EGFR c.1489_1490delinsGC ;(p.N497A)

Variant ID: 7-55228022-AA-GC

NM_005228.3(EGFR):c.1489_1490delinsGC;(p.N497A)

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:

Mitigating off-target effects in CRISPR/Cas9-mediated in vivo gene editing.

Journal Of Molecular Medicine (Berlin, Germany)
Han, Hua Alexander HA; Pang, Jeremy Kah Sheng JKS; Soh, Boon-Seng BS
Publication Date: 2020-05

Variant appearance in text: EGFR: N497A
PubMed Link: 32198625
Variant Present in the following documents:
  • Main text
  • 109_2020_Article_1893.pdf
View BVdb publication page