Variant #0001038537 (NC_000011.9:g.61070945G>C, NC_000011.9(NM_001923.4):c.2833-318C>G (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.61070945G>C
DNA change (hg38) -
Published as DDB1(NM_001923.5):c.2833-318C>G
ISCN -
DB-ID DAK_000018
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDB1 NM_001923.4 -?/. - c.2833-318C>G r.(=) p.(=)
DAK NM_015533.3 -?/. - c.-29966G>C r.(?) p.(=)


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