DLG2 c.520-65667G>C

Variant ID: 11-84028001-C-G

NM_001142699.1(DLG2):c.520-65667G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.

Bmc Medical Genetics
Zhou, Yingjie Y; Tariq, Muhammad M; He, Sijie S; Abdullah, Uzma U; Zhang, Jianguo J; Baig, Shahid Mahmood SM
Publication Date: 2020-07-18

Variant appearance in text: rs557645711
PubMed Link: 32682410
Variant Present in the following documents:
  • 12881_2020_1087_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page