DMD c.7542+9297G>A

Variant ID: X-31782780-C-T

NM_004006.2(DMD):c.7542+9297G>A

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:

Exome sequencing identifies novel and known mutations in families with intellectual disability.

Bmc Medical Genomics
Rasheed, Memoona M; Khan, Valeed V; Harripaul, Ricardo R; Siddiqui, Maimoona M; Malik, Madiha Amin MA; Ullah, Zahid Z; Zahid, Muhammad M; Vincent, John B JB; Ansar, Muhammad M
Publication Date: 2021-08-27

Variant appearance in text: rs16998223
PubMed Link: 34452636
Variant Present in the following documents:
  • Main text
  • 12920_2021_Article_1066.pdf
View BVdb publication page