ClinVar Miner

Submissions for variant NM_001122769.3(LCA5):c.10A>G (p.Arg4Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV005208359 SCV005849368 uncertain significance Leber congenital amaurosis 5 2023-06-22 criteria provided, single submitter clinical testing The missense c.10A>G(p.Arg4Gly) variant in LCA5 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Arg4Gly variant is absent in gnomAD Exomes. This variant has not been submitted to the ClinVar database. Multiple lines of computational evidence (Polyphen - Probably Damaging, SIFT - Damaging and MutationTaster - Disease causing) predict damaging effect on protein structure and function for this variant. The reference amino acid at this position in LCA5 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Arg at position 4 is changed to a Gly changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as Variant of Uncertain Significance (VUS).

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