ClinVar Miner

Submissions for variant NM_020366.4(RPGRIP1):c.1238T>G (p.Leu413Arg)

gnomAD frequency: 0.00001  dbSNP: rs1486475994
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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 RCV001911593 SCV002175443 uncertain significance Cone-rod dystrophy 13; Leber congenital amaurosis 6 2022-07-05 criteria provided, single submitter clinical testing This sequence change replaces leucine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 413 of the RPGRIP1 protein (p.Leu413Arg). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive. ClinVar contains an entry for this variant (Variation ID: 1401004). This variant has not been reported in the literature in individuals affected with RPGRIP1-related conditions. This variant is not present in population databases (gnomAD no frequency).

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