Variant #0000257901 (NC_000005.9:g.77563373del, NM_003664.3:c.177del (AP3B1))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.77563373del
DNA change (hg38) g.78267549del
Published as AP3B1(NM_001271769.1):c.30delA (p.(Lys10AsnfsTer5)), AP3B1(NM_001271769.2):c.30delA (p.K10Nfs*5), AP3B1(NM_003664.5):c.177delA (p.K59Nfs*5)
ISCN -
DB-ID AP3B1_000034 See all 3 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP3B1 NM_003664.3 +/. - c.177del r.(?) p.(Lys59AsnfsTer5)


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