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DNAH11 c.11267G>A ;(p.R3756H)
Variant ID: 7-21901535-G-A
NM_001277115.1(
DNAH11
):c.11267G>A;(p.R3756H)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A prognostic risk model for glioma patients by systematic evaluation of genomic variations.
Iscience
Zhang, Baifeng B; Wan, Weiqing W; Li, Zibo Z; Gao, Zhixian Z; Ji, Nan N; Xie, Jian J; Wang, Junmei J; Wang, Bin B; Lai-Wan Kwong, Dora D; Guan, Xinyuan X; Gao, Shengjie S; Zhao, Yuanli Y; Lu, Youyong Y; Zhang, Liwei L; Rodland, Karin D KD; Tsang, Shirley X SX
Publication Date: 2022-12-22
Variant appearance in text: DNAH11: R3756H
PubMed Link:
36536675
Variant Present in the following documents:
mmc3.xls, sheet 1
View BVdb publication page
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: 11267G>A; rs554657293
PubMed Link:
34768622
Variant Present in the following documents:
Main text
jcm-10-05102.pdf
View BVdb publication page