Bibliome.ai browser hg19
Search
About
Stats
FAQ
DNAH11 c.13010G>A ;(p.S4337N)
Variant ID: 7-21934578-G-A
NM_001277115.1(
DNAH11
):c.13010G>A;(p.S4337N)
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: 13010G>A; S4337N; rs759646661
PubMed Link:
34768622
Variant Present in the following documents:
Main text
jcm-10-05102.pdf
View BVdb publication page