USH2A c.9571-9A>G

Variant ID: 1-215987255-T-C

NM_206933.2(USH2A):c.9571-9A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Pervasive occurrence of splice-site-creating mutations and their possible involvement in genetic disorders.

Npj Genomic Medicine
Sakaguchi, Narumi N; Suyama, Mikita M
Publication Date: 2022-03-18

Variant appearance in text: USH2A: 9571-9A>G; rs767149705
PubMed Link: 35304488
Variant Present in the following documents:
  • 41525_2022_294_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page