ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.*667A>T

dbSNP: rs886047409
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000337018 SCV000365757 uncertain significance PTEN hamartoma tumor syndrome 2016-06-14 criteria provided, single submitter clinical testing
Liquid Biopsy and Cancer Interception Group, Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research RCV003128616 SCV003806331 likely benign Squamous cell carcinoma 2022-06-06 criteria provided, single submitter research
Liquid Biopsy and Cancer Interception Group, Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research RCV003128615 SCV003806424 uncertain significance Lung adenocarcinoma 2022-06-06 criteria provided, single submitter research

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