ClinVar Miner

Submissions for variant NM_052859.4(RFT1):c.271C>T (p.Pro91Ser)

gnomAD frequency: 0.00001  dbSNP: rs147915986
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002020877 SCV002297538 uncertain significance RFT1-congenital disorder of glycosylation 2022-07-11 criteria provided, single submitter clinical testing This sequence change replaces proline, which is neutral and non-polar, with serine, which is neutral and polar, at codon 91 of the RFT1 protein (p.Pro91Ser). This variant is present in population databases (rs147915986, gnomAD 0.007%). This variant has not been reported in the literature in individuals affected with RFT1-related conditions. ClinVar contains an entry for this variant (Variation ID: 1515148). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C15"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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