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CAND1 c.-290C>T
Variant ID: 12-67663208-C-T
NM_018448.3(
CAND1
):c.-290C>T
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: rs17103637
PubMed Link:
30202817
Variant Present in the following documents:
HEP4-2-1021-s001.xlsx, sheet 1
View BVdb publication page
Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.
Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10
Variant appearance in text: CAND1: -290C>T; rs17103637
PubMed Link:
29221171
Variant Present in the following documents:
oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page