ClinVar Miner

Submissions for variant NM_014141.6(CNTNAP2):c.1252A>G (p.Asn418Asp)

gnomAD frequency: 0.00001  dbSNP: rs772179690
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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 RCV000815499 SCV000955957 uncertain significance Cortical dysplasia-focal epilepsy syndrome 2022-09-01 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. Experimental studies have shown that this missense change does not substantially affect CNTNAP2 function (PMID: 22872700, 29788201). Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The aspartic acid amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. ClinVar contains an entry for this variant (Variation ID: 658643). This missense change has been observed in individual(s) with autism spectrum disorder (ASD) (PMID: 18179895). This variant is present in population databases (rs772179690, gnomAD 0.0009%). This sequence change replaces asparagine, which is neutral and polar, with aspartic acid, which is acidic and polar, at codon 418 of the CNTNAP2 protein (p.Asn418Asp).

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