DNAH11 c.5132A>G ;(p.Q1711R)

Variant ID: 7-21698453-A-G

NM_001277115.1(DNAH11):c.5132A>G;(p.Q1711R)

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:

A Study on the Genetics of Primary Ciliary Dyskinesia.

Journal Of Clinical Medicine
Alsamri, Mohammed T MT; Alabdouli, Amnah A; Iram, Durdana D; Alkalbani, Alia M AM; Almarzooqi, Ayesha S AS; Souid, Abdul-Kader AK; Vijayan, Ranjit R
Publication Date: 2021-10-30

Variant appearance in text: DNAH11: 5132A>G; Q1711R; rs189432084
PubMed Link: 34768622
Variant Present in the following documents:
  • Main text
  • jcm-10-05102.pdf
View BVdb publication page