Variant #0000260124 (NC_000015.9:g.51289980G>A, NM_001252127.1:c.2579G>A (AP4E1))

Chromosome 15
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.51289980G>A
DNA change (hg38) g.50997783G>A
Published as AP4E1(NM_001252127.2):c.2579G>A (p.W860*)
ISCN -
DB-ID AP4E1_000030
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-06 14:58:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP4E1 NM_001252127.1 +/. - c.2579G>A r.(?) p.(Trp860Ter)


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