ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.458A>C (p.Tyr153Ser)

dbSNP: rs769827245
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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 RCV000696162 SCV000824710 uncertain significance DICER1-related tumor predisposition 2020-08-05 criteria provided, single submitter clinical testing This sequence change replaces tyrosine with serine at codon 153 of the DICER1 protein (p.Tyr153Ser). The tyrosine residue is weakly conserved and there is a large physicochemical difference between tyrosine and serine. 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 output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The serine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with DICER1-related disease. This variant is not present in population databases (ExAC no frequency).

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