	not specified [RCV004391224]	uncertain significance	3	151294713	151294713	Human		name
405740229	CV3252141	single nucleotide variant	NM_023915.4(GPR87):c.586A>C (p.Lys196Gln)	not specified [RCV004391225]	uncertain significance	3	151294660	151294660	Human		name
405740246	CV3252143	single nucleotide variant	NM_023915.4(GPR87):c.871A>G (p.Ile291Val)	not specified [RCV004391227]	uncertain significance	3	151294375	151294375	Human		name
407479942	CV3436819	single nucleotide variant	NM_023915.4(GPR87):c.729G>C (p.Gln243His)	not specified [RCV004632564]	uncertain significance	3	151294517	151294517	Human		name
597769806	CV3681660	single nucleotide variant	NM_023915.4(GPR87):c.607T>C (p.Trp203Arg)	not specified [RCV004928172]	uncertain significance	3	151294639	151294639	Human		name
597769820	CV3681663	single nucleotide variant	NM_023915.4(GPR87):c.599G>A (p.Gly200Glu)	not specified [RCV004928175]	uncertain significance	3	151294647	151294647	Human		name
598234145	CV3967407	single nucleotide variant	NM_023915.4(GPR87):c.788C>A (p.Thr263Asn)	not specified [RCV005342864]	uncertain significance	3	151294458	151294458	Human		name
598274720	CV3967408	single nucleotide variant	NM_023915.4(GPR87):c.931C>T (p.Pro311Ser)	not specified [RCV005351550]	uncertain significance	3	151294315	151294315	Human		name
598274722	CV3967409	single nucleotide variant	NM_023915.4(GPR87):c.352T>G (p.Ser118Ala)	not specified [RCV005351551]	uncertain significance	3	151294894	151294894	Human		name
156274345	CV2254791	single nucleotide variant	NM_023915.4(GPR87):c.1060G>T (p.Asp354Tyr)	not specified [RCV004115258]	uncertain significance	3	151294186	151294186	Human		name
155919048	CV2254792	single nucleotide variant	NM_023915.4(GPR87):c.1067C>T (p.Thr356Ile)	not specified [RCV004115259]	uncertain significance	3	151294179	151294179	Human		name
156274365	CV2254793	single nucleotide variant	NM_023915.4(GPR87):c.1069G>T (p.Asp357Tyr)	not specified [RCV004115260]	uncertain significance	3	151294177	151294177	Human		name
156039366	CV2384259	single nucleotide variant	NM_023915.4(GPR87):c.1040C>G (p.Ser347Trp)	not specified [RCV004227648]	uncertain significance	3	151294206	151294206	Human		name

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