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Variants search result for Homo sapiens
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31 records found for search term Gpr139
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597744572CV3684745single nucleotide variantNM_001002911.4(GPR139):c.8A>T (p.His3Leu)not specified [RCV004922285]uncertain significance162007360920073609Humanname
156044156CV2397082single nucleotide variantNM_001002911.4(GPR139):c.85C>T (p.Pro29Ser)not specified [RCV004236592]uncertain significance162007353220073532Humanname
407526132CV3440071single nucleotide variantNM_001002911.4(GPR139):c.41T>G (p.Leu14Arg)not specified [RCV004632339]uncertain significance162007357620073576Humanname
597790042CV3684748single nucleotide variantNM_001002911.4(GPR139):c.97T>C (p.Tyr33His)not specified [RCV004933022]uncertain significance162007352020073520Humanname
8635692CV90915single nucleotide variantNM_001002911.2(GPR139):c.654C>T (p.Leu218=)Malignant melanoma [RCV000071013]not provided162003214320032143Humanname
156172027CV2312616single nucleotide variantNM_001002911.4(GPR139):c.235T>C (p.Phe79Leu)not specified [RCV004169354]uncertain significance162003256220032562Humanname
156394859CV2328233single nucleotide variantNM_001002911.4(GPR139):c.242T>G (p.Val81Gly)not specified [RCV004173322]uncertain significance162003255520032555Humanname
329368634CV2450388single nucleotide variantNM_001002911.4(GPR139):c.101G>T (p.Ser34Ile)not specified [RCV004265323]uncertain significance162007351620073516Humanname
597744567CV3684744single nucleotide variantNM_001002911.4(GPR139):c.267T>A (p.Asp89Glu)not specified [RCV004922284]uncertain significance162003253020032530Humanname
597790050CV3684746single nucleotide variantNM_001002911.4(GPR139):c.244T>C (p.Phe82Leu)not specified [RCV004933020]uncertain significance162003255320032553Humanname
155966908CV2280189single nucleotide variantNM_001002911.4(GPR139):c.424C>A (p.Pro142Thr)not specified [RCV004140413]uncertain significance162003237320032373Humanname
156180644CV2324486single nucleotide variantNM_001002911.4(GPR139):c.467G>T (p.Cys156Phe)not specified [RCV004178968]uncertain significance162003233020032330Humanname
156358693CV2328053single nucleotide variantNM_001002911.4(GPR139):c.613A>G (p.Ile205Val)not specified [RCV004173179]uncertain significance162003218420032184Humanname
156105198CV2361150single nucleotide variantNM_001002911.4(GPR139):c.413C>T (p.Thr138Met)not specified [RCV004216338]uncertain significance162003238420032384Humanname
156269866CV2379424single nucleotide variantNM_001002911.4(GPR139):c.691T>C (p.Phe231Leu)not specified [RCV004223875]uncertain significance162003210620032106Humanname
156225035CV2390464single nucleotide variantNM_001002911.4(GPR139):c.446T>C (p.Ile149Thr)not specified [RCV004239006]uncertain significance162003235120032351Humanname
401760804CV2706100single nucleotide variantNM_001002911.4(GPR139):c.362C>T (p.Pro121Leu)not specified [RCV004314790]uncertain significance162003243520032435Humanname
405716738CV3255141single nucleotide variantNM_001002911.4(GPR139):c.520T>A (p.Tyr174Asn)not specified [RCV004388289]uncertain significance162003227720032277Humanname
405716744CV3255142single nucleotide variantNM_001002911.4(GPR139):c.674A>G (p.Lys225Arg)not specified [RCV004388290]uncertain significance162003212320032123Humanname
405716752CV3255143single nucleotide variantNM_001002911.4(GPR139):c.676A>T (p.Thr226Ser)not specified [RCV004388291]uncertain significance162003212120032121Humanname
405716759CV3255144single nucleotide variantNM_001002911.4(GPR139):c.772C>A (p.Gln258Lys)not specified [RCV004388292]uncertain significance162003202520032025Humanname
405716768CV3255145single nucleotide variantNM_001002911.4(GPR139):c.798G>A (p.Met266Ile)not specified [RCV004388293]uncertain significance162003199920031999Humanname
405716773CV3255146single nucleotide variantNM_001002911.4(GPR139):c.989C>T (p.Ala330Val)not specified [RCV004388294]uncertain significance162003180820031808Humanname
407526121CV3440067single nucleotide variantNM_001002911.4(GPR139):c.301G>A (p.Asp101Asn)not specified [RCV004632335]likely benign162003249620032496Humanname
407526128CV3440069single nucleotide variantNM_001002911.4(GPR139):c.580G>A (p.Val194Met)not specified [RCV004632337]uncertain significance162003221720032217Humanname
597790047CV3684747single nucleotide variantNM_001002911.4(GPR139):c.635G>T (p.Arg212Met)not specified [RCV004933021]uncertain significance162003216220032162Humanname
598274171CV3971011single nucleotide variantNM_001002911.4(GPR139):c.371T>C (p.Ile124Thr)not specified [RCV005351288]uncertain significance162003242620032426Humanname
598274173CV3971012single nucleotide variantNM_001002911.4(GPR139):c.965C>G (p.Thr322Arg)not specified [RCV005351289]uncertain significance162003183220031832Humanname
598274175CV3971013single nucleotide variantNM_001002911.4(GPR139):c.872G>A (p.Arg291Gln)not specified [RCV005351290]uncertain significance162003192520031925Humanname
598274177CV3971014single nucleotide variantNM_001002911.4(GPR139):c.965C>T (p.Thr322Ile)not specified [RCV005351291]uncertain significance162003183220031832Humanname
407526123CV3440068single nucleotide variantNM_001002911.4(GPR139):c.1048A>G (p.Lys350Glu)not specified [RCV004632336]uncertain significance162003174920031749Humanname