Variant #0000999184 (NC_000011.9:g.61109957G>A, NM_001923.4:c.-9517C>T (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.61109957G>A
DNA change (hg38) -
Published as DAK(NM_015533.3):c.680G>A (p.(Arg227His))
ISCN -
DB-ID CYBASC3_000011
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) 4.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
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.-9517C>T r.(?) p.(=)
DAK NM_015533.3 ?/. - c.680G>A r.(?) p.(Arg227His)
CYBASC3 NM_153611.4 ?/. - c.*7914C>T r.(=) p.(=)


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