CYBB c.866G>A ;(p.W289*)

Variant ID: X-37660570-G-A

NM_000397.3(CYBB):c.866G>A;(p.W289*)

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:

Screening for primary immunodeficiency diseases by next-generation sequencing in early life.

Clinical & Translational Immunology
Sun, Jinqiao J; Yang, Lin L; Lu, Yulan Y; Wang, Huijun H; Peng, Xiaomin X; Dong, Xinran X; Cheng, Guoqiang G; Cao, Yun Y; Wu, Bingbing B; Wang, Xiaochuan X; Zhou, Wenhao W
Publication Date: 2020-05

Variant appearance in text: CYBB: 866G>A
PubMed Link: 32431812
Variant Present in the following documents:
  • CTI2-9-e1138-s001.xlsx, sheet 2
  • CTI2-9-e1138-s001.xlsx, sheet 1
View BVdb publication page