ClinVar Miner

Submissions for variant NM_002334.4(LRP4):c.4369C>G (p.Leu1457Val)

gnomAD frequency: 0.00001  dbSNP: rs571418643
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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 RCV001916961 SCV002193167 uncertain significance Cenani-Lenz syndactyly syndrome; Sclerosteosis 2; Congenital myasthenic syndrome 17 2022-08-09 criteria provided, single submitter clinical testing 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: 1421527). This variant has not been reported in the literature in individuals affected with LRP4-related conditions. This variant is present in population databases (rs571418643, gnomAD 0.0009%). This sequence change replaces leucine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 1457 of the LRP4 protein (p.Leu1457Val).

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