ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.1123C>G (p.Pro375Ala)

dbSNP: rs1595439411
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001213430 SCV001385059 uncertain significance DICER1-related tumor predisposition 2019-06-30 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with DICER1-related conditions. 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. 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 C0"). This variant is not present in population databases (ExAC no frequency). This sequence change replaces proline with alanine at codon 375 of the DICER1 protein (p.Pro375Ala). The proline residue is highly conserved and there is a small physicochemical difference between proline and alanine.

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