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Variants search result for Homo sapiens
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21 records found for search term Tppp2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405774841CV3343889single nucleotide variantNM_173846.5(TPPP2):c.32G>A (p.Arg11Gln)not specified [RCV004470925]uncertain significance142103061321030613Humanname
156031319CV2202658single nucleotide variantNM_173846.5(TPPP2):c.251G>A (p.Gly84Glu)not specified [RCV004082909]uncertain significance142103108921031089Humanname
156296002CV2233790single nucleotide variantNM_173846.5(TPPP2):c.218C>T (p.Ala73Val)not specified [RCV004100224]uncertain significance142103105621031056Humanname
156362487CV2330214single nucleotide variantNM_173846.5(TPPP2):c.148G>A (p.Val50Met)not specified [RCV004187673]uncertain significance142103072921030729Humanname
329349448CV2434623single nucleotide variantNM_173846.5(TPPP2):c.157G>A (p.Val53Met)not specified [RCV004248348]uncertain significance142103073821030738Humanname
329350525CV2471694single nucleotide variantNM_173846.5(TPPP2):c.184G>A (p.Ala62Thr)not specified [RCV004286977]uncertain significance142103102221031022Humanname
401745061CV2714150single nucleotide variantNM_173846.5(TPPP2):c.188G>A (p.Arg63Gln)not specified [RCV004317401]uncertain significance142103102621031026Humanname
405774818CV3343885single nucleotide variantNM_173846.5(TPPP2):c.197C>T (p.Thr66Met)not specified [RCV004470921]uncertain significance142103103521031035Humanname
405774824CV3343886single nucleotide variantNM_173846.5(TPPP2):c.227A>T (p.Glu76Val)not specified [RCV004470922]uncertain significance142103106521031065Humanname
598201093CV3928370single nucleotide variantNM_173846.5(TPPP2):c.292A>G (p.Met98Val)not specified [RCV005290106]uncertain significance142103113021031130Humanname
156144534CV2200169single nucleotide variantNM_173846.5(TPPP2):c.476A>G (p.Tyr159Cys)not specified [RCV004069736]uncertain significance142103204021032040Humanname
156071716CV2353222single nucleotide variantNM_173846.5(TPPP2):c.436C>T (p.Arg146Trp)not specified [RCV004203690]uncertain significance142103200021032000Humanname
329349716CV2434481single nucleotide variantNM_173846.5(TPPP2):c.437G>A (p.Arg146Gln)not specified [RCV004254190]uncertain significance142103200121032001Humanname
329349976CV2457271single nucleotide variantNM_173846.5(TPPP2):c.395A>C (p.Glu132Ala)not specified [RCV004267123]uncertain significance142103195921031959Humanname
405774831CV3343887single nucleotide variantNM_173846.5(TPPP2):c.305A>G (p.Asp102Gly)not specified [RCV004470923]uncertain significance142103114321031143Humanname
405774835CV3343888single nucleotide variantNM_173846.5(TPPP2):c.306C>G (p.Asp102Glu)not specified [RCV004470924]uncertain significance142103114421031144Humanname
405774847CV3343890single nucleotide variantNM_173846.5(TPPP2):c.406G>C (p.Glu136Gln)not specified [RCV004470926]uncertain significance142103197021031970Humanname
597689780CV3611334single nucleotide variantNM_173846.5(TPPP2):c.397C>T (p.Arg133Cys)not specified [RCV004878207]uncertain significance142103196121031961Humanname
598265071CV3928368single nucleotide variantNM_173846.5(TPPP2):c.392A>G (p.Lys131Arg)not specified [RCV005281022]uncertain significance142103195621031956Humanname
598201088CV3928369single nucleotide variantNM_173846.5(TPPP2):c.491C>T (p.Thr164Ile)not specified [RCV005290105]uncertain significance142103205521032055Humanname
15199967CV702800single nucleotide variantNM_173846.5(TPPP2):c.495C>G (p.Tyr165Ter)not provided [RCV000957194]benign142103205921032059Humanname