ST6GAL1 c.980-108G>A

Variant ID: 3-186793242-G-A

NM_173216.2(ST6GAL1):c.980-108G>A

This variant was identified in 6 publications

View GRCh38 version.




Publications:


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: ST6GAL1: 980-108G>A; rs2239612
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: ST6GAL1: 980-108G>A; rs2239612
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 2
  • CNR2-4-e1335-s003.xlsx, sheet 1
View BVdb publication page



Cumulative evidence for association between genetic polymorphisms and esophageal cancer susceptibility: A review with evidence from meta-analysis and genome-wide association studies.

Cancer Medicine
Tian, Jie J; Liu, Caiyang C; Liu, Guanchu G; Zuo, Chunjian C; Chen, Huanwen H
Publication Date: 2019-03

Variant appearance in text: rs2239612
PubMed Link: 30793520
Variant Present in the following documents:
  • Main text
View BVdb publication page



Integration of VDR genome wide binding and GWAS genetic variation data reveals co-occurrence of VDR and NF-κB binding that is linked to immune phenotypes.

Bmc Genomics
Singh, Prashant K PK; van den Berg, Patrick R PR; Long, Mark D MD; Vreugdenhil, Angie A; Grieshober, Laurie L; Ochs-Balcom, Heather M HM; Wang, Jianmin J; Delcambre, Sylvie S; Heikkinen, Sami S; Carlberg, Carsten C; Campbell, Moray J MJ; Sucheston-Campbell, Lara E LE
Publication Date: 2017-02-06

Variant appearance in text: rs2239612
PubMed Link: 28166722
Variant Present in the following documents:
  • Main text
  • 12864_2017_Article_3481.pdf
View BVdb publication page



DIRC3 and near NABP1 genetic polymorphisms are associated laryngeal squamous cell carcinoma patient survival.

Oncotarget
Shen, Zhen Z; Ren, Wanli W; Bai, Yanxia Y; Chen, Zhengshuai Z; Li, Jingjie J; Li, Bin B; Jin, Tianbo T; Cao, Peilong P; Shao, Yuan Y
Publication Date: 2016-11-29

Variant appearance in text: rs2239612
PubMed Link: 27793000
Variant Present in the following documents:
  • Main text
  • oncotarget-07-79596.pdf
View BVdb publication page



Genetic variants at 6p21, 10q23, 16q21 and 22q12 are associated with esophageal cancer risk in a Chinese Han population.

International Journal Of Clinical And Experimental Medicine
Jia, Xiaobin X; Liu, Peng P; Zhang, Mingxia M; Feng, Tian T; Tang, Hongtao H; Tang, Zhigang Z; Zhao, Huaqian H; Jin, Tianbo T
Publication Date: 2015

Variant appearance in text: rs2239612
PubMed Link: 26770579
Variant Present in the following documents:
  • Main text
View BVdb publication page