Bibliome.ai browser hg19
Search
About
Stats
FAQ
DNAH11 c.13273G>A ;(p.G4425S)
Variant ID: 7-21939708-G-A
NM_001277115.1(
DNAH11
):c.13273G>A;(p.G4425S)
This variant was identified in 3 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: 13273G>A; Gly4425Ser
PubMed Link:
34133440
Variant Present in the following documents:
Main text
pone.0252786.pdf
View BVdb publication page
A novel DNAH11 variant segregating in a sibship with heterotaxy and implications for genetic counseling.
Molecular Genetics & Genomic Medicine
Namavarian, Amirpouyan A; Eid, Anas A; Goh, Elaine Suk-Ying ES; Thakur, Varsha V
Publication Date: 2020-09
Variant appearance in text: DNAH11: 13273G>A; Gly4425Ser
PubMed Link:
32633470
Variant Present in the following documents:
Main text
MGG3-8-e1358.pdf
View BVdb publication page
DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome.
Scientific Reports
Liu, Sida S; Chen, Weicheng W; Zhan, Yongkun Y; Li, Shuolin S; Ma, Xiaojing X; Ma, Duan D; Sheng, Wei W; Huang, Guoying G
Publication Date: 2019-04-30
Variant appearance in text: DNAH11: G4425S
PubMed Link:
31040315
Variant Present in the following documents:
Main text
41598_2019_Article_43109.pdf
View BVdb publication page