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DMD c.10751A>G ;(p.K3584R)
Variant ID: X-31165438-T-C
NM_004006.2(
DMD
):c.10751A>G;(p.K3584R)
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:
The lncRNA H19 alleviates muscular dystrophy by stabilizing dystrophin.
Nature Cell Biology
Zhang, Yaohua Y; Li, Yajuan Y; Hu, Qingsong Q; Xi, Yutao Y; Xing, Zhen Z; Zhang, Zhao Z; Huang, Lisa L; Wu, Jianbo J; Liang, Ke K; Nguyen, Tina K TK; Egranov, Sergey D SD; Sun, Chengcao C; Zhao, Zilong Z; Hawke, David H DH; Li, Jin J; Sun, Deqiang D; Kim, Jean J JJ; Zhang, Ping P; Cheng, Jie J; Farida, Abid A; Hung, Mien-Chie MC; Han, Leng L; Darabi, Radbod R; Lin, Chunru C; Yang, Liuqing L
Publication Date: 2020-11
Variant appearance in text: DMD: 10751A>G; K3584R
PubMed Link:
33106653
Variant Present in the following documents:
nihms-1630179.pdf
View BVdb publication page