Variant #0000257916 (NC_000019.9:g.2102183C>T, NM_003938.6:c.3451G>A (AP3D1))

Chromosome 19
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.2102183C>T
DNA change (hg38) g.2102184C>T
Published as AP3D1(NM_001261826.3):c.3637G>A (p.A1213T)
ISCN -
DB-ID AP3D1_000001
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) 8.0E-5 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IZUMO4 NM_001039846.1 ?/. - c.*2839C>T r.(=) p.(=)
AP3D1 NM_003938.6 ?/. - c.3451G>A r.(?) p.(Ala1151Thr)


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