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24 records found for search term Krtap2-4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156156968CV2266255single nucleotide variantNM_033184.4(KRTAP2-4):c.20G>C (p.Gly7Ala)not specified [RCV004128816]uncertain significance174106582641065826Humanname
405654073CV3265955single nucleotide variantNM_033184.4(KRTAP2-4):c.46G>A (p.Gly16Arg)not specified [RCV004414853]uncertain significance174106580041065800Humanname
156219984CV2254110single nucleotide variantNM_033184.4(KRTAP2-4):c.155G>A (p.Arg52His)not specified [RCV004129551]uncertain significance174106569141065691Humanname
156274388CV2316372single nucleotide variantNM_033184.4(KRTAP2-4):c.245C>T (p.Ser82Leu)not specified [RCV004169875]uncertain significance174106560141065601Humanname
156354048CV2324198single nucleotide variantNM_033184.4(KRTAP2-4):c.275G>A (p.Cys92Tyr)not specified [RCV004176940]uncertain significance174106557141065571Humanname
156293954CV2336623single nucleotide variantNM_033184.4(KRTAP2-4):c.197C>A (p.Pro66His)not specified [RCV004196868]uncertain significance174106564941065649Humanname
401772745CV2712885single nucleotide variantNM_033184.4(KRTAP2-4):c.238T>A (p.Cys80Ser)not specified [RCV004314293]uncertain significance174106560841065608Humanname
401772764CV2712896single nucleotide variantNM_033184.4(KRTAP2-4):c.240C>G (p.Cys80Trp)not specified [RCV004314301]uncertain significance174106560641065606Humanname
401778240CV2712904single nucleotide variantNM_033184.4(KRTAP2-4):c.241C>A (p.Pro81Thr)not specified [RCV004314307]uncertain significance174106560541065605Humanname
405654062CV3265951single nucleotide variantNM_033184.4(KRTAP2-4):c.140T>C (p.Val47Ala)not specified [RCV004414849]uncertain significance174106570641065706Humanname
405654067CV3265953single nucleotide variantNM_033184.4(KRTAP2-4):c.151A>G (p.Thr51Ala)not specified [RCV004414851]uncertain significance174106569541065695Humanname
407480321CV3445791single nucleotide variantNM_033184.4(KRTAP2-4):c.191G>A (p.Cys64Tyr)not specified [RCV004639713]uncertain significance174106565541065655Humanname
597624947CV3695981single nucleotide variantNM_033184.4(KRTAP2-4):c.116C>T (p.Thr39Ile)not specified [RCV004937896]uncertain significance174106573041065730Humanname
597624925CV3695982single nucleotide variantNM_033184.4(KRTAP2-4):c.257C>T (p.Ala86Val)not specified [RCV004937897]uncertain significance174106558941065589Humanname
597624904CV3695983single nucleotide variantNM_033184.4(KRTAP2-4):c.179G>A (p.Arg60His)not specified [RCV004937898]uncertain significance174106566741065667Humanname
598173124CV3991268single nucleotide variantNM_033184.4(KRTAP2-4):c.283G>A (p.Ala95Thr)not specified [RCV005370879]uncertain significance174106556341065563Humanname
329349542CV2438946single nucleotide variantNM_033184.4(KRTAP2-4):c.323G>A (p.Cys108Tyr)not specified [RCV004264462]uncertain significance174106552341065523Humanname
401860712CV2758590single nucleotide variantNM_033184.4(KRTAP2-4):c.360C>A (p.Ser120Arg)not specified [RCV004337675]likely benign174106548641065486Humanname
405654070CV3265954single nucleotide variantNM_033184.4(KRTAP2-4):c.368G>A (p.Cys123Tyr)not specified [RCV004414852]uncertain significance174106547841065478Humanname
597795096CV3695977single nucleotide variantNM_033184.4(KRTAP2-4):c.377C>A (p.Ser126Tyr)not specified [RCV004934757]uncertain significance174106546941065469Humanname
597624972CV3695978single nucleotide variantNM_033184.4(KRTAP2-4):c.340G>C (p.Gly114Arg)not specified [RCV004937893]uncertain significance174106550641065506Humanname
597624949CV3695979single nucleotide variantNM_033184.4(KRTAP2-4):c.331C>A (p.Pro111Thr)not specified [RCV004937894]uncertain significance174106551541065515Humanname
598196330CV3991267single nucleotide variantNM_033184.4(KRTAP2-4):c.314A>G (p.Gln105Arg)not specified [RCV005355167]uncertain significance174106553241065532Humanname
598196337CV3991269single nucleotide variantNM_033184.4(KRTAP2-4):c.347C>G (p.Pro116Arg)not specified [RCV005355168]uncertain significance174106549941065499Humanname