Variant #0000886906 (NC_000005.9:g.77311370C>T, NM_003664.3:c.2995G>A (AP3B1))

Chromosome 5
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.77311370C>T
DNA change (hg38) -
Published as AP3B1(NM_001271769.1):c.2848G>A (p.V950M), AP3B1(NM_003664.4):c.2995G>A (p.V999M)
ISCN -
DB-ID AP3B1_000047 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) 0.00414 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     
AP3B1 NM_003664.3 -?/. - c.2995G>A r.(?) p.(Val999Met)


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