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Variants search result for Homo sapiens
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29 records found for search term Gpr171
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15156152CV720251single nucleotide variantNM_013308.4(GPR171):c.15G>A (p.Ser5=)not provided [RCV000880566]benign3151199372151199372Humanname
8630644CV85799single nucleotide variantNM_013308.3(GPR171):c.177C>T (p.Ala59=)Malignant melanoma [RCV000065882]not provided3151199210151199210Humanname
401896636CV2791839single nucleotide variantNM_013308.4(GPR171):c.28G>A (p.Val10Ile)not specified [RCV004359286]uncertain significance3151199359151199359Humanname
401923059CV2825013single nucleotide variantNM_013308.4(GPR171):c.879C>T (p.Arg293=)not provided [RCV003434774]likely benign3151198508151198508Humanname
401944692CV2840484single nucleotide variantNM_013308.4(GPR171):c.735G>A (p.Pro245=)not provided [RCV003457398]likely benign3151198652151198652Humanname
407479860CV3436674single nucleotide variantNM_013308.4(GPR171):c.43G>A (p.Glu15Lys)not specified [RCV004632436]uncertain significance3151199344151199344Humanname
155999857CV2287319single nucleotide variantNM_013308.4(GPR171):c.168G>C (p.Leu56Phe)not specified [RCV004146944]uncertain significance3151199219151199219Humanname
405738312CV3255317single nucleotide variantNM_013308.4(GPR171):c.122A>G (p.Gln41Arg)not specified [RCV004390944]uncertain significance3151199265151199265Humanname
407479855CV3436673single nucleotide variantNM_013308.4(GPR171):c.229G>A (p.Val77Met)not specified [RCV004632435]uncertain significance3151199158151199158Humanname
597744925CV3684898single nucleotide variantNM_013308.4(GPR171):c.113C>T (p.Ala38Val)not specified [RCV004922362]uncertain significance3151199274151199274Humanname
8630645CV85800single nucleotide variantNM_013308.3(GPR171):c.176C>T (p.Ala59Val)Malignant melanoma [RCV000065883]not provided3151199211151199211Humanname
156399579CV2205203single nucleotide variantNM_013308.4(GPR171):c.722T>C (p.Ile241Thr)not specified [RCV004079837]uncertain significance3151198665151198665Humanname
156238342CV2265401single nucleotide variantNM_013308.4(GPR171):c.552T>G (p.Cys184Trp)not specified [RCV004128278]uncertain significance3151198835151198835Humanname
155998456CV2287153single nucleotide variantNM_013308.4(GPR171):c.593C>G (p.Ser198Cys)not specified [RCV004146806]uncertain significance3151198794151198794Humanname
156068262CV2317976single nucleotide variantNM_013308.4(GPR171):c.821C>T (p.Ala274Val)not specified [RCV004177095]uncertain significance3151198566151198566Humanname
156009797CV2362040single nucleotide variantNM_013308.4(GPR171):c.775A>G (p.Thr259Ala)not specified [RCV004209852]uncertain significance3151198612151198612Humanname
329358024CV2453863single nucleotide variantNM_013308.4(GPR171):c.436A>T (p.Met146Leu)not specified [RCV004271259]uncertain significance3151198951151198951Humanname
329397685CV2463910single nucleotide variantNM_013308.4(GPR171):c.764C>G (p.Thr255Ser)not specified [RCV004279979]likely benign3151198623151198623Humanname
401892878CV2758179single nucleotide variantNM_013308.4(GPR171):c.545T>A (p.Phe182Tyr)not specified [RCV004341549]uncertain significance3151198842151198842Humanname
401888327CV2788334single nucleotide variantNM_013308.4(GPR171):c.841G>T (p.Asp281Tyr)not specified [RCV004352913]uncertain significance3151198546151198546Humanname
401926551CV2825014single nucleotide variantNM_013308.4(GPR171):c.520A>G (p.Arg174Gly)not provided [RCV003437969]uncertain significance3151198867151198867Humanname
405738328CV3255319single nucleotide variantNM_013308.4(GPR171):c.860A>G (p.His287Arg)not specified [RCV004390946]uncertain significance3151198527151198527Humanname
597744929CV3684899single nucleotide variantNM_013308.4(GPR171):c.796G>T (p.Ala266Ser)not specified [RCV004922363]uncertain significance3151198591151198591Humanname
597744934CV3684900single nucleotide variantNM_013308.4(GPR171):c.596A>G (p.Asn199Ser)not specified [RCV004922364]uncertain significance3151198791151198791Humanname
597744939CV3684901single nucleotide variantNM_013308.4(GPR171):c.899T>C (p.Phe300Ser)not specified [RCV004922365]uncertain significance3151198488151198488Humanname
597789866CV3684902single nucleotide variantNM_013308.4(GPR171):c.578C>T (p.Ala193Val)not specified [RCV004933094]uncertain significance3151198809151198809Humanname
598274400CV3971156single nucleotide variantNM_013308.4(GPR171):c.956C>T (p.Ala319Val)not specified [RCV005351403]uncertain significance3151198431151198431Humanname
598274403CV3971157single nucleotide variantNM_013308.4(GPR171):c.689C>T (p.Thr230Met)not specified [RCV005351404]uncertain significance3151198698151198698Humanname
598274405CV3971158single nucleotide variantNM_013308.4(GPR171):c.410T>C (p.Val137Ala)not specified [RCV005351405]uncertain significance3151198977151198977Humanname