Variant #0000850964 (NC_000005.9:g.77473181C>T, NM_003664.3:c.1022G>A (AP3B1))

Chromosome 5
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.77473181C>T
DNA change (hg38) -
Published as AP3B1(NM_001271769.1):c.875G>A (p.R292H), AP3B1(NM_001271769.2):c.875G>A (p.R292H), AP3B1(NM_003664.5):c.1022G>A (p.(Arg341His))
ISCN -
DB-ID AP3B1_000044 See all 4 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) 0.00022 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP3B1 NM_003664.3 ?/. - c.1022G>A r.(?) p.(Arg341His)


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