CYBB c.1364C>A ;(p.A455E)

Variant ID: X-37665689-C-A

NM_000397.3(CYBB):c.1364C>A;(p.A455E)

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

.

Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
Publication Date: 2002

Variant appearance in text: CGD: A455E
PubMed Link: 32226145
Variant Present in the following documents:
  • 112_2002_Article_1.pdf
View BVdb publication page


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: CYBB: A455E
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page