DNAH11 c.9631C>T ;(p.P3211S)

Variant ID: 7-21826275-C-T

NM_001277115.1(DNAH11):c.9631C>T;(p.P3211S)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Clinical characteristics and genetic spectrum of 26 individuals of Chinese origin with primary ciliary dyskinesia.

Orphanet Journal Of Rare Diseases
Zhao, Xinyue X; Bian, Chun C; Liu, Keqiang K; Xu, Wenshuai W; Liu, Yaping Y; Tian, Xinlun X; Bai, Jing J; Xu, Kai-Feng KF; Zhang, Xue X
Publication Date: 2021-07-01

Variant appearance in text: DNAH11: 9631C>T; P3211S
PubMed Link: 34210339
Variant Present in the following documents:
  • Main text
  • 13023_2021_Article_1840.pdf
  • 13023_2021_1840_MOESM2_ESM.xls, sheet 1
View BVdb publication page