Variant #0001065478 (NC_000011.9:g.61120344C>T, NM_001923.4:c.-19904G>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.61120344C>T
DNA change (hg38) -
Published as TKFC(NM_001351978.2):c.1588C>T (p.(Pro530Ser))
ISCN -
DB-ID chr11_008674
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 2026-01-20 18:57:21 +01:00 (CET)
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.-19904G>A r.(?) p.(=)
DAK NM_015533.3 ?/. - c.*6369C>T r.(=) p.(=)
TMEM138 NM_016464.4 ?/. - c.-9688C>T r.(?) p.(=)
CYBASC3 NM_153611.4 ?/. - c.548+113G>A r.(=) p.(=)


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