ClinVar Miner

Submissions for variant NM_002905.5(RDH5):c.218C>T (p.Ser73Phe)

dbSNP: rs62638185
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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 RCV001851737 SCV002181664 uncertain significance not provided 2023-11-20 criteria provided, single submitter clinical testing This sequence change replaces serine, which is neutral and polar, with phenylalanine, which is neutral and non-polar, at codon 73 of the RDH5 protein (p.Ser73Phe). This variant is present in population databases (rs62638185, gnomAD no frequency). This missense change has been observed in individual(s) with fundus albipunctatus (PMID: 10369264). In at least one individual the data is consistent with being in trans (on the opposite chromosome) from a pathogenic variant. ClinVar contains an entry for this variant (Variation ID: 8004). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt RDH5 protein function with a positive predictive value of 80%. Experimental studies have shown that this missense change affects RDH5 function (PMID: 11675386). 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.
OMIM RCV000008468 SCV000028676 pathogenic Fundus albipunctatus, autosomal recessive 1999-06-01 no assertion criteria provided literature only

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