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DNAH11 c.2832dup ;(p.Q945Sfs*10)
Variant ID: 7-21639563-G-GT
NM_001277115.1(
DNAH11
):c.2832dup;(p.Q945Sfs*10)
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:
DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease.
Plos One
Xia, Hong H; Huang, Xiangjun X; Deng, Sheng S; Xu, Hongbo H; Yang, Yan Y; Liu, Xin X; Yuan, Lamei L; Deng, Hao H
Publication Date: 2021
Variant appearance in text: DNAH11: 2832dup; Gln945Serfs
PubMed Link:
34133440
Variant Present in the following documents:
Main text
pone.0252786.pdf
View BVdb publication page
Somatic mutation of DNAH genes implicated higher chemotherapy response rate in gastric adenocarcinoma patients.
Journal Of Translational Medicine
Zhu, Chunchao C; Yang, Qin Q; Xu, Jia J; Zhao, Wenyi W; Zhang, Zizhen Z; Xu, Danhua D; Zhang, Yeqian Y; Zhao, Enhao E; Zhao, Gang G
Publication Date: 2019-04-03
Variant appearance in text: DNAH11: Q945Sfs*10
PubMed Link:
30944005
Variant Present in the following documents:
12967_2019_1867_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page