ClinVar Miner

Submissions for variant NM_014000.2(VCL):c.1275T>C (p.Pro425=) (rs397517233)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000038792 SCV000062470 likely benign not specified 2012-07-30 criteria provided, single submitter clinical testing Pro425Pro in exon 10 of VCL: This variant is not expected to have clinical signi ficance because it does not alter an amino acid residue and is not located withi n the splice consensus sequence. Pro425Pro in exon 10 of VCL (allele frequency = n/a)

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