Bibliome.ai browser hg19
Search
About
Stats
FAQ
EGF c.2114C>T ;(p.P705L)
Variant ID: 4-110901188-C-T
NM_001963.4(
EGF
):c.2114C>T;(p.P705L)
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:
Functional characterization of human cancer-derived TRKB mutations.
Plos One
Geiger, Thomas R TR; Song, Ji-Ying JY; Rosado, Aranzazu A; Peeper, Daniel S DS
Publication Date: 2011-02-17
Variant appearance in text: EGF: P705L
PubMed Link:
21379385
Variant Present in the following documents:
Main text
pone.0016871.pdf
View BVdb publication page