ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1245_1246dup (p.Asn416fs)

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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 RCV002391583 SCV002668929 pathogenic Hereditary cancer-predisposing syndrome 2019-04-02 criteria provided, single submitter clinical testing The c.1245_1246dupTA pathogenic mutation, located in coding exon 7 of the MSH2 gene, results from a duplication of TA at nucleotide position 1245, causing a translational frameshift with a predicted alternate stop codon (p.N416Ifs*23). 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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