ClinVar Miner

Submissions for variant NM_000321.3(RB1):c.656T>C (p.Met219Thr)

dbSNP: rs1952625561
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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 RCV001060902 SCV001225622 uncertain significance Retinoblastoma 2019-12-06 criteria provided, single submitter clinical testing 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: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C45"). This variant has been reported in an individual with unilateral retinoblastoma in the Leiden Open-source Variation Database (PMID: 21520333). This variant is not present in population databases (ExAC no frequency). This sequence change replaces methionine with threonine at codon 219 of the RB1 protein (p.Met219Thr). The methionine residue is moderately conserved and there is a moderate physicochemical difference between methionine and threonine.

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