Bibliome.ai browser hg19
Search
About
Stats
FAQ
DMD c.10333G>A ;(p.A3445T)
Variant ID: X-31190526-C-T
NM_004006.2(
DMD
):c.10333G>A;(p.A3445T)
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:
Clinical utility in infants with suspected monogenic conditions through next-generation sequencing.
Molecular Genetics & Genomic Medicine
Hong, Sha S; Wang, Li L; Zhao, Dongying D; Zhang, Yonghong Y; Chen, Yan Y; Tan, Jintong J; Liang, Lili L; Zhu, Tianwen T
Publication Date: 2019-06
Variant appearance in text: DMD: 10333G>A
PubMed Link:
30968598
Variant Present in the following documents:
Main text
MGG3-7-e684.pdf
View BVdb publication page