DMD c.6290G>T ;(p.G2097V)

Variant ID: X-32305646-C-A

NM_004006.2(DMD):c.6290G>T;(p.G2097V)

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:

[Application of next-generation sequencing in the molecular diagnosis of Duchenne muscular dystrophy].

Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal Of Contemporary Pediatrics
Tian, Pei-Chao PC; Wang, Yue Y; Shi, Dan-Dan DD; Chen, Zheng Z; Luo, Qiang Q; Wang, Huai-Li HL
Publication Date: 2019-03

Variant appearance in text: DMD: 6290G>T; Gly2097Val
PubMed Link: 30907348
Variant Present in the following documents:
  • Main text
View BVdb publication page