USH2A c.7068T>C ;(p.N2356=)

Variant ID: 1-216138711-A-G

NM_206933.2(USH2A):c.7068T>C;(p.N2356=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Novel biallelic USH2A variants in a patient with usher syndrome type IIA- a case report.

Bmc Ophthalmology
Young, Su Ling SL; Stanton, Chloe M CM; Livesey, Benjamin J BJ; Marsh, Joseph A JA; Cackett, Peter D PD
Publication Date: 2022-03-26

Variant appearance in text: rs200038092
PubMed Link: 35346118
Variant Present in the following documents:
  • 12886_2022_2353_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Whole exome sequencing reveals novel EYS mutations in Chinese patients with autosomal recessive retinitis pigmentosa.

Molecular Vision
Xiao, Xiaoqiang X; Cao, Yingjie Y; Chen, Shaowan S; Chen, Min M; Mai, Xiaoting X; Zheng, Yuqian Y; Zhuang, Xi X; Ng, Tsz Kin TK; Chen, Haoyu H
Publication Date: 2019

Variant appearance in text: rs200038092
PubMed Link: 30804660
Variant Present in the following documents:
  • mv-v25-35.pdf
View BVdb publication page