EGFR c.2248G>A ;(p.A750T)

Variant ID: 7-55242478-G-A

NM_005228.3(EGFR):c.2248G>A;(p.A750T)

This variant was identified in 1 publication

View GRCh38 version.



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

Publications:

Gene mutations in stool from gastric and colorectal neoplasia patients by next-generation sequencing.

World Journal Of Gastroenterology
Youssef, Omar O; Sarhadi, Virinder V; Ehsan, Homa H; Böhling, Tom T; Carpelan-Holmström, Monika M; Koskensalo, Selja S; Puolakkainen, Pauli P; Kokkola, Arto A; Knuutila, Sakari S
Publication Date: 2017-12-21

Variant appearance in text: EGFR: A750T
PubMed Link: 29307989
Variant Present in the following documents:
  • Main text
  • WJG-23-8291.pdf
View BVdb publication page