KCNQ1 c.1489C>T ;(p.L497=)

Variant ID: 11-2683286-C-T

NM_000218.2(KCNQ1):c.1489C>T;(p.L497=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms.

Molecular Autism
Trelles, M Pilar MP; Levy, Tess T; Lerman, Bonnie B; Siper, Paige P; Lozano, Reymundo R; Halpern, Danielle D; Walker, Hannah H; Zweifach, Jessica J; Frank, Yitzchak Y; Foss-Feig, Jennifer J; Kolevzon, Alexander A; Buxbaum, Joseph J
Publication Date: 2021-09-29

Variant appearance in text: KCNQ1: 1489C>T
PubMed Link: 34588003
Variant Present in the following documents:
  • 13229_2021_469_MOESM1_ESM.pdf
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