DMD c.10127T>C ;(p.L3376P)

Variant ID: X-31196882-A-G

NM_004006.2(DMD):c.10127T>C;(p.L3376P)

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:

Genotype-Phenotype Correlations in Duchenne and Becker Muscular Dystrophy Patients from the Canadian Neuromuscular Disease Registry.

Journal Of Personalized Medicine
Lim, Kenji Rowel Q KRQ; Nguyen, Quynh Q; Yokota, Toshifumi T
Publication Date: 2020-11-23

Variant appearance in text: DMD: 10127T>C
PubMed Link: 33238405
Variant Present in the following documents:
  • Main text
  • jpm-10-00241.pdf
View BVdb publication page