DNAH11 c.7085G>A ;(p.R2362K)

Variant ID: 7-21757494-G-A

NM_001277115.1(DNAH11):c.7085G>A;(p.R2362K)

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:

Whole-exome Sequencing Helps the Diagnosis and Treatment in Children with Neurodevelopmental Delay Accompanied Unexplained Dyspnea.

Scientific Reports
Tong, Wenjia W; Wang, Yajian Y; Lu, Yun Y; Ye, Tongsheng T; Song, Conglei C; Xu, Yuanyuan Y; Li, Min M; Ding, Jie J; Duan, Yuanyuan Y; Zhang, Le L; Gu, Weiyue W; Zhao, Xiaoling X; Yang, Xiu-An XA; Jin, Danqun D
Publication Date: 2018-03-26

Variant appearance in text: DNAH11: 7085G>A; R2362Q
PubMed Link: 29581464
Variant Present in the following documents:
  • 41598_2018_23503_MOESM1_ESM.xls, sheet 17
View BVdb publication page