Variant #0000234263 (NC_000023.10:g.31676096G>A, NC_000023.10(NM_004006.2):c.8027+11C>T (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.31676096G>A
DNA change (hg38) g.31657979G>A
Published as DMD(NM_004006.3):c.8027+11C>T, DMD(NM_004010.3):c.7658+11C>T
ISCN -
DB-ID DMD_001016 See all 31 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) 0.33362 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2017-11-28 14:29:49 +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 -/. 54i c.8027+11C>T r.(=) p.(=)


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