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TPST2 c.-160-10544G>A
Variant ID: 22-26951185-C-T
NM_003595.5(
TPST2
):c.-160-10544G>A
This variant was identified in 7 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Novel Risk Associations between microRNA Polymorphisms and Gastric Cancer in a Chilean Population.
International Journal Of Molecular Sciences
Landeros, Natalia N; Corvalan, Alejandro H AH; Musleh, Maher M; Quiñones, Luis A LA; Varela, Nelson M NM; Gonzalez-Hormazabal, Patricio P
Publication Date: 2021-12-31
Variant appearance in text: rs4822739
PubMed Link:
35008894
Variant Present in the following documents:
Main text
ijms-23-00467.pdf
View BVdb publication page
Novel Risk Associations between microRNA Polymorphisms and Gastric Cancer in a Chilean Population.
International Journal Of Molecular Sciences
Landeros, Natalia N; Corvalan, Alejandro H AH; Musleh, Maher M; Quiñones, Luis A LA; Varela, Nelson M NM; Gonzalez-Hormazabal, Patricio P
Publication Date: 2021-12-31
Variant appearance in text: rs4822739
PubMed Link:
35008894
Variant Present in the following documents:
Main text
ijms-23-00467.pdf
View BVdb publication page
Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.
Frontiers In Genetics
Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F
Publication Date: 2021
Variant appearance in text: rs4822739
PubMed Link:
34054912
Variant Present in the following documents:
Table_2.xlsx, sheet 1
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: rs4822739
PubMed Link:
31273931
Variant Present in the following documents:
Main text
MGG3-7-e832.pdf
View BVdb publication page
Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.
Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018
Variant appearance in text: rs4822739
PubMed Link:
30319441
Variant Present in the following documents:
Table_6.xlsx, sheet 1
View BVdb publication page
Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.
Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017
Variant appearance in text: rs4822739
PubMed Link:
28690861
Variant Present in the following documents:
hgv201727-s1.xls, sheet 1
View BVdb publication page
Polymorphism rs4919510:C>G in mature sequence of human microRNA-608 contributes to the risk of HER2-positive breast cancer but not other subtypes.
Plos One
Huang, A-Ji AJ; Yu, Ke-Da KD; Li, Jing J; Fan, Lei L; Shao, Zhi-Ming ZM
Publication Date: 2012
Variant appearance in text: rs4822739
PubMed Link:
22586447
Variant Present in the following documents:
Main text
pone.0035252.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: rs4822739
PubMed Link:
19458495
Variant Present in the following documents:
Main text
View BVdb publication page