ClinVar Miner

Submissions for variant NM_198576.4(AGRN):c.5132C>A (p.Ala1711Glu)

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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 RCV004577207 SCV005061117 uncertain significance Congenital myasthenic syndrome 8 criteria provided, single submitter clinical testing The observed missense c.5132C>A (p.Ala1711Glu) variant in AGRN gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Ala1711Glu variant is absent in gnomAD exomes database. This variant has not been submitted to the ClinVar database. The amino acid change p.Ala1711Glu in AGRN is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Ala at position 1711 is changed to a Glu changing protein sequence and it might alter its composition and physico-chemical properties. Multiple lines of computational evidence predicts damaging effect on protein structure and function for this variant (Sift - Damaging; Mutation Taster - disease_causing). Additional studies will be required to prove the pathogenicity of this variant. For these reasons, this variant has been classified as a Variant of Uncertain Significance (VUS).

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