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DMD c.4859A>G ;(p.E1620G)
Variant ID: X-32383303-T-C
NM_004006.2(
DMD
):c.4859A>G;(p.E1620G)
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:
Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure.
Esc Heart Failure
Saito, Tsunenori T; Sato, Naoko Saito NS; Mozawa, Kosuke K; Adachi, Akiko A; Sasaki, Yoshihiro Y; Nakamura, Kotoka K; Oka, Eiichiro E; Otsuka, Toshiaki T; Kodani, Eitaro E; Asai, Kuniya K; Mizuno, Kyoichi K; Shimizu, Wataru W; Gottlieb, Roberta A RA
Publication Date: 2021-09-06
Variant appearance in text: DMD: 4859A>G; E1620G
PubMed Link:
34486814
Variant Present in the following documents:
Main text
EHF2-8-5178.pdf
View BVdb publication page
Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure.
Esc Heart Failure
Saito, Tsunenori T; Sato, Naoko Saito NS; Mozawa, Kosuke K; Adachi, Akiko A; Sasaki, Yoshihiro Y; Nakamura, Kotoka K; Oka, Eiichiro E; Otsuka, Toshiaki T; Kodani, Eitaro E; Asai, Kuniya K; Mizuno, Kyoichi K; Shimizu, Wataru W; Gottlieb, Roberta A RA
Publication Date: 2021-12
Variant appearance in text: DMD: 4859A>G; E1620G
PubMed Link:
34486814
Variant Present in the following documents:
Main text
EHF2-8-5178.pdf
View BVdb publication page