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DMD c.7542+13951G>C
Variant ID: X-31778126-C-G
NM_004006.2(
DMD
):c.7542+13951G>C
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:
Breakpoint junction features of seven DMD deletion mutations.
Human Genome Variation
Keegan, Niall P NP; Wilton, Steve D SD; Fletcher, Sue S
Publication Date: 2019
Variant appearance in text: rs6527115
PubMed Link:
31645977
Variant Present in the following documents:
Main text
41439_2019_Article_70.pdf
View BVdb publication page