WARS2 c.622G>T ;(p.E208*)

Variant ID: 1-119576730-C-A

NM_015836.3(WARS2):c.622G>T;(p.E208*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant.

Genes
Pauly, Martje G MG; Korenke, G Christoph GC; Diaw, Sokhna Haissatou SH; Grözinger, Anne A; Cazurro-Gutiérrez, Ana A; Pérez-Dueñas, Belén B; González, Victoria V; Macaya, Alfons A; Serrano Antón, Ana Teresa AT; Peterlin, Borut B; Božović, Ivana Babić IB; Maver, Aleš A; Münchau, Alexander A; Lohmann, Katja K
Publication Date: 2023-03-29

Variant appearance in text: WARS2: 622G>T; Glu208Ter
PubMed Link: 37107582
Variant Present in the following documents:
  • genes-14-00822.pdf
View BVdb publication page