ClinVar Miner

Submissions for variant NM_001401501.2(MUC16):c.39544C>T (p.Arg13182Trp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003421801 SCV004146568 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing MUC16: BP4, BS2
PreventionGenetics, part of Exact Sciences RCV003929100 SCV004754544 benign MUC16-related disorder 2019-07-19 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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