ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.255del (p.Thr86fs) (rs1064793183)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000479132 SCV000565209 pathogenic not provided 2014-11-12 criteria provided, single submitter clinical testing This deletion of one nucleotide in MSH6 is denoted c.255delC at the cDNA level and p.Thr86ProfsX63 (T86PfsX63) at the protein level. The normal sequence, with the bases that are deleted in brackets, is GCCCC[C]ACCA. The deletion causes a frameshift, which changes a Threonine to a Proline at codon 86, and creates a premature stop codon at position 63 of the new reading frame. Although this variant has not, to our knowledge, been reported in the literature, it is predicted to cause loss of normal protein function through either protein truncation or nonsense-mediated mRNA decay. we consider this variant to be pathogenic.

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