Variant #0000333584 (NC_000023.10:g.31140007_31140019del, NM_004006.2:c.*23_*35del (DMD))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31140007_31140019del
DNA change (hg38) g.31121890_31121902del
Published as DMD(NM_000109.3):c.*23_*35del (p.(=)), DMD(NM_004006.3):c.*23_*35delTGATTTGGGCAGA, DMD(NM_004021.2):c.3669_3681delTGATTTGGGCAGA (p.D1223Efs*6)
ISCN -
DB-ID DMD_000960 See all 7 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMD NM_004006.2 -/. 79 c.*23_*35del r.(=) p.(=)


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