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PIK3CA c.679A>C ;(p.K227Q)
Variant ID: 3-178919194-A-C
NM_006218.2(
PIK3CA
):c.679A>C;(p.K227Q)
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:
A central role for PI3K-AKT signaling pathway in linking SAMHD1-deficiency to the type I interferon signature.
Scientific Reports
Oh, Changhoon C; Ryoo, Jeongmin J; Park, Kiwon K; Kim, Baek B; Daly, Michele B MB; Cho, DongYeon D; Ahn, Kwangseog K
Publication Date: 2018-01-08
Variant appearance in text: PI3K: K227Q
PubMed Link:
29311560
Variant Present in the following documents:
Main text
41598_2017_Article_18308.pdf
View BVdb publication page
Pervasive translational regulation of the cell signalling circuitry underlies mammalian development.
Nature Communications
Fujii, Kotaro K; Shi, Zhen Z; Zhulyn, Olena O; Denans, Nicolas N; Barna, Maria M
Publication Date: 2017-02-14
Variant appearance in text: PI3K: K227Q
PubMed Link:
28195124
Variant Present in the following documents:
Main text
View BVdb publication page