Variant #0000990126 (NC_000001.10:g.114443898C>T, NM_006594.3:c.577G>A (AP4B1))

Chromosome 1
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.114443898C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID AP4B1_000054 See all 2 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) 7.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L15 NM_001010922.2 +/. - c.-13901G>A r.(?) p.(=)
AP4B1 NM_006594.3 +/. - c.577G>A r.(?) p.(Val193Ile)
PTPN22 NM_015967.5 +/. - c.-29653G>A r.(?) p.(=)
DCLRE1B NM_022836.3 +/. - c.-4311C>T r.(?) p.(=)


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