ClinVar Miner

Submissions for variant NM_006269.2(RP1):c.830_831del (p.Ser277fs)

dbSNP: rs1585561400
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003718298 SCV004509404 pathogenic not provided 2023-01-30 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Ser277Cysfs*4) in the RP1 gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 1880 amino acid(s) of the RP1 protein. For these reasons, this variant has been classified as Pathogenic. This variant disrupts the C-terminus of the RP1 protein. Many variants that disrupt this region have been reported in individuals with either autosomal dominant or autosomal recessive retinitis pigmentosa (PMID: 11527933, 19933189, 29425069, 30027431, 33681214). Therefore, variants that disrupt this region are expected to be disease-causing. ClinVar contains an entry for this variant (Variation ID: 636201). This premature translational stop signal has been observed in individual(s) with retinitis pigmentosa (PMID: 30718709). This variant is not present in population databases (gnomAD no frequency).
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet RCV000787881 SCV000926897 likely pathogenic Retinitis pigmentosa 2018-04-01 no assertion criteria provided research

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