ClinVar Miner

Submissions for variant NM_000321.3(RB1):c.80C>G (p.Pro27Arg)

gnomAD frequency: 0.00003  dbSNP: rs925399787
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001213879 SCV001385531 likely benign Retinoblastoma 2024-01-05 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256701 SCV002530864 uncertain significance Hereditary cancer-predisposing syndrome 2021-07-02 criteria provided, single submitter curation
Ambry Genetics RCV002256701 SCV002677115 likely benign Hereditary cancer-predisposing syndrome 2023-03-03 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
All of Us Research Program, National Institutes of Health RCV001213879 SCV004846304 uncertain significance Retinoblastoma 2023-09-04 criteria provided, single submitter clinical testing This missense variant replaces proline with arginine at codon 27 of the RB1 protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with RB1-related disorders in the literature. This variant has been identified in 1/31284 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

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