ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.967_968dup (p.Asn323fs)

dbSNP: rs121913291
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001192923 SCV001361383 likely pathogenic Cowden syndrome 2019-02-19 criteria provided, single submitter clinical testing Variant summary: PTEN c.967_968dupAA (p.Asn323LysfsX22) results in a premature termination codon, predicted to cause a truncation of the encoded protein or absence of the protein due to nonsense mediated decay, which are commonly known mechanisms for disease. The variant was absent in 246006 control chromosomes (gnomAD). To our knowledge, no occurrence of c.967_968dupAA in individuals affected with Cowden Syndrome and no experimental evidence demonstrating its impact on protein function have been reported. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014. Based on the evidence outlined above, the variant was classified as likely pathogenic.

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