Variant #0001038536 (NC_000011.9:g.61070049C>A, NC_000011.9(NM_001923.4):c.3112+5G>T (DDB1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61070049C>A
DNA change (hg38) -
Published as DDB1(NM_001923.5):c.3112+5G>T
ISCN -
DB-ID DAK_000017
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) 0.00061 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 2025-05-05 21:14:00 +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     
DDB1 NM_001923.4 -?/. - c.3112+5G>T r.spl? p.?
DAK NM_015533.3 -?/. - c.-30862C>A r.(?) p.(=)


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