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Variants search result for Homo sapiens
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7 records found for search term Pcp4l1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15153374CV778742single nucleotide variantNM_001102566.2(PCP4L1):c.64+9G>Tnot provided [RCV000968532]benign1161283731161283731Humanname
15185516CV696218single nucleotide variantNM_001102566.2(PCP4L1):c.192G>A (p.Lys64=)not provided [RCV000953007]benign1161284466161284466Humanname
156107141CV2355304single nucleotide variantNM_001102566.2(PCP4L1):c.89C>T (p.Ala30Val)not specified [RCV004203154]uncertain significance1161284363161284363Humanname
597697523CV3571944single nucleotide variantNM_001102566.2(PCP4L1):c.92A>C (p.Glu31Ala)not specified [RCV004839337]uncertain significance1161284366161284366Humanname
156326199CV2335427single nucleotide variantNM_001102566.2(PCP4L1):c.169C>T (p.Arg57Trp)not specified [RCV004186976]uncertain significance1161284443161284443Humanname
405762446CV3364834single nucleotide variantNM_001102566.2(PCP4L1):c.170G>A (p.Arg57Gln)not specified [RCV004500849]uncertain significance1161284444161284444Humanname
598165096CV4006024single nucleotide variantNM_001102566.2(PCP4L1):c.158A>G (p.Gln53Arg)not specified [RCV005391273]uncertain significance1161284432161284432Humanname