ClinVar Miner

Submissions for variant NM_201253.3(CRB1):c.2767G>T (p.Glu923Ter)

dbSNP: rs2125489019
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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 RCV001382442 SCV001581214 pathogenic Retinitis pigmentosa 12; Leber congenital amaurosis 8 2022-03-10 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Glu923*) in the CRB1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in CRB1 are known to be pathogenic (PMID: 10508521, 22065545, 23379534, 25412400, 26957898, 28041643, 29391521). For these reasons, this variant has been classified as Pathogenic. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. ClinVar contains an entry for this variant (Variation ID: 1070332). This variant has not been reported in the literature in individuals affected with CRB1-related conditions. This variant is not present in population databases (gnomAD no frequency).

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