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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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