CUX1 c.35A>C ;(p.E12A)

Variant ID: 7-101559399-A-C

NM_181552.3(CUX1):c.35A>C;(p.E12A)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Modeling genetic epileptic encephalopathies using brain organoids.

Embo Molecular Medicine
Steinberg, Daniel J DJ; Repudi, Srinivasarao S; Saleem, Afifa A; Kustanovich, Irina I; Viukov, Sergey S; Abudiab, Baraa B; Banne, Ehud E; Mahajnah, Muhammad M; Hanna, Jacob H JH; Stern, Shani S; Carlen, Peter L PL; Aqeilan, Rami I RI
Publication Date: 2021-08-09

Variant appearance in text: CUX1: E12A
PubMed Link: 34268881
Variant Present in the following documents:
  • Main text
View BVdb publication page