DMD c.9649+4A>T

Variant ID: X-31224695-T-A

NM_004006.2(DMD):c.9649+4A>T

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:

A novel DMD intronic alteration: a potentially disease-causing variant of an intermediate muscular dystrophy phenotype.

Acta Myologica : Myopathies And Cardiomyopathies : Official Journal Of The Mediterranean Society Of Myology
Santin, Ricardo R; Vieira, Igor Araujo IA; Nunes, Jean Costa JC; Benevides, Maria Luiza ML; Quadros, Fernanda F; Brusius-Facchin, Ana Carolina AC; Macedo, Gabriel G; Bertoni, Ana Paula Santin APS
Publication Date: 2021-06

Variant appearance in text: DMD: 9649+4A>T
PubMed Link: 34355126
Variant Present in the following documents:
  • Main text
View BVdb publication page