Variant #0000644131 (NC_000023.10:g.32716064G>A, NM_004006.2:c.883C>T (DMD))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32716064G>A
DNA change (hg38) g.32697947G>A
Published as -
ISCN -
DB-ID DMD_001638 See all 20 reported entries
Variant remarks exon skipping in mini-gene splicing assay 0.15
Reference PubMed: Okubo 2020
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-02-11 22:52:03 +01:00 (CET)
Date last edited 2020-07-14 21:43:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMD NM_004006.2 +/. 9 c.883C>T r.[883c>u,832_960del] p.[Arg295*,Ile278_Gln320del]


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