ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.210_211insAGGGGCCGGCA (p.Gly71fs)

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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 RCV003176400 SCV003855798 pathogenic Hereditary cancer-predisposing syndrome 2022-11-01 criteria provided, single submitter clinical testing The c.210_211ins11 variant, located in coding exon 1 of the MSH2 gene, results from an insertion of 11 nucleotides at position 210, causing a translational frameshift with a predicted alternate stop codon (p.G71Rfs*17). 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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