Variant #0001053899 (NC_000011.9:g.61099042A>C, NM_001923.4:c.183T>G (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.61099042A>C
DNA change (hg38) -
Published as DDB1(NM_001923.5):c.183T>G (p.(Ile61Met))
ISCN -
DB-ID CYBASC3_000012
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 2025-11-01 13:22:20 +01:00 (CET)
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.183T>G r.(?) p.(Ile61Met)
DAK NM_015533.3 ?/. - c.-1869A>C r.(?) p.(=)
CYBASC3 NM_153611.4 ?/. - c.*18829T>G r.(=) p.(=)


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