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DMD c.10705A>T ;(p.K3569*)
Variant ID: X-31165484-T-A
NM_004006.2(
DMD
):c.10705A>T;(p.K3569*)
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:
Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
Bmc Medical Genetics
Zhang, Jingjing J; Ma, Dingyuan D; Liu, Gang G; Wang, Yuguo Y; Liu, An A; Li, Li L; Luo, Chunyu C; Hu, Ping P; Xu, Zhengfeng Z
Publication Date: 2019-11-14
Variant appearance in text: DMD: Lys3569*
PubMed Link:
31727011
Variant Present in the following documents:
Main text
12881_2019_Article_912.pdf
View BVdb publication page