Variant #0000526049 (NC_000005.9:g.77335063G>A, NM_003664.3:c.2613C>T (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.77335063G>A
DNA change (hg38) g.78039239G>A
Published as AP3B1(NM_001271769.1):c.2466C>T (p.H822=), AP3B1(NM_001271769.2):c.2466C>T (p.H822=), AP3B1(NM_003664.4):c.2613C>T (p.H871=)
ISCN -
DB-ID AP3B1_000016 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) 0.00402 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 11:24:01 +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.2613C>T r.(?) p.(His871=)


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