ClinVar Miner

Submissions for variant NM_000506.5(F2):c.1156C>A (p.Pro386Thr)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Skane University Hospital Lund RCV004697592 SCV005197846 uncertain significance not provided 2024-02-20 criteria provided, single submitter clinical testing
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV005002039 SCV005627710 uncertain significance Congenital prothrombin deficiency 2024-07-23 criteria provided, single submitter clinical testing

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