PC c.587C>G ;(p.A196G)

Variant ID: 11-66638569-G-C

NM_001040716.1(PC):c.587C>G;(p.A196G)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Brain-derived neurotrophic factor rs6265 (Val66Met) single nucleotide polymorphism as a master modifier of human pathophysiology.

Neural Regeneration Research
Nguyen, Van Thuan VT; Hill, Braxton B; Sims, Naiya N; Heck, Aaron A; Negron, Marcus M; Lusk, Claire C; Galindo, Cristi L CL
Publication Date: 2023-01

Variant appearance in text: PC: A196G
PubMed Link: 35799516
Variant Present in the following documents:
  • NRR-18-102_Suppl1.pdf
View BVdb publication page



BDNF Polymorphism: A Review of Its Diagnostic and Clinical Relevance in Neurodegenerative Disorders.

Aging And Disease
Shen, Ting T; You, Yuyi Y; Joseph, Chitra C; Mirzaei, Mehdi M; Klistorner, Alexander A; Graham, Stuart L SL; Gupta, Vivek V
Publication Date: 2018-06

Variant appearance in text: PC: A196G
PubMed Link: 29896439
Variant Present in the following documents:
  • ad-9-3-523.pdf
View BVdb publication page



Chemical shift tensor - the heart of NMR: Insights into biological aspects of proteins.

Progress In Nuclear Magnetic Resonance Spectroscopy
Saitô, Hazime H; Ando, Isao I; Ramamoorthy, Ayyalusamy A
Publication Date: 2010-08

Variant appearance in text: PC: A196G
PubMed Link: 20633363
Variant Present in the following documents:
  • Main text
View BVdb publication page