PIK3CB c.539A>G ;(p.H180R)

Variant ID: 3-138461482-T-C

NM_006219.2(PIK3CB):c.539A>G;(p.H180R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Integrating Genomics and Clinical Data for Statistical Analysis by Using GEnome MINIng (GEMINI) and Fast Healthcare Interoperability Resources (FHIR): System Design and Implementation.

Journal Of Medical Internet Research
Gruendner, Julian J; Wolf, Nicolas N; Tögel, Lars L; Haller, Florian F; Prokosch, Hans-Ulrich HU; Christoph, Jan J
Publication Date: 2020-10-07

Variant appearance in text: PIK3CB: 539A>G
PubMed Link: 33026356
Variant Present in the following documents:
  • Main text
View BVdb publication page