MRE11 c.1563+1055C>T

Variant ID: 11-94188387-G-A

NM_005591.3(MRE11):c.1563+1055C>T

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: rs569143
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



Homologous Recombination Deficiency: Cancer Predispositions and Treatment Implications.

The Oncologist
Toh, MingRen M; Ngeow, Joanne J
Publication Date: 2021-09

Variant appearance in text: rs569143
PubMed Link: 34021944
Variant Present in the following documents:
  • Main text
View BVdb publication page