ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1361_1364del (p.Ile454fs)

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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 RCV002383494 SCV002698277 pathogenic Hereditary cancer-predisposing syndrome 2018-03-05 criteria provided, single submitter clinical testing The c.1361_1364delTAGA pathogenic mutation, located in coding exon 8 of the MSH2 gene, results from a deletion of 4 nucleotides at nucleotide positions 1361 to 1364, causing a translational frameshift with a predicted alternate stop codon (p.I454Kfs*4). 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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