Overview

Variant ID 28913
Entrez Gene ID 1756
Gene DMD (GeneCards)
Location hg19 X:32369774-32369774
hg38 X:32351657-32351657
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000023.10:g.32369774 T>A (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 155270560

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
CADD Raw score (version 1.3) 0.322711 (Deleterious)
FATHMM raw prediction score 0.1063 (Tolerated)
Deleterious probability by DeFine 0.6053 (Deleterious)
Entrez Gene ID 1756 (NCBI Gene)
Official Gene Symbol DMD (GeneCards)
Number of variants in DMD in this database 51 (view all the variants)
Full name dystrophin
Band Xp21.2-p21.1
Other IDs Vega: OTTHUMG00000021336
OMIM: 300377
HGNC: HGNC:2928
Ensembl: ENSG00000198947
Other names BMD, CMD3B, MRX85, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272
Summary This gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [provided by RefSeq, Dec 2016]

Individual #1

Individual ID 29217587.03 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID