ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.451del (p.Ala151fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002339985 SCV002635173 pathogenic Hereditary cancer-predisposing syndrome 2018-09-12 criteria provided, single submitter clinical testing The c.451delG variant, located in coding exon 5 of the PTEN gene, results from a deletion of one nucleotide at nucleotide position 451, causing a translational frameshift with a predicted alternate stop codon (p.A151Pfs*2). This alteration is expected to result in loss of function by premature protein truncation or nonsense-mediated mRNA decay. As such, this alteration is interpreted as a disease-causing mutation.

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