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C15orf48 c.*41C>G
Variant ID: 15-45725255-C-G
NM_197955.2(
C15orf48
):c.*41C>G
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:
Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition.
Bmc Genomics
Gupta, Hemant H; Chandratre, Khyati K; Sinha, Siddharth S; Huang, Teng T; Wu, Xiaobing X; Cui, Jian J; Zhang, Michael Q MQ; Wang, San Ming SM
Publication Date: 2020-11-30
Variant appearance in text: rs56073218
PubMed Link:
33256598
Variant Present in the following documents:
12864_2020_7222_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page
Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
Rna Biology
Duan, Shiwei S; Mi, Shuangli S; Zhang, Wei W; Dolan, M Eileen ME
Publication Date: 2009
Variant appearance in text: rs56073218
PubMed Link:
19458495
Variant Present in the following documents:
Main text
View BVdb publication page