PIK3CA c.1286T>G ;(p.L429W)

Variant ID: 3-178928008-T-G

NM_006218.2(PIK3CA):c.1286T>G;(p.L429W)

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:

Advances in understanding the pathogenesis of primary familial and congenital polycythaemia.

British Journal Of Haematology
Huang, Lily J LJ; Shen, Yu-Min YM; Bulut, Gamze B GB
Publication Date: 2010-03

Variant appearance in text: PI3K: L429W
PubMed Link: 20096014
Variant Present in the following documents:
  • Main text
View BVdb publication page