Variant #0000234465 (NC_000023.10:g.32472777A>T, NC_000023.10(NM_004006.2):c.3603+2T>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.32472777A>T
DNA change (hg38) g.32454660A>T
Published as DMD(NM_004006.2):c.3603+2T>A (p.?)
ISCN -
DB-ID DMD_000152 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) 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 2016-11-24 10:23:00 +01:00 (CET)
Date last edited 2020-07-19 18:00:04 +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 ?/. 26i c.3603+2T>A r.spl? p.?


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