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.




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