ClinVar Miner

Submissions for variant NM_020366.4(RPGRIP1):c.1687C>T (p.Arg563Ter)

dbSNP: rs776963292
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002537617 SCV003512990 pathogenic Cone-rod dystrophy 13; Leber congenital amaurosis 6 2022-04-24 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Arg563*) in the RPGRIP1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in RPGRIP1 are known to be pathogenic (PMID: 11528500, 23105016). This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with Leber congenital amaurosis (PMID: 29844330). ClinVar contains an entry for this variant (Variation ID: 981641). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. For these reasons, this variant has been classified as Pathogenic.
Laboratory of Genetics in Ophthalmology, Institut Imagine RCV001261181 SCV001438580 pathogenic Leber congenital amaurosis 6 no assertion criteria provided research

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