ClinVar Miner

Submissions for variant NM_020822.3(KCNT1):c.2206_2211del (p.Val736_Thr737del)

dbSNP: rs781600347
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001226023 SCV001398319 uncertain significance Developmental and epileptic encephalopathy, 14; Autosomal dominant nocturnal frontal lobe epilepsy 5 2023-10-30 criteria provided, single submitter clinical testing This variant, c.2206_2211del, results in the deletion of 2 amino acid(s) of the KCNT1 protein (p.Val736_Thr737del), but otherwise preserves the integrity of the reading frame. This variant is present in population databases (rs781600347, gnomAD 0.02%). This variant has been observed in individuals with clinical features of developmental and epileptic encephalopathy (Invitae). ClinVar contains an entry for this variant (Variation ID: 953691). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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.

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