EGFR c.494_495delinsAT ;(p.R165H)

Variant ID: 7-55214368-GG-AT

NM_005228.3(EGFR):c.494_495delinsAT;(p.R165H)

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:

Identification of pathogenic missense mutations using protein stability predictors.

Scientific Reports
Gerasimavicius, Lukas L; Liu, Xin X; Marsh, Joseph A JA
Publication Date: 2020-09-21

Variant appearance in text: EGFR: R165H
PubMed Link: 32958805
Variant Present in the following documents:
  • 41598_2020_72404_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page


ProKinO: a unified resource for mining the cancer kinome.

Human Mutation
McSkimming, Daniel Ian DI; Dastgheib, Shima S; Talevich, Eric E; Narayanan, Anish A; Katiyar, Samiksha S; Taylor, Susan S SS; Kochut, Krys K; Kannan, Natarajan N
Publication Date: 2015-02

Variant appearance in text: EGFR: R165H
PubMed Link: 25382819
Variant Present in the following documents:
  • Main text
  • humu0036-0175.pdf
View BVdb publication page