APP c.111C>G ;(p.F37L)

Variant ID: 21-27484410-G-C

NM_000484.3(APP):c.111C>G;(p.F37L)

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:

CHIP as a therapeutic target for neurological diseases.

Cell Death & Disease
Zhang, Shuo S; Hu, Zheng-Wei ZW; Mao, Cheng-Yuan CY; Shi, Chang-He CH; Xu, Yu-Ming YM
Publication Date: 2020-09-09

Variant appearance in text: APP: 111C>G; Phe37Leu
PubMed Link: 32908122
Variant Present in the following documents:
  • Main text
View BVdb publication page