ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.1540-55C>T

gnomAD frequency: 0.04697  dbSNP: rs45455192
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001540893 SCV001758823 benign not provided 2018-07-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001540893 SCV005302477 benign not provided criteria provided, single submitter not provided
Faculté Pluridciplinaire Nador, Université Mohamed Premier RCV001250966 SCV001250949 uncertain significance Squamous cell lung carcinoma 2020-05-05 no assertion criteria provided clinical testing

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