Variant #0001053902 (NC_000011.9:g.61110810G>A, NM_001923.4:c.-10370C>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.61110810G>A
DNA change (hg38) -
Published as TKFC(NM_015533.4):c.866-4G>A
ISCN -
DB-ID CYBASC3_000015
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 2025-11-01 13:22:20 +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.-10370C>T r.(?) p.(=)
DAK NM_015533.3 -?/. - c.866-4G>A r.spl? p.?
CYBASC3 NM_153611.4 -?/. - c.*7061C>T r.(=) p.(=)


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