PC c.216G>C ;(p.T72=)

Variant ID: 11-66639263-C-G

NM_001040716.1(PC):c.216G>C;(p.T72=)

This variant was identified in 3 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: PC: T72T
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
View BVdb publication page



Vector trace cells in the subiculum of the hippocampal formation.

Nature Neuroscience
Poulter, Steven S; Lee, Sang Ah SA; Dachtler, James J; Wills, Thomas J TJ; Lever, Colin C
Publication Date: 2021-02

Variant appearance in text: PC: t72=
PubMed Link: 33349710
Variant Present in the following documents:
  • Main text
  • EMS114905.pdf
View BVdb publication page



Safety of research into severe and treatment-resistant mood disorders: analysis of outcome data from 12 years of clinical trials at the US National Institute of Mental Health.

The Lancet. Psychiatry
Nugent, Allison C AC; Iadarola, Nicolas D ND; Miller, Frank G FG; Luckenbaugh, David A DA; Zarate, Carlos A CA
Publication Date: 2016-05

Variant appearance in text: PCB: t72=
PubMed Link: 26971192
Variant Present in the following documents:
  • Main text
View BVdb publication page