ClinVar Miner

Submissions for variant NM_198576.4(AGRN):c.5908A>G (p.Asn1970Asp)

dbSNP: rs1473312060
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000651384 SCV000773235 uncertain significance Congenital myasthenic syndrome 8 2022-06-27 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 541176). This variant has not been reported in the literature in individuals affected with AGRN-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.001%). This sequence change replaces asparagine, which is neutral and polar, with aspartic acid, which is acidic and polar, at codon 1970 of the AGRN protein (p.Asn1970Asp).
Revvity Omics, Revvity Omics RCV000651384 SCV003823033 uncertain significance Congenital myasthenic syndrome 8 2021-06-07 criteria provided, single submitter clinical testing

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