USH2A c.10740+7G>A

Variant ID: 1-215955377-C-T

NM_206933.2(USH2A):c.10740+7G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel.

Human Genomics
Ma, Jing J; Ma, Xiuli X; Lin, Ken K; Huang, Rui R; Bi, Xianyun X; Ming, Cheng C; Li, Li L; Li, Xia X; Li, Guo G; Zhao, Liping L; Yang, Tao T; Gao, Yingqin Y; Zhang, Tiesong T
Publication Date: 2023-01-04

Variant appearance in text: USH2A: 10740+7G>A
PubMed Link: 36597107
Variant Present in the following documents:
  • 40246_2022_449_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children.

Neural Plasticity
Xie, Le L; Qiu, Yue Y; Jin, Yuan Y; Xu, Kai K; Bai, Xue X; Liu, Xiao-Zhou XZ; Wang, Xiao-Hui XH; Chen, Sen S; Sun, Yu Y
Publication Date: 2021

Variant appearance in text: USH2A: 10740+7G>A
PubMed Link: 34335733
Variant Present in the following documents:
  • Main text
  • NP2021-6151973.pdf
View BVdb publication page