ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.1028G>C (p.Gly343Ala)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005007304 SCV005633317 uncertain significance Endometrial carcinoma; Colorectal cancer, hereditary nonpolyposis, type 7; Colorectal cancer 2024-01-24 criteria provided, single submitter clinical testing

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