ST8SIA6 c.636-13T>C

Variant ID: 10-17365169-A-G

NM_001004470.1(ST8SIA6):c.636-13T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs12354751
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



Genetic dissection of yield traits in super hybrid rice Xieyou9308 using both unconditional and conditional genome-wide association mapping.

Scientific Reports
Zhang, Yingxin Y; Zhou, Liyuan L; Shen, Xihong X; Chen, Daibo D; Wu, Weixun W; Zhan, Xiaodeng X; Liu, Qunen Q; Zhu, Aike A; Lou, Xiangyang X; Xu, Haiming H; Cheng, Shihua S; Cao, Liyong L
Publication Date: 2017-04-11

Variant appearance in text: rs12354751
PubMed Link: 28400567
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_938.pdf
View BVdb publication page