EGFR c.37G>C ;(p.A13P)

Variant ID: 7-55087007-G-C

NM_005228.3(EGFR):c.37G>C;(p.A13P)

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Molecular subversion of Cdc42 signalling in cancer.

Biochemical Society Transactions
Murphy, Natasha P NP; Binti Ahmad Mokhtar, Ana Masara AM; Mott, Helen R HR; Owen, Darerca D
Publication Date: 2021-06-30

Variant appearance in text: EGFR: A13P
PubMed Link: 34196668
Variant Present in the following documents:
  • Main text
  • BST-49-1425.pdf
View BVdb publication page


Integrative omics analyses broaden treatment targets in human cancer.

Genome Medicine
Sengupta, Sohini S; Sun, Sam Q SQ; Huang, Kuan-Lin KL; Oh, Clara C; Bailey, Matthew H MH; Varghese, Rajees R; Wyczalkowski, Matthew A MA; Ning, Jie J; Tripathi, Piyush P; McMichael, Joshua F JF; Johnson, Kimberly J KJ; Kandoth, Cyriac C; Welch, John J; Ma, Cynthia C; Wendl, Michael C MC; Payne, Samuel H SH; Fenyö, David D; Townsend, Reid R RR; Dipersio, John F JF; Chen, Feng F; Ding, Li L
Publication Date: 2018-07-27

Variant appearance in text: EGFR: A13P
PubMed Link: 30053901
Variant Present in the following documents:
  • 13073_2018_564_MOESM2_ESM.xlsx, sheet 19
View BVdb publication page