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MRE11 c.1098+1269G>A
Variant ID: 11-94199710-C-T
NM_005591.3(
MRE11
):c.1098+1269G>A
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:
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: rs11020790
PubMed Link:
33256598
Variant Present in the following documents:
12864_2020_7222_MOESM2_ESM.xlsx, sheet 19
12864_2020_7222_MOESM2_ESM.xlsx, sheet 21
12864_2020_7222_MOESM2_ESM.xlsx, sheet 20
12864_2020_7222_MOESM2_ESM.xlsx, sheet 17
12864_2020_7222_MOESM2_ESM.xlsx, sheet 2
12864_2020_7222_MOESM2_ESM.xlsx, sheet 3
12864_2020_7222_MOESM2_ESM.xlsx, sheet 4
View BVdb publication page
rs12416605:C>T in MIR938 associates with gastric cancer through affecting the regulation of the CXCL12 chemokine gene.
Molecular Genetics & Genomic Medicine
Torruella-Loran, Ignasi I; Ramirez Viña, María Karla MK; Zapata-Contreras, Daniela D; Muñoz, Xavier X; Garcia-Ramallo, Eva E; Bonet, Catalina C; Gonzalez, Carlos A CA; Sala, Núria N; Espinosa-Parrilla, Yolanda Y; ,
Publication Date: 2019-08
Variant appearance in text: rs11020790
PubMed Link:
31273931
Variant Present in the following documents:
Main text
MGG3-7-e832.pdf
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: rs11020790
PubMed Link:
19458495
Variant Present in the following documents:
Main text
View BVdb publication page