ClinVar Miner

Submissions for variant NM_000321.3(RB1):c.526_532del (p.Gln176fs)

dbSNP: rs1952511865
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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 RCV001035710 SCV001199044 pathogenic Retinoblastoma 2019-03-07 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in RB1 are known to be pathogenic (PMID: 17096365). This variant has not been reported in the literature in individuals with RB1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Gln176Alafs*8) in the RB1 gene. It is expected to result in an absent or disrupted protein product.

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