EGFR c.1499-177A>G

Variant ID: 7-55229015-A-G

NM_005228.3(EGFR):c.1499-177A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


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: rs11536635
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Germline determinants of clinical outcome of cutaneous melanoma.

Pigment Cell & Melanoma Research
Vogelsang, Matjaz M; Wilson, Melissa M; Kirchhoff, Tomas T
Publication Date: 2016-01

Variant appearance in text: rs11536635
PubMed Link: 26342156
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene variants in angiogenesis and lymphangiogenesis and cutaneous melanoma progression.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Park, Jong Y JY; Amankwah, Ernest K EK; Anic, Gabriella M GM; Lin, Hui-Yi HY; Walls, Brooke B; Park, Hyun H; Krebs, Kevin K; Madden, Melissa M; Maddox, Kristen K; Marzban, Suroosh S; Fang, Shenying S; Chen, Wei W; Lee, Jeffrey E JE; Wei, Qingyi Q; Amos, Christopher I CI; Messina, Jane L JL; Sondak, Vernon K VK; Sellers, Thomas A TA; Egan, Kathleen M KM
Publication Date: 2013-05

Variant appearance in text: rs11536635
PubMed Link: 23462921
Variant Present in the following documents:
  • Main text
View BVdb publication page