DMD c.9G>T ;(p.W3C)

Variant ID: X-33229421-C-A

NM_004006.2(DMD):c.9G>T;(p.W3C)

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:

DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History Study.

Neurology
Bello, Luca L; Morgenroth, Lauren P LP; Gordish-Dressman, Heather H; Hoffman, Eric P EP; McDonald, Craig M CM; Cirak, Sebahattin S; ,
Publication Date: 2016-07-26

Variant appearance in text: DMD: 9G>T
PubMed Link: 27343068
Variant Present in the following documents:
  • Main text
View BVdb publication page