APOE c.238_240delinsTGT ;(p.A80C)

Variant ID: 19-45411791-GCG-TGT

NM_000041.2(APOE):c.238_240delinsTGT;(p.A80C)

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:

Robust Sampling of Defective Pathways in Alzheimer's Disease. Implications in Drug Repositioning.

International Journal Of Molecular Sciences
Fernández-Martínez, Juan Luis JL; Álvarez-Machancoses, Óscar Ó; de Andrés-Galiana, Enrique J EJ; Bea, Guillermina G; Kloczkowski, Andrzej A
Publication Date: 2020-05-19

Variant appearance in text: APOE: A80C
PubMed Link: 32438758
Variant Present in the following documents:
  • Main text
View BVdb publication page