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DMD c.7872+6321_7872+6379del
Variant ID: X-31691113-CTAAGTCGGGCCAAATAAAGGCAAGGCCATGTATATAGGTTTATTCCAGGGAGCTGCAAG-C
NM_004006.2(
DMD
):c.7872+6321_7872+6379del
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:
Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies.
Human Mutation
Ling, Chao C; Dai, Yi Y; Fang, Li L; Yao, Fengxia F; Liu, Zhe Z; Qiu, Zhengqing Z; Cui, Liying L; Xia, Fan F; Zhao, Chen C; Zhang, Shuyang S; Wang, Kai K; Zhang, Xue X
Publication Date: 2020-03
Variant appearance in text: DMD: 7309+15311_7872+6382del
PubMed Link:
31705731
Variant Present in the following documents:
Main text
HUMU-41-668.pdf
View BVdb publication page