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DMD c.2662_2664delinsAAC ;(p.E888N)
Variant ID: X-32503175-TTC-GTT
NM_004006.2(
DMD
):c.2662_2664delinsAAC;(p.E888N)
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:
Targeted sequencing of the DMD locus: A comprehensive diagnostic tool for all mutations.
The Indian Journal Of Medical Research
Aravind, Sankaramoorthy S; Ashley, Berty B; Mannan, Ashraf A; Ganapathy, Aparna A; Ramesh, Keerthi K; Ramachandran, Aparna A; Nongthomba, Upendra U; Shastry, Arun A
Publication Date: 2019-09
Variant appearance in text: DMD: Glu888Asn
PubMed Link:
31719299
Variant Present in the following documents:
Main text
IJMR-150-282.pdf
View BVdb publication page