APP c.46_48delinsTGT ;(p.R16C)

Variant ID: 21-27542891-CCG-ACA

NM_000484.3(APP):c.46_48delinsTGT;(p.R16C)

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:

Astrocytic phagocytosis contributes to demyelination after focal cortical ischemia in mice.

Nature Communications
Wan, Ting T; Zhu, Wusheng W; Zhao, Ying Y; Zhang, Xiaohao X; Ye, Ruidong R; Zuo, Meng M; Xu, Pengfei P; Huang, Zhenqian Z; Zhang, Chunni C; Xie, Yi Y; Liu, Xinfeng X
Publication Date: 2022-03-03

Variant appearance in text: APP: R16C
PubMed Link: 35241660
Variant Present in the following documents:
  • 41467_2022_28777_MOESM3_ESM.pdf
View BVdb publication page