CP c.2571C>T ;(p.Y857=)

Variant ID: 3-148897433-G-A

NM_000096.3(CP):c.2571C>T;(p.Y857=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole-Exome Sequencing Study of Extreme Phenotypes of NAFLD.

Hepatology Communications
Kleinstein, Sarah E SE; Rein, Matthew M; Abdelmalek, Manal F MF; Guy, Cynthia D CD; Goldstein, David B DB; Mae Diehl, Anna A; Moylan, Cynthia A CA
Publication Date: 2018-09

Variant appearance in text: rs151304828
PubMed Link: 30202817
Variant Present in the following documents:
  • HEP4-2-1021-s001.xlsx, sheet 5
View BVdb publication page



Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders.

Parkinson'S Disease
Castiglioni, Emanuela E; Finazzi, Dario D; Goldwurm, Stefano S; Pezzoli, Gianni G; Forni, Gianluca G; Girelli, Domenico D; Maccarinelli, Federica F; Poli, Maura M; Ferrari, Maurizio M; Cremonesi, Laura L; Arosio, Paolo P
Publication Date: 2010-10-17

Variant appearance in text: CP: Y857Y
PubMed Link: 20981230
Variant Present in the following documents:
  • Main text
  • PD2011-827693.pdf
View BVdb publication page