DMD c.10368del ;(p.N3456Kfs*10)

Variant ID: X-31190491-CA-C

NM_004006.2(DMD):c.10368del;(p.N3456Kfs*10)

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:

Quantitative Muscle MRI and Clinical Findings in Women With Pathogenic Dystrophin Gene Variants.

Frontiers In Neurology
Fornander, Freja F; Solheim, Tuva Åsatun TÅ; Eisum, Anne-Sofie Vibæk AV; Poulsen, Nanna Scharff NS; Andersen, Annarita Ghosh AG; Dahlqvist, Julia Rebecka JR; Dunø, Morten M; Vissing, John J
Publication Date: 2021

Variant appearance in text: DMD: 10368delT
PubMed Link: 34539555
Variant Present in the following documents:
  • Main text
  • fneur-12-707837.pdf
View BVdb publication page