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Variants search result for Homo sapiens
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39 records found for search term Atg4c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407503958CV3484805single nucleotide variantNM_032852.4(ATG4C):c.98C>G (p.Thr33Arg)not specified [RCV004670392]uncertain significance16280519362805193Humanname
597701361CV3602806single nucleotide variantNM_032852.4(ATG4C):c.73T>G (p.Tyr25Asp)not specified [RCV004859975]uncertain significance16280385962803859Humanname
156232554CV2199750single nucleotide variantNM_032852.4(ATG4C):c.130C>A (p.Leu44Ile)not specified [RCV004072475]uncertain significance16280522562805225Humanname
155902061CV2274619single nucleotide variantNM_032852.4(ATG4C):c.238C>T (p.Arg80Cys)not specified [RCV004139008]uncertain significance16281665262816652Humanname
156169393CV2315455single nucleotide variantNM_032852.4(ATG4C):c.199A>G (p.Ile67Val)not specified [RCV004167408]uncertain significance16281661362816613Humanname
401774146CV2691533single nucleotide variantNM_032852.4(ATG4C):c.146A>C (p.His49Pro)not specified [RCV004305369]uncertain significance16280524162805241Humanname
405700840CV3279896single nucleotide variantNM_032852.4(ATG4C):c.178C>T (p.Pro60Ser)not specified [RCV004425378]uncertain significance16281659262816592Humanname
405700847CV3279897single nucleotide variantNM_032852.4(ATG4C):c.275G>A (p.Arg92Lys)not specified [RCV004425379]uncertain significance16281668962816689Humanname
597755951CV3602843single nucleotide variantNM_032852.4(ATG4C):c.294A>G (p.Ile98Met)not specified [RCV004868161]uncertain significance16281670862816708Humanname
155935541CV2225627single nucleotide variantNM_032852.4(ATG4C):c.596A>G (p.Lys199Arg)not specified [RCV004100998]uncertain significance16281920662819206Humanname
155944795CV2269332single nucleotide variantNM_032852.4(ATG4C):c.617A>T (p.Asp206Val)not specified [RCV004130733]uncertain significance16281922762819227Humanname
156099688CV2294655single nucleotide variantNM_032852.4(ATG4C):c.856G>A (p.Asp286Asn)not specified [RCV004161907]uncertain significance16282909962829099Humanname
156193867CV2297031single nucleotide variantNM_032852.4(ATG4C):c.935G>T (p.Gly312Val)not specified [RCV004150954]uncertain significance16283403962834039Humanname
156072234CV2335011single nucleotide variantNM_032852.4(ATG4C):c.653T>C (p.Ile218Thr)not specified [RCV004182102]uncertain significance16281926362819263Humanname
156223266CV2355567single nucleotide variantNM_032852.4(ATG4C):c.657A>C (p.Glu219Asp)not specified [RCV004205412]uncertain significance16281926762819267Humanname
156147076CV2357982single nucleotide variantNM_032852.4(ATG4C):c.389G>A (p.Gly130Asp)not specified [RCV004209762]uncertain significance16281680362816803Humanname
156074910CV2377009single nucleotide variantNM_032852.4(ATG4C):c.620C>T (p.Ser207Phe)not specified [RCV004229690]uncertain significance16281923062819230Humanname
156135752CV2379963single nucleotide variantNM_032852.4(ATG4C):c.411T>G (p.Asp137Glu)not specified [RCV004222107]uncertain significance16281902162819021Humanname
156146894CV2397454single nucleotide variantNM_032852.4(ATG4C):c.590A>T (p.His197Leu)not specified [RCV004238964]uncertain significance16281920062819200Humanname
405700853CV3279898single nucleotide variantNM_032852.4(ATG4C):c.351G>T (p.Gln117His)not specified [RCV004425380]uncertain significance16281676562816765Humanname
405700860CV3279899single nucleotide variantNM_032852.4(ATG4C):c.718A>G (p.Ile240Val)not specified [RCV004425381]uncertain significance16281932862819328Humanname
405700866CV3279900single nucleotide variantNM_032852.4(ATG4C):c.980C>G (p.Pro327Arg)not specified [RCV004425382]uncertain significance16283408462834084Humanname
407503979CV3484816single nucleotide variantNM_032852.4(ATG4C):c.578A>G (p.Asn193Ser)not specified [RCV004670398]uncertain significance16281918862819188Humanname
597756003CV3602815single nucleotide variantNM_032852.4(ATG4C):c.917A>G (p.Tyr306Cys)not specified [RCV004868149]uncertain significance16282916062829160Humanname
597755999CV3602818single nucleotide variantNM_032852.4(ATG4C):c.346G>A (p.Gly116Ser)not specified [RCV004868150]uncertain significance16281676062816760Humanname
597755995CV3602826single nucleotide variantNM_032852.4(ATG4C):c.676A>G (p.Lys226Glu)not specified [RCV004868151]uncertain significance16281928662819286Humanname
597701477CV3602854single nucleotide variantNM_032852.4(ATG4C):c.803A>T (p.Asn268Ile)not specified [RCV004859989]uncertain significance16282904662829046Humanname
598169278CV3918304single nucleotide variantNM_032852.4(ATG4C):c.523A>C (p.Thr175Pro)not specified [RCV005284239]uncertain significance16281913362819133Humanname
598169310CV3918311single nucleotide variantNM_032852.4(ATG4C):c.844G>A (p.Asp282Asn)not specified [RCV005284246]uncertain significance16282908762829087Humanname
598169366CV3918327single nucleotide variantNM_032852.4(ATG4C):c.802A>G (p.Asn268Asp)not specified [RCV005284259]uncertain significance16282904562829045Humanname
598169413CV3918338single nucleotide variantNM_032852.4(ATG4C):c.446G>C (p.Trp149Ser)not specified [RCV005284269]uncertain significance16281905662819056Humanname
155972197CV2228100single nucleotide variantNM_032852.4(ATG4C):c.1301A>G (p.Asn434Ser)not specified [RCV004096326]uncertain significance16286408362864083Humanname
156074435CV2331660single nucleotide variantNM_032852.4(ATG4C):c.1127G>A (p.Arg376Gln)not specified [RCV004184290]uncertain significance16284146562841465Humanname
405689448CV3279893single nucleotide variantNM_032852.4(ATG4C):c.1037C>T (p.Pro346Leu)not specified [RCV004423392]uncertain significance16283480062834800Humanname
405689451CV3279894single nucleotide variantNM_032852.4(ATG4C):c.1145G>C (p.Cys382Ser)not specified [RCV004423393]uncertain significance16284148362841483Humanname
405689458CV3279895single nucleotide variantNM_032852.4(ATG4C):c.1153G>A (p.Gly385Arg)not specified [RCV004423394]uncertain significance16284149162841491Humanname
407503935CV3484795single nucleotide variantNM_032852.4(ATG4C):c.1352G>A (p.Ser451Asn)not specified [RCV004670386]uncertain significance16286413462864134Humanname
597755977CV3602833single nucleotide variantNM_032852.4(ATG4C):c.1081C>T (p.Pro361Ser)not specified [RCV004868155]uncertain significance16283484462834844Humanname
598169448CV3918348single nucleotide variantNM_032852.4(ATG4C):c.1216A>C (p.Lys406Gln)not specified [RCV005284278]uncertain significance16286399862863998Humanname