DMD c.6923_6933del ;(p.A2308Efs*6)

Variant ID: X-31893469-TCTCAGGTAAAG-T

NM_004006.2(DMD):c.6923_6933del;(p.A2308Efs*6)

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Corrigendum: Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.

Journal Of Human Genetics
Okubo, Mariko M; Minami, Narihiro N; Goto, Kanako K; Goto, Yuichi Y; Noguchi, Satoru S; Mitsuhashi, Satomi S; Nishino, Ichizo I
Publication Date: 2017-10

Variant appearance in text: DMD: 6923_6933del; Ala2308Glufs*6
PubMed Link: 28943641
Variant Present in the following documents:
  • 10038_2017_Article_BFjhg201754.pdf
View BVdb publication page


Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.

Journal Of Human Genetics
Okubo, Mariko M; Minami, Narihiro N; Goto, Kanako K; Goto, Yuichi Y; Noguchi, Satoru S; Mitsuhashi, Satomi S; Nishino, Ichizo I
Publication Date: 2016-06

Variant appearance in text: DMD: 6923_6933del; Ala2308Glufs*6
PubMed Link: 26911353
Variant Present in the following documents:
  • Main text
  • jhg20167a.pdf
View BVdb publication page