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EGFR c.1390T>G ;(p.S464A)
Variant ID: 7-55227923-T-G
NM_005228.3(
EGFR
):c.1390T>G;(p.S464A)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
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: EGFR: S464A
PubMed Link:
36561320
Variant Present in the following documents:
Table3.xlsx, sheet 1
Table2.xlsx, sheet 4
View BVdb publication page
Genetic profiling of somatic alterations by Oncomine Focus Assay in Korean patients with advanced gastric cancer.
Oncology Letters
Park, Joonhong J; Lee, Sang-Il SI; Shin, Soyoung S; Hong, Jang Hee JH; Yoo, Han Mo HM; Kim, Jeong Goo JG
Publication Date: 2020-11
Variant appearance in text: EGFR: 1390T>G; Ser464Ala
PubMed Link:
32934698
Variant Present in the following documents:
Main text
ol-20-05-11990.pdf
View BVdb publication page