EGFR c.890-347G>A

Variant ID: 7-55223176-G-A

NM_005228.3(EGFR):c.890-347G>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs6950826
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Epigenetic and genomic profiling of chordoid meningioma: implications for clinical management.

Acta Neuropathologica Communications
Daoud, Elena V EV; Zhu, Kelsey K; Mickey, Bruce B; Mohamed, Hussein H; Wen, Mandisa M; Delorenzo, Michael M; Tran, Ivy I; Serrano, Jonathan J; Hatanpaa, Kimmo J KJ; Raisanen, Jack M JM; Snuderl, Matija M; Cai, Chunyu C
Publication Date: 2022-04-19

Variant appearance in text: EGFR: 890-347G>A; rs6950826
PubMed Link: 35440040
Variant Present in the following documents:
  • 40478_2022_1362_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: EGFR: 890-347G>A; rs6950826
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs6950826
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



EGFR and SYNE2 are associated with p21 expression and SYNE2 variants predict post-operative clinical outcomes in HBV-related hepatocellular carcinoma.

Scientific Reports
Han, Chuangye C; Liao, Xiwen X; Qin, Wei W; Yu, Long L; Liu, Xiaoguang X; Chen, Gang G; Liu, Zhengtao Z; Lu, Sicong S; Chen, Zhiwei Z; Su, Hao H; Zhu, Guangzhi G; Lu, Zili Z; Liu, Zhiming Z; Qin, Xue X; Gui, Ying Y; Mo, Zengnan Z; Li, Lequn L; Peng, Tao T
Publication Date: 2016-08-09

Variant appearance in text: rs6950826
PubMed Link: 27502069
Variant Present in the following documents:
  • Main text
  • srep31237.pdf
View BVdb publication page



Genome-wide association study identified PLCE1- rs2797992 and EGFR- rs6950826 were associated with TP53 expression in the HBV-related hepatocellular carcinoma of Chinese patients in Guangxi.

American Journal Of Translational Research
Liao, Xiwen X; Han, Chuangye C; Qin, Wei W; Liu, Xiaoguang X; Yu, Long L; Lu, Sicong S; Chen, Zhiwei Z; Zhu, Guangzhi G; Su, Hao H; Mo, Zengnan Z; Qin, Xue X; Peng, Tao T
Publication Date: 2016

Variant appearance in text: rs6950826
PubMed Link: 27186304
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of novel SNPs in glioblastoma using targeted resequencing.

Plos One
Keller, Andreas A; Harz, Christian C; Matzas, Mark M; Meder, Benjamin B; Katus, Hugo A HA; Ludwig, Nicole N; Fischer, Ulrike U; Meese, Eckart E
Publication Date: 2011

Variant appearance in text: rs6950826
PubMed Link: 21695249
Variant Present in the following documents:
  • pone.0018158.s001.xls, sheet 4
View BVdb publication page