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DMD c.5524_5526delinsTGG ;(p.R1842W)
Variant ID: X-32364120-TCT-CCA
NM_004006.2(
DMD
):c.5524_5526delinsTGG;(p.R1842W)
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 and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent.
Frontiers In Neurology
Chakravorty, Samya S; Nallamilli, Babi Ramesh Reddy BRR; Khadilkar, Satish Vasant SV; Singla, Madhu Bala MB; Bhutada, Ashish A; Dastur, Rashna R; Gaitonde, Pradnya Satish PS; Rufibach, Laura E LE; Gloster, Logan L; Hegde, Madhuri M
Publication Date: 2020
Variant appearance in text: DMD: R1842W
PubMed Link:
33250842
Variant Present in the following documents:
Main text
fneur-11-559327.pdf
View BVdb publication page