Variant #0000234460 (NC_000023.10:g.31139998C>T, NM_004006.2:c.*38G>A (DMD))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31139998C>T
DNA change (hg38) g.31121881C>T
Published as DMD(NM_004006.2):c.*38G>A (p.(=)), DMD(NM_004021.2):c.3684G>A (p.A1228=), DMD(NM_004021.3):c.3684G>A (p.A1228=)
ISCN -
DB-ID DMD_000440 See all 6 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) 0.00251 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2016-11-24 10:23:00 +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.*38G>A r.(=) p.(=)


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