ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.718T>C (p.Phe240Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005398398 SCV006055790 uncertain significance Mismatch repair cancer syndrome 1; Muir-Torré syndrome; Colorectal cancer, hereditary nonpolyposis, type 2 2024-08-20 criteria provided, single submitter clinical testing

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