Bibliome.ai browser hg19
Search
About
Stats
FAQ
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