ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.244C>T (p.Gln82Ter)

gnomAD frequency: 0.00001  dbSNP: rs372763743
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001303540 SCV001492788 uncertain significance Colorectal cancer, hereditary nonpolyposis, type 7 2020-03-04 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. The current clinical and genetic evidence is not sufficient to establish whether loss-of-function variants in MLH3 cause disease. This variant has not been reported in the literature in individuals with MLH3-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Gln82*) in the MLH3 gene. It is expected to result in an absent or disrupted protein product.
Fulgent Genetics, Fulgent Genetics RCV005005146 SCV005633330 uncertain significance Endometrial carcinoma; Colorectal cancer, hereditary nonpolyposis, type 7; Colorectal cancer 2024-04-24 criteria provided, single submitter clinical testing

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