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