ClinVar Miner

Submissions for variant NM_004329.3(BMPR1A):c.642A>G (p.Gln214=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004791965 SCV005405230 benign Juvenile polyposis syndrome 2024-08-01 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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