DMD c.1929G>A ;(p.W643*)

Variant ID: X-32583882-C-T

NM_004006.2(DMD):c.1929G>A;(p.W643*)

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:

Noninvasive prenatal diagnosis of duchenne muscular dystrophy in five Chinese families based on relative mutation dosage approach.

Bmc Medical Genomics
Zhao, Ganye G; Wang, Xiaofeng X; Liu, Lina L; Dai, Peng P; Kong, Xiangdong X
Publication Date: 2021-11-22

Variant appearance in text: DMD: 1929G>A; Trp643Ter
PubMed Link: 34802424
Variant Present in the following documents:
  • Main text
  • 12920_2021_Article_1128.pdf
View BVdb publication page