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EGFR c.655T>G ;(p.C219G)
Variant ID: 7-55220265-T-G
NM_005228.3(
EGFR
):c.655T>G;(p.C219G)
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:
Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows.
Bmc Medical Genomics
Sobahy, Turki M TM; Tashkandi, Ghassan G; Bahussain, Donya D; Al-Harbi, Raneem R
Publication Date: 2022-04-25
Variant appearance in text: EGFR: 655T>G
PubMed Link:
35468810
Variant Present in the following documents:
12920_2022_1235_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
Analysis on GENIE reveals novel recurrent variants that affect molecular diagnosis of sizable number of cancer patients.
Bmc Cancer
Koyama, Takahiko T; Rhrissorrakrai, Kahn K; Parida, Laxmi L
Publication Date: 2019-02-01
Variant appearance in text: EGFR: 655T>G; C219G
PubMed Link:
30709382
Variant Present in the following documents:
12885_2019_5313_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
CanDrA: cancer-specific driver missense mutation annotation with optimized features.
Plos One
Mao, Yong Y; Chen, Han H; Liang, Han H; Meric-Bernstam, Funda F; Mills, Gordon B GB; Chen, Ken K
Publication Date: 2013
Variant appearance in text: EGFR: C219G
PubMed Link:
24205039
Variant Present in the following documents:
pone.0077945.s001.xls, sheet 11
View BVdb publication page