Bibliome.ai browser hg19
Search
About
Stats
FAQ
EGFR c.2842G>A ;(p.V948I)
Variant ID: 7-55266550-G-A
NM_005228.3(
EGFR
):c.2842G>A;(p.V948I)
This variant was identified in 5 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Identifying potential ligand molecules EGFR mediated TNBC targeting the kinase domain-identification of customized drugs through in silico methods.
Research In Pharmaceutical Sciences
Vyshnavi, Hima H; Namboori, Krishnan K
Publication Date: 2023-04
Variant appearance in text: rs542967903
PubMed Link:
36873279
Variant Present in the following documents:
Main text
RPS-18-121.pdf
View BVdb publication page
Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.
Frontiers In Genetics
G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A
Publication Date: 2022
Variant appearance in text: rs542967903
PubMed Link:
36561320
Variant Present in the following documents:
Table2.xlsx, sheet 4
View BVdb publication page
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: V948I
PubMed Link:
32958805
Variant Present in the following documents:
41598_2020_72404_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page
Circulating tumour DNA sequence analysis as an alternative to multiple myeloma bone marrow aspirates.
Nature Communications
Kis, Olena O; Kaedbey, Rayan R; Chow, Signy S; Danesh, Arnavaz A; Dowar, Mark M; Li, Tiantian T; Li, Zhihua Z; Liu, Jessica J; Mansour, Mark M; Masih-Khan, Esther E; Zhang, Tong T; Bratman, Scott V SV; Oza, Amit M AM; Kamel-Reid, Suzanne S; Trudel, Suzanne S; Pugh, Trevor J TJ
Publication Date: 2017-05-11
Variant appearance in text: EGFR: V948I; rs542967903
PubMed Link:
28492226
Variant Present in the following documents:
ncomms15086-s3.xlsx, sheet 1
View BVdb publication page
Loss of Function of KCNC1 is associated with intellectual disability without seizures.
European Journal Of Human Genetics : Ejhg
Poirier, Karine K; Viot, Géraldine G; Lombardi, Laura L; Jauny, Clémence C; Billuart, Pierre P; Bienvenu, Thierry T
Publication Date: 2017-05
Variant appearance in text: EGFR: 2842G>A; V948I
PubMed Link:
28145425
Variant Present in the following documents:
Main text
View BVdb publication page