ClinVar Miner

Submissions for variant NM_012222.2(MUTYH):c.881G>T (p.Cys294Phe) (rs879254257)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000502805 SCV000592701 uncertain significance Carcinoma of colon no assertion criteria provided clinical testing The p.Cys297Phe variant has not been reported in the literature nor previously identified by our laboratory. The Cys residue is conserved across mammals and computational analyses (PolyPhen2, SIFT, AlignGVGD) suggest that the Phe variant may impact the protein. However, this information is not predictive enough to assume pathogenicity. The presence of this variant in combination with a reported pathogenic variant increases the likelihood that the p.Cys297Phe variant is pathogenic. In summary, based on the above information, the clinical significance of this variant cannot be determined with certainty at this time although we would lean towards a more pathogenic role for this variant. This variant is classified as a Predicted Pathogenic.

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