Variant #0001045587 (NC_000001.10:g.114454061C>T, NM_006594.3:c.-6574G>A (AP4B1))

Chromosome 1
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.114454061C>T
DNA change (hg38) -
Published as DCLRE1B(NM_022836.4):c.847C>T (p.R283C)
ISCN -
DB-ID DCLRE1B_000002 See all 2 reported entries
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) 0.00145 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-07-08 13:22:38 +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     
AP4B1 NM_006594.3 -?/. - c.-6574G>A r.(?) p.(=)
DCLRE1B NM_022836.3 -?/. - c.847C>T r.(?) p.(Arg283Cys)


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