TMEM61 c.15+1300G>C

Variant ID: 1-55448053-G-C

NM_182532.1(TMEM61):c.15+1300G>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: rs2433675
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.

American Journal Of Human Genetics
Oliveira, Sofia A SA; Li, Yi-Ju YJ; Noureddine, Maher A MA; Zuchner, Stephan S; Qin, Xuejun X; Pericak-Vance, Margaret A MA; Vance, Jeffery M JM
Publication Date: 2005-08

Variant appearance in text: rs2433675
PubMed Link: 15986317
Variant Present in the following documents:
  • Main text
View BVdb publication page