CYBB c.1463C>T ;(p.A488V)

Variant ID: X-37668821-C-T

NM_000397.3(CYBB):c.1463C>T;(p.A488V)

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:

From somatic variants towards precision oncology: Evidence-driven reporting of treatment options in molecular tumor boards.

Genome Medicine
Perera-Bel, Júlia J; Hutter, Barbara B; Heining, Christoph C; Bleckmann, Annalen A; Fröhlich, Martina M; Fröhling, Stefan S; Glimm, Hanno H; Brors, Benedikt B; Beißbarth, Tim T
Publication Date: 2018-03-15

Variant appearance in text: CYBB: A488V
PubMed Link: 29544535
Variant Present in the following documents:
  • 13073_2018_529_MOESM2_ESM.xlsx, sheet 7
View BVdb publication page