Variant #0000655414 (NC_000005.9:g.77473154A>T, NC_000005.9(NM_003664.3):c.1040+9T>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.77473154A>T
DNA change (hg38) g.78177330A>T
Published as AP3B1(NM_001271769.1):c.893+9T>A, AP3B1(NM_001271769.2):c.893+9T>A, AP3B1(NM_003664.4):c.1040+9T>A
ISCN -
DB-ID AP3B1_000027 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) 0.00057 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP3B1 NM_003664.3 -?/. - c.1040+9T>A r.(=) p.(=)


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