DNAH11 c.273G>T ;(p.G91=)

Variant ID: 7-21583136-G-T

NM_001277115.1(DNAH11):c.273G>T;(p.G91=)

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: DNAH11: Gly91Gly
PubMed Link: 35304488
Variant Present in the following documents:
  • 41525_2022_294_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page