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DNAH11 c.3853-24C>T
Variant ID: 7-21654708-C-T
NM_001277115.1(
DNAH11
):c.3853-24C>T
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:
Case Report: The novel hemizygous mutation in the SSR4 gene caused congenital disorder of glycosylation type iy: A case study and literature review.
Frontiers In Genetics
Wang, Jun J; Gou, Xingqing X; Wang, Xiyi X; Zhang, Jing J; Zhao, Nan N; Wang, Xiaohong X
Publication Date: 2022
Variant appearance in text: DNAH11: 3853-24C>T; rs182638542
PubMed Link:
36386804
Variant Present in the following documents:
Table1.xls, sheet 1
View BVdb publication page