Variant #0000882695 (NC_000001.10:g.114450804A>G, NM_006594.3:c.-3317T>C (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.114450804A>G
DNA change (hg38) -
Published as DCLRE1B(NM_022836.4):c.529A>G (p.I177V)
ISCN -
DB-ID AP4B1_000069
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
AP4B1 NM_006594.3 -?/. - c.-3317T>C r.(?) p.(=)
DCLRE1B NM_022836.3 -?/. - c.529A>G r.(?) p.(Ile177Val)


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