CPAMD8 c.267+713G>T

Variant ID: 19-17130428-C-A

NM_015692.2(CPAMD8):c.267+713G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Single-cell Atlas of common variable immunodeficiency shows germinal center-associated epigenetic dysregulation in B-cell responses.

Nature Communications
Rodríguez-Ubreva, Javier J; Arutyunyan, Anna A; Bonder, Marc Jan MJ; Del Pino-Molina, Lucía L; Clark, Stephen J SJ; de la Calle-Fabregat, Carlos C; Garcia-Alonso, Luz L; Handfield, Louis-François LF; Ciudad, Laura L; Andrés-León, Eduardo E; Krueger, Felix F; Català-Moll, Francesc F; Rodríguez-Cortez, Virginia C VC; Polanski, Krzysztof K; Mamanova, Lira L; van Dongen, Stijn S; Kiselev, Vladimir Yu VY; Martínez-Saavedra, María T MT; Heyn, Holger H; Martín, Javier J; Warnatz, Klaus K; López-Granados, Eduardo E; Rodríguez-Gallego, Carlos C; Stegle, Oliver O; Kelsey, Gavin G; Vento-Tormo, Roser R; Ballestar, Esteban E
Publication Date: 2022-04-01

Variant appearance in text: CPAMD8: 408+713G>T
PubMed Link: 35365635
Variant Present in the following documents:
  • 41467_2022_29450_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page