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Variants search result for All species
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17 records found for search term Zdhhc3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15107073CV748278single nucleotide variantNM_001135179.2(ZDHHC3):c.306+504G>Anot provided [RCV000915880]likely benign34495862744958627Humanname
8644853CV104260single nucleotide variantNM_001135179.2(ZDHHC3):c.147C>T (p.Ile49=)not provided [RCV000084658]not provided34495929044959290Humanname
8644854CV104261single nucleotide variantNM_001135179.2(ZDHHC3):c.86A>G (p.Tyr29Cys)not provided [RCV000084659]|not specified [RCV004019584]uncertain significance|not provided34495935144959351Humanname
401741832CV2676536single nucleotide variantNM_001135179.2(ZDHHC3):c.83C>G (p.Pro28Arg)not specified [RCV004288727]uncertain significance34495935444959354Humanname
597724832CV3631083single nucleotide variantNM_001135179.2(ZDHHC3):c.83C>A (p.Pro28His)not specified [RCV004888204]uncertain significance34495935444959354Humanname
155924833CV2211660single nucleotide variantNM_001135179.2(ZDHHC3):c.136G>A (p.Ala46Thr)not specified [RCV004084552]uncertain significance34495930144959301Humanname
155933698CV2228975single nucleotide variantNM_001135179.2(ZDHHC3):c.241A>G (p.Ile81Val)not specified [RCV004098764]uncertain significance34495919644959196Humanname
155921016CV2340379single nucleotide variantNM_001135179.2(ZDHHC3):c.212G>A (p.Arg71Gln)not specified [RCV004197110]uncertain significance34495922544959225Humanname
329365456CV2444890single nucleotide variantNM_001135179.2(ZDHHC3):c.287G>A (p.Arg96Gln)not specified [RCV004259126]uncertain significance34495915044959150Humanname
405813036CV3349794single nucleotide variantNM_001135179.2(ZDHHC3):c.220G>A (p.Val74Met)not specified [RCV004483647]uncertain significance34495921744959217Humanname
8644852CV104259single nucleotide variantNM_001135179.2(ZDHHC3):c.617G>C (p.Ser206Thr)not provided [RCV000084657]not provided34492943044929430Humanname
155967689CV2265797single nucleotide variantNM_001135179.2(ZDHHC3):c.346G>A (p.Glu116Lys)not specified [RCV004126413]uncertain significance34494525344945253Humanname
405813038CV3349795single nucleotide variantNM_001135179.2(ZDHHC3):c.398G>A (p.Cys133Tyr)not specified [RCV004483648]uncertain significance34494520144945201Humanname
405813040CV3349796single nucleotide variantNM_001135179.2(ZDHHC3):c.682C>T (p.Leu228Phe)not specified [RCV004483649]uncertain significance34492936544929365Humanname
597793407CV3631082single nucleotide variantNM_001135179.2(ZDHHC3):c.343A>G (p.Ile115Val)not specified [RCV004877307]uncertain significance34494525644945256Humanname
598198259CV3927013single nucleotide variantNM_001135179.2(ZDHHC3):c.386G>A (p.Cys129Tyr)not specified [RCV005313762]uncertain significance34494521344945213Humanname
598198267CV3927014single nucleotide variantNM_001135179.2(ZDHHC3):c.670G>A (p.Gly224Ser)not specified [RCV005313763]uncertain significance34492937744929377Humanname