Variant #0000847835 (NC_000023.10:g.32662432T>C, NC_000023.10(NM_004006.2):c.1150-2A>G (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.32662432T>C
DNA change (hg38) g.32644315T>C
Published as -
ISCN -
DB-ID DMD_003919 See all 8 reported entries
Variant remarks expression in 293T cells in vitro mini-gene splicing assay
Reference PubMed: Zhang 2022
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 2022-05-06 09:13:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMD NM_004006.2 +/. 10i c.1150-2A>G r.(1150_1331del) p.(Gly384Phefs*3)


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