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20 records found for search term Cldn7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597782660CV3660338single nucleotide variantNM_001307.6(CLDN7):c.8A>G (p.Asn3Ser)not specified [RCV004900048]uncertain significance1772620367262036Humanname
597782664CV3660339single nucleotide variantNM_001307.6(CLDN7):c.262C>T (p.Leu88=)not specified [RCV004900049]likely benign1772609477260947Humanname
15156068CV727396single nucleotide variantNM_001307.6(CLDN7):c.297G>A (p.Thr99=)not provided [RCV000880547]likely benign1772609127260912Humanname
156190188CV2325453single nucleotide variantNM_001307.6(CLDN7):c.83C>T (p.Pro28Leu)not specified [RCV004179908]uncertain significance1772619617261961Humanname
401757900CV2731528single nucleotide variantNM_001307.6(CLDN7):c.495C>T (p.Ile165=)not specified [RCV004330877]likely benign1772605157260515Humanname
597782657CV3660337single nucleotide variantNM_001307.6(CLDN7):c.295A>G (p.Thr99Ala)not specified [RCV004900047]uncertain significance1772609147260914Humanname
597782668CV3660340single nucleotide variantNM_001307.6(CLDN7):c.268C>G (p.Leu90Val)not specified [RCV004900050]uncertain significance1772609417260941Humanname
598243026CV3944544single nucleotide variantNM_001307.6(CLDN7):c.256G>T (p.Val86Phe)not specified [RCV005321841]uncertain significance1772609537260953Humanname
156400494CV2199216single nucleotide variantNM_001307.6(CLDN7):c.595C>T (p.Arg199Cys)not specified [RCV004080600]uncertain significance1772604157260415Humanname
156118818CV2228757single nucleotide variantNM_001307.6(CLDN7):c.326G>C (p.Gly109Ala)not specified [RCV004093227]uncertain significance1772608837260883Humanname
156365200CV2272074single nucleotide variantNM_001307.6(CLDN7):c.299T>C (p.Met100Thr)not specified [RCV004124869]uncertain significance1772609107260910Humanname
155902747CV2274754single nucleotide variantNM_001307.6(CLDN7):c.317G>T (p.Arg106Leu)not specified [RCV004139111]uncertain significance1772608927260892Humanname
401783465CV2723599single nucleotide variantNM_001307.6(CLDN7):c.523G>C (p.Val175Leu)not specified [RCV004323991]uncertain significance1772604877260487Humanname
401879086CV2778143single nucleotide variantNM_001307.6(CLDN7):c.551G>A (p.Cys184Tyr)not specified [RCV004348081]uncertain significance1772604597260459Humanname
405685786CV3306645single nucleotide variantNM_001307.6(CLDN7):c.391C>G (p.Leu131Val)not specified [RCV004444363]uncertain significance1772607247260724Humanname
405685791CV3306646single nucleotide variantNM_001307.6(CLDN7):c.391C>T (p.Leu131Phe)not specified [RCV004444364]uncertain significance1772607247260724Humanname
405685798CV3306647single nucleotide variantNM_001307.6(CLDN7):c.508G>A (p.Ala170Thr)not specified [RCV004444365]uncertain significance1772605027260502Humanname
598243020CV3944543single nucleotide variantNM_001307.6(CLDN7):c.451C>T (p.Pro151Ser)not specified [RCV005321840]uncertain significance1772606647260664Humanname
598243035CV3944545single nucleotide variantNM_001307.6(CLDN7):c.550T>G (p.Cys184Gly)not specified [RCV005321842]uncertain significance1772604607260460Humanname
598243041CV3944546single nucleotide variantNM_001307.6(CLDN7):c.559C>T (p.Pro187Ser)not specified [RCV005321843]uncertain significance1772604517260451Humanname