ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1024del (p.Val342fs)

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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 RCV002380541 SCV002691376 pathogenic Hereditary cancer-predisposing syndrome 2021-02-17 criteria provided, single submitter clinical testing The c.1024delG pathogenic mutation, located in coding exon 6 of the MSH2 gene, results from a deletion of one nucleotide at nucleotide position 1024, causing a translational frameshift with a predicted alternate stop codon (p.V342Lfs*15). This alteration is expected to result in loss of function by premature protein truncation or nonsense-mediated mRNA decay. As such, this alteration is interpreted as a disease-causing mutation.

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