SLC35F3 c.385C>G ;(p.R129G)

Variant ID: 1-234367264-C-G

NM_173508.2(SLC35F3):c.385C>G;(p.R129G)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Integrative proteogenomic characterization of early esophageal cancer.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Zhang, Qiao Q; Liu, Hui H; Xu, Fujiang F; Guo, Chunmei C; Qin, Zhaoyu Z; Wang, Haixing H; Feng, Jinwen J; Liu, Yang Y; Chen, Weijie W; Zhang, Xue X; Bai, Lin L; Tian, Sha S; Tan, Subei S; Xu, Chen C; Song, Qi Q; Liu, Yalan Y; Zhong, Yunshi Y; Chen, Tianyin T; Zhou, Pinghong P; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-25

Variant appearance in text: SLC35F3: R129G; rs34032258
PubMed Link: 36966136
Variant Present in the following documents:
  • 41467_2023_37440_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



Effects of Interaction between SLC35F3 and Carbohydrate Intake on the Incidence of Metabolic Syndrome in Korean Middle-Aged Adults.

Nutrients
Park, Haeun H; Shin, Dayeon D
Publication Date: 2023-01-16

Variant appearance in text: rs34032258
PubMed Link: 36678339
Variant Present in the following documents:
  • Main text
  • nutrients-15-00469.pdf
View BVdb publication page



Genetic Variations in Thiamin Transferase SLC35F3 and the Risk of Hypertension in Koreans.

Clinical Nutrition Research
Seo, Ja-Young JY; Choi, Jeong-Hwa JH
Publication Date: 2021-04

Variant appearance in text: rs34032258
PubMed Link: 33987140
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of a SNP in SLC35F3 Gene with the Risk of Hypertension in a Chinese Han Population.

Frontiers In Genetics
Zang, Xiao-Li XL; Han, Wei-Qing WQ; Yang, Feng-Ping FP; Ji, Kai-Da KD; Wang, Ji-Guang JG; Gao, Ping-Jin PJ; He, Guang G; Wu, Sheng-Nan SN
Publication Date: 2016

Variant appearance in text: rs34032258
PubMed Link: 27379158
Variant Present in the following documents:
  • Main text
  • fgene-07-00108.pdf
View BVdb publication page



Identification of a novel SBF2 frameshift mutation in charcot-marie-tooth disease type 4B2 using whole-exome sequencing.

Genomics, Proteomics & Bioinformatics
Chen, Meiyan M; Wu, Jing J; Liang, Ning N; Tang, Lihui L; Chen, Yanhua Y; Chen, Huishuang H; Wei, Wei W; Wei, Tianying T; Huang, Hui H; Yi, Xin X; Qi, Ming M
Publication Date: 2014-10

Variant appearance in text: SLC35F3: 385C>G; R129G
PubMed Link: 25462154
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page