SRA1 c.152-161G>C

Variant ID: 5-139931930-C-G

NM_001035235.4(SRA1):c.152-161G>C

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Association between long-chain non-coding RNA SRA1 gene single-nucleotide polymorphism and polycystic ovary syndrome susceptibility.

Journal Of Assisted Reproduction And Genetics
Tan, Jifan J; Hao, XiuLan X; Zhao, TingTing T; Ying, JianLan J; Li, Tian T; Cheng, Li L
Publication Date: 2020-10

Variant appearance in text: rs801460
PubMed Link: 32783135
Variant Present in the following documents:
  • Main text
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: rs801460
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
  • Table_5.xlsx, sheet 1
View BVdb publication page



New Insights Into the Long Non-coding RNA SRA: Physiological Functions and Mechanisms of Action.

Frontiers In Medicine
Sheng, Liang L; Ye, Lan L; Zhang, Dong D; Cawthorn, William P WP; Xu, Bin B
Publication Date: 2018

Variant appearance in text: rs801460
PubMed Link: 30238005
Variant Present in the following documents:
  • Main text
  • fmed-05-00244.pdf
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: rs801460
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs801460
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Dysregulation of long non-coding RNA in breast cancer: an overview of mechanism and clinical implication.

Oncotarget
Wang, Ji J; Ye, Chenyang C; Xiong, Hanchu H; Shen, Yong Y; Lu, Yi Y; Zhou, Jichun J; Wang, Linbo L
Publication Date: 2017-01-17

Variant appearance in text: rs801460
PubMed Link: 27732939
Variant Present in the following documents:
  • Main text
  • oncotarget-08-5508.pdf
View BVdb publication page



Genetic variants in lncRNA SRA and risk of breast cancer.

Oncotarget
Yan, Rui R; Wang, Kaijuan K; Peng, Rui R; Wang, Shuaibing S; Cao, Jingjing J; Wang, Peng P; Song, Chunhua C
Publication Date: 2016-04-19

Variant appearance in text: rs801460
PubMed Link: 26967566
Variant Present in the following documents:
  • Main text
  • oncotarget-07-22486.pdf
View BVdb publication page