F2 c.922G>A ;(p.D308N)

Variant ID: 11-46748095-G-A

NM_000506.3(F2):c.922G>A;(p.D308N)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Vanishing white matter: Eukaryotic initiation factor 2B model and the impact of missense mutations.

Molecular Genetics & Genomic Medicine
Slynko, Inna I; Nguyen, Stephanie S; Hamilton, Eline M C EMC; Wisse, Lisanne E LE; de Esch, Iwan J P IJP; de Graaf, Chris C; Bruning, John B JB; Proud, Christopher G CG; Abbink, Truus E M TEM; van der Knaap, Marjo S MS
Publication Date: 2021-03

Variant appearance in text: F2: 922G>A
PubMed Link: 33432707
Variant Present in the following documents:
  • MGG3-9-e1593-s001.pdf
View BVdb publication page