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Variants search result for Homo sapiens
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25 records found for search term Ggh
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401753942CV2716940single nucleotide variantNM_003878.3(GGH):c.17G>A (p.Cys6Tyr)not specified [RCV004330029]uncertain significance86303875263038752Humanname
402518854CV2936428insertionNM_003878.3(GGH):c.224+16_224+17insGnot provided [RCV003662994]likely benign86303563963035640Humanname
405734527CV3254604single nucleotide variantNM_003878.3(GGH):c.13G>A (p.Gly5Ser)not specified [RCV004390422]uncertain significance86303875663038756Humanname
15164273CV711599single nucleotide variantNM_003878.3(GGH):c.174G>A (p.Ala58=)not provided [RCV000970681]benign86303570663035706Humanname
156071865CV2201290single nucleotide variantNM_003878.3(GGH):c.77C>A (p.Pro26His)not specified [RCV004077424]uncertain significance86303869263038692Humanname
156020880CV2226595single nucleotide variantNM_003878.3(GGH):c.179A>G (p.Tyr60Cys)not specified [RCV004101845]uncertain significance86303570163035701Humanname
15097907CV723164single nucleotide variantNM_003878.3(GGH):c.268A>G (p.Ile90Val)not provided [RCV000891610]benign86303017463030174Humanname
156070787CV2204083single nucleotide variantNM_003878.3(GGH):c.704A>G (p.Lys235Arg)not specified [RCV004076548]uncertain significance86301762463017624Humanname
156239070CV2221228single nucleotide variantNM_003878.3(GGH):c.587A>G (p.Lys196Arg)not specified [RCV004094666]uncertain significance86302409963024099Humanname
155926229CV2258722single nucleotide variantNM_003878.3(GGH):c.688A>G (p.Thr230Ala)not specified [RCV004117961]uncertain significance86302391663023916Humanname
156250000CV2286666single nucleotide variantNM_003878.3(GGH):c.691A>G (p.Met231Val)not specified [RCV004142504]uncertain significance86302391363023913Humanname
156258761CV2304886single nucleotide variantNM_003878.3(GGH):c.700T>C (p.Tyr234His)not specified [RCV004168806]uncertain significance86301762863017628Humanname
156246522CV2310612single nucleotide variantNM_003878.3(GGH):c.535A>G (p.Thr179Ala)not specified [RCV004157275]likely benign86302415163024151Humanname
156084387CV2381981single nucleotide variantNM_003878.3(GGH):c.923T>C (p.Ile308Thr)not specified [RCV004225911]uncertain significance86301536663015366Humanname
329369894CV2424973single nucleotide variantNM_003878.3(GGH):c.467T>C (p.Val156Ala)not specified [RCV004250637]uncertain significance86302619063026190Humanname
329386726CV2428403single nucleotide variantNM_003878.3(GGH):c.304C>G (p.Leu102Val)not specified [RCV004253207]uncertain significance86302723763027237Humanname
401745082CV2698461single nucleotide variantNM_003878.3(GGH):c.481C>T (p.Pro161Ser)not specified [RCV004298971]uncertain significance86302617663026176Humanname
401779987CV2725809single nucleotide variantNM_003878.3(GGH):c.464C>T (p.Thr155Ile)not specified [RCV004316281]uncertain significance86302619363026193Humanname
405734533CV3254605single nucleotide variantNM_003878.3(GGH):c.779A>G (p.His260Arg)not specified [RCV004390423]uncertain significance86301754963017549Humanname
405734541CV3254606single nucleotide variantNM_003878.3(GGH):c.809A>C (p.Tyr270Ser)not specified [RCV004390424]uncertain significance86301751963017519Humanname
405734547CV3254607single nucleotide variantNM_003878.3(GGH):c.833A>G (p.Glu278Gly)not specified [RCV004390425]uncertain significance86301749563017495Humanname
405734558CV3254608single nucleotide variantNM_003878.3(GGH):c.883G>A (p.Ala295Thr)not specified [RCV004390426]uncertain significance86301540663015406Humanname
407513012CV3433085single nucleotide variantNM_003878.3(GGH):c.797A>C (p.Lys266Thr)not specified [RCV004626993]uncertain significance86301753163017531Humanname
597759079CV3684285single nucleotide variantNM_003878.3(GGH):c.634A>C (p.Lys212Gln)not specified [RCV004925427]uncertain significance86302397063023970Humanname
598251020CV3967155single nucleotide variantNM_003878.3(GGH):c.362G>T (p.Ser121Ile)not specified [RCV005345809]uncertain significance86302629563026295Humanname