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Variants search result for Homo sapiens
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27 records found for search term Gzma
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156184444CV2377724single nucleotide variantNM_006144.4(GZMA):c.71A>T (p.Asp24Val)not specified [RCV004230313]uncertain significance55510547455105474Humanname
401873062CV2776420single nucleotide variantNM_006144.4(GZMA):c.46G>T (p.Val16Phe)not specified [RCV004355542]uncertain significance55510272855102728Humanname
597780504CV3685206single nucleotide variantNM_006144.4(GZMA):c.46G>A (p.Val16Ile)not specified [RCV004930678]likely benign55510272855102728Humanname
156363869CV2330098single nucleotide variantNM_006144.4(GZMA):c.190G>A (p.Val64Met)not specified [RCV004185588]uncertain significance55510559355105593Humanname
407504526CV3443709single nucleotide variantNM_006144.4(GZMA):c.116C>T (p.Ser39Leu)not specified [RCV004624096]uncertain significance55510551955105519Humanname
8631660CV86864single nucleotide variantNM_006144.3(GZMA):c.262G>A (p.Glu88Lys)Malignant melanoma [RCV000066955]not provided55510784055107840Humanname
155960145CV2204102single nucleotide variantNM_006144.4(GZMA):c.533T>C (p.Val178Ala)not specified [RCV004076915]uncertain significance55510830055108300Humanname
156243813CV2283303single nucleotide variantNM_006144.4(GZMA):c.641G>A (p.Ser214Asn)not specified [RCV004145965]uncertain significance55511003455110034Humanname
156003420CV2293463single nucleotide variantNM_006144.4(GZMA):c.518T>C (p.Ile173Thr)not specified [RCV004152706]uncertain significance55510828555108285Humanname
155988611CV2364006single nucleotide variantNM_006144.4(GZMA):c.545G>A (p.Arg182Gln)not specified [RCV004221017]uncertain significance55510831255108312Humanname
156171492CV2400688single nucleotide variantNM_006144.4(GZMA):c.779G>T (p.Gly260Val)not specified [RCV004242364]uncertain significance55511017255110172Humanname
401781081CV2734155single nucleotide variantNM_006144.4(GZMA):c.578T>C (p.Met193Thr)not specified [RCV004330663]uncertain significance55510834555108345Humanname
405720826CV3255819single nucleotide variantNM_006144.4(GZMA):c.725T>C (p.Val242Ala)not specified [RCV004388776]uncertain significance55511011855110118Humanname
407513581CV3443708single nucleotide variantNM_006144.4(GZMA):c.784G>A (p.Val262Ile)not specified [RCV004627203]uncertain significance55511017755110177Humanname
407513578CV3443710single nucleotide variantNM_006144.4(GZMA):c.755A>G (p.Asn252Ser)not specified [RCV004627204]likely benign55511014855110148Humanname
407513574CV3443711single nucleotide variantNM_006144.4(GZMA):c.375A>C (p.Lys125Asn)not specified [RCV004627205]uncertain significance55510814255108142Humanname
407513570CV3443712single nucleotide variantNM_006144.4(GZMA):c.338G>A (p.Gly113Asp)not specified [RCV004627206]uncertain significance55510791655107916Humanname
407513563CV3443714single nucleotide variantNM_006144.4(GZMA):c.477T>G (p.Ser159Arg)not specified [RCV004627208]uncertain significance55510824455108244Humanname
407513559CV3443715single nucleotide variantNM_006144.4(GZMA):c.605G>A (p.Arg202Gln)not specified [RCV004627209]uncertain significance55510837255108372Humanname
597757562CV3685203single nucleotide variantNM_006144.4(GZMA):c.413A>T (p.Lys138Met)not specified [RCV004925104]uncertain significance55510818055108180Humanname
597757566CV3685204single nucleotide variantNM_006144.4(GZMA):c.616G>C (p.Asp206His)not specified [RCV004925105]uncertain significance55510838355108383Humanname
597780502CV3685205single nucleotide variantNM_006144.4(GZMA):c.452C>T (p.Ala151Val)not specified [RCV004930677]uncertain significance55510821955108219Humanname
598253810CV3975011single nucleotide variantNM_006144.4(GZMA):c.713G>A (p.Arg238His)not specified [RCV005346327]likely benign55511010655110106Humanname
598253818CV3975012single nucleotide variantNM_006144.4(GZMA):c.418G>C (p.Asp140His)not specified [RCV005346328]uncertain significance55510818555108185Humanname
15151023CV709945single nucleotide variantNM_006144.4(GZMA):c.583A>G (p.Met195Val)not provided [RCV000968054]benign55510835055108350Humanname
8626035CV81179single nucleotide variantNM_006144.3(GZMA):c.655G>A (p.Glu219Lys)Malignant melanoma [RCV000061257]not provided55511004855110048Humanname
8631661CV86865single nucleotide variantNM_006144.3(GZMA):c.680C>T (p.Ser227Phe)Malignant melanoma [RCV000066956]not provided55511007355110073Humanname