CYBB c.1315_1316delinsTA ;(p.I439Y)

Variant ID: X-37665640-AT-TA

NM_000397.3(CYBB):c.1315_1316delinsTA;(p.I439Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: I439Y
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page