PC c.2075C>G ;(p.A692G)

Variant ID: 11-66618659-G-C

NM_001040716.1(PC):c.2075C>G;(p.A692G)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Decoding Conformational Imprint of Convoluted Molecular Interactions Between Prenylflavonoids and Aggregated Amyloid-Beta42 Peptide Causing Alzheimer's Disease.

Frontiers In Chemistry
Srinivasan, E E; Chandrasekhar, G G; Chandrasekar, P P; Anbarasu, K K; Vickram, A S AS; Tayubi, Iftikhar Aslam IA; Rajasekaran, R R; Karunakaran, Rohini R
Publication Date: 2021

Variant appearance in text: PC: A692G
PubMed Link: 34988060
Variant Present in the following documents:
  • Main text
View BVdb publication page



Publication of nuclear magnetic resonance experimental data with semantic web technology and the application thereof to biomedical research of proteins.

Journal Of Biomedical Semantics
Yokochi, Masashi M; Kobayashi, Naohiro N; Ulrich, Eldon L EL; Kinjo, Akira R AR; Iwata, Takeshi T; Ioannidis, Yannis E YE; Livny, Miron M; Markley, John L JL; Nakamura, Haruki H; Kojima, Chojiro C; Fujiwara, Toshimichi T
Publication Date: 2016-05-05

Variant appearance in text: PC: A692G
PubMed Link: 27927232
Variant Present in the following documents:
  • 13326_2016_57_MOESM1_ESM.pdf
View BVdb publication page



Oligomeric Aβ-induced synaptic dysfunction in Alzheimer's disease.

Molecular Neurodegeneration
Tu, Shichun S; Okamoto, Shu-ichi S; Lipton, Stuart A SA; Xu, Huaxi H
Publication Date: 2014-11-14

Variant appearance in text: PC: A692G
PubMed Link: 25394486
Variant Present in the following documents:
  • 13024_2014_Article_556.pdf
View BVdb publication page