APP c.67_68delinsCC ;(p.D23P)

Variant ID: 21-27484453-TC-GG

NM_000484.3(APP):c.67_68delinsCC;(p.D23P)

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:

Single Point Mutation from E22-to-K in Aβ Initiates Early-Onset Alzheimer's Disease by Binding with Catalase.

Oxidative Medicine And Cellular Longevity
Jiang, Wenjing W; YanYu, ; Yao, Dandan D; Fei, Xuechao X; Ai, Li L; Di, Yalan Y; Zhang, Jingnan J; Yue, Xiangpei X; Zhao, Shengjie S; He, Rongqiao R; Lyu, Jihui J; Tong, Zhiqian Z
Publication Date: 2020

Variant appearance in text: APP: D23P
PubMed Link: 33425208
Variant Present in the following documents:
  • OMCL2020-4981204.pdf
View BVdb publication page