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Variants search result for Homo sapiens
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36 records found for search term Gprin2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597770043CV3681769single nucleotide variantNM_001385282.1(GPRIN2):c.19G>A (p.Glu7Lys)not specified [RCV004928223]uncertain significance104655071846550718Humanname
405755787CV3252278single nucleotide variantNM_001385282.1(GPRIN2):c.97C>T (p.Arg33Trp)not specified [RCV004393434]uncertain significance104655064046550640Humanname
597745822CV3681768single nucleotide variantNM_001385282.1(GPRIN2):c.34G>T (p.Ala12Ser)not specified [RCV004922560]uncertain significance104655070346550703Humanname
598186850CV3967485single nucleotide variantNM_001385282.1(GPRIN2):c.80G>A (p.Ser27Asn)not specified [RCV005353592]uncertain significance104655065746550657Humanname
405755768CV3252275single nucleotide variantNM_001385282.1(GPRIN2):c.185C>T (p.Pro62Leu)not specified [RCV004393431]uncertain significance104655055246550552Humanname
597745812CV3681766single nucleotide variantNM_001385282.1(GPRIN2):c.200A>G (p.Asn67Ser)not specified [RCV004922558]uncertain significance104655053746550537Humanname
597745817CV3681767single nucleotide variantNM_001385282.1(GPRIN2):c.212G>A (p.Ser71Asn)not specified [RCV004922559]uncertain significance104655052546550525Humanname
598234230CV3967486single nucleotide variantNM_001385282.1(GPRIN2):c.202C>A (p.Pro68Thr)not specified [RCV005342877]uncertain significance104655053546550535Humanname
155964116CV2282806single nucleotide variantNM_001385282.1(GPRIN2):c.305G>A (p.Gly102Asp)not specified [RCV004141654]uncertain significance104655043246550432Humanname
156383759CV2361667single nucleotide variantNM_001385282.1(GPRIN2):c.881C>T (p.Ala294Val)not specified [RCV004223155]uncertain significance104654985646549856Humanname
329401692CV2461111single nucleotide variantNM_001385282.1(GPRIN2):c.653C>T (p.Ala218Val)not specified [RCV004265253]uncertain significance104655008446550084Humanname
329382962CV2465422single nucleotide variantNM_001385282.1(GPRIN2):c.388A>T (p.Met130Leu)not specified [RCV004281196]uncertain significance104655034946550349Humanname
401735676CV2702843single nucleotide variantNM_001385282.1(GPRIN2):c.700C>A (p.Leu234Ile)not specified [RCV004321190]uncertain significance104655003746550037Humanname
401768405CV2716560single nucleotide variantNM_001385282.1(GPRIN2):c.655G>A (p.Glu219Lys)not specified [RCV004327636]uncertain significance104655008246550082Humanname
401879876CV2769793single nucleotide variantNM_001385282.1(GPRIN2):c.922T>C (p.Ser308Pro)not specified [RCV004353660]uncertain significance104654981546549815Humanname
405755775CV3252276single nucleotide variantNM_001385282.1(GPRIN2):c.571G>A (p.Ala191Thr)not specified [RCV004393432]uncertain significance104655016646550166Humanname
405755780CV3252277single nucleotide variantNM_001385282.1(GPRIN2):c.929C>A (p.Thr310Asn)not specified [RCV004393433]uncertain significance104654980846549808Humanname
407526903CV3436877single nucleotide variantNM_001385282.1(GPRIN2):c.688C>T (p.Pro230Ser)not specified [RCV004632614]likely benign104655004946550049Humanname
407526906CV3436878single nucleotide variantNM_001385282.1(GPRIN2):c.331G>C (p.Ala111Pro)not specified [RCV004632615]uncertain significance104655040646550406Humanname
407526912CV3436880single nucleotide variantNM_001385282.1(GPRIN2):c.505C>A (p.Pro169Thr)not specified [RCV004632617]uncertain significance104655023246550232Humanname
597770049CV3681770single nucleotide variantNM_001385282.1(GPRIN2):c.707G>A (p.Cys236Tyr)not specified [RCV004928224]uncertain significance104655003046550030Humanname
598186864CV3967488single nucleotide variantNM_001385282.1(GPRIN2):c.782T>C (p.Leu261Pro)not specified [RCV005353594]uncertain significance104654995546549955Humanname
598234237CV3967489single nucleotide variantNM_001385282.1(GPRIN2):c.710G>C (p.Gly237Ala)not specified [RCV005342878]uncertain significance104655002746550027Humanname
598234243CV3967490single nucleotide variantNM_001385282.1(GPRIN2):c.412A>G (p.Lys138Glu)not specified [RCV005342879]uncertain significance104655032546550325Humanname
156134247CV2196014single nucleotide variantNM_001385282.1(GPRIN2):c.1312C>T (p.Arg438Trp)not specified [RCV004072257]uncertain significance104654942546549425Humanname
156260465CV2204817single nucleotide variantNM_001385282.1(GPRIN2):c.1202A>G (p.Glu401Gly)not specified [RCV004075071]uncertain significance104654953546549535Humanname
156204486CV2331676single nucleotide variantNM_001385282.1(GPRIN2):c.1259G>A (p.Arg420Gln)not specified [RCV004184306]uncertain significance104654947846549478Humanname
155922707CV2347366single nucleotide variantNM_001385282.1(GPRIN2):c.1055C>T (p.Pro352Leu)not specified [RCV004207207]uncertain significance104654968246549682Humanname
155931316CV2362532single nucleotide variantNM_001385282.1(GPRIN2):c.1313G>A (p.Arg438Gln)not specified [RCV004213150]uncertain significance104654942446549424Humanname
329398420CV2464560single nucleotide variantNM_001385282.1(GPRIN2):c.1055C>A (p.Pro352Gln)not specified [RCV004278254]uncertain significance104654968246549682Humanname
401720759CV2673477single nucleotide variantNM_001385282.1(GPRIN2):c.1016C>T (p.Ala339Val)not specified [RCV004288446]likely benign104654972146549721Humanname
401734184CV2694463single nucleotide variantNM_001385282.1(GPRIN2):c.1135G>A (p.Val379Met)not specified [RCV004304626]uncertain significance104654960246549602Humanname
407526899CV3436875single nucleotide variantNM_001385282.1(GPRIN2):c.1297C>T (p.Arg433Trp)not specified [RCV004632613]uncertain significance104654944046549440Humanname
407504562CV3436876single nucleotide variantNM_001385282.1(GPRIN2):c.1325A>G (p.Gln442Arg)not specified [RCV004624009]uncertain significance104654941246549412Humanname
407526909CV3436879single nucleotide variantNM_001385282.1(GPRIN2):c.1051A>G (p.Ser351Gly)not specified [RCV004632616]uncertain significance104654968646549686Humanname
597745827CV3681771single nucleotide variantNM_001385282.1(GPRIN2):c.1027G>T (p.Ala343Ser)not specified [RCV004922561]uncertain significance104654971046549710Humanname