ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.1238C>G (p.Thr413Arg)

dbSNP: rs63750766
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001010494 SCV001170701 uncertain significance Hereditary cancer-predisposing syndrome 2019-09-16 criteria provided, single submitter clinical testing The p.T413R variant (also known as c.1238C>G), located in coding exon 12 of the MLH1 gene, results from a C to G substitution at nucleotide position 1238. The threonine at codon 413 is replaced by arginine, an amino acid with similar properties. This amino acid position is poorly conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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