GAA c.2479_2481del ;(p.Q827del)

Variant ID: 17-78091544-TGCA-T

NM_000152.3(GAA):c.2479_2481del;(p.Q827del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A generic assay for the identification of splicing variants that induce nonsense-mediated decay in Pompe disease.

European Journal Of Human Genetics : Ejhg
Bergsma, Atze J AJ; In 't Groen, Stijn L M SLM; Catalano, Fabio F; Yamanaka, Manjiro M; Takahashi, Satoru S; Okumiya, Toshika T; van der Ploeg, Ans T AT; Pijnappel, W W M Pim WWMP
Publication Date: 2021-03

Variant appearance in text: GAA: Gln827del
PubMed Link: 33168984
Variant Present in the following documents:
  • Main text
  • 41431_2020_Article_751.pdf
View BVdb publication page