Variant #0001038535 (NC_000011.9:g.61067666C>T, NM_001923.4:c.3365G>A (DDB1))

Chromosome 11
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.61067666C>T
DNA change (hg38) -
Published as DDB1(NM_001923.5):c.3365G>A (p.(Arg1122Gln))
ISCN -
DB-ID DAK_000016
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 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDB1 NM_001923.4 ?/. - c.3365G>A r.(?) p.(Arg1122Gln)
DAK NM_015533.3 ?/. - c.-33245C>T r.(?) p.(=)
VWCE NM_152718.2 ?/. - c.-5157G>A r.(?) p.(=)


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