Variant #0000604670 (NC_000001.10:g.114444403T>G, NM_006594.3:c.443A>C (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.114444403T>G
DNA change (hg38) g.113901781T>G
Published as AP4B1(NM_006594.5):c.443A>C (p.H148P)
ISCN -
DB-ID AP4B1_000044
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L15 NM_001010922.2 +/. - c.-14406A>C r.(?) p.(=)
AP4B1 NM_006594.3 +/. - c.443A>C r.(?) p.(His148Pro)
PTPN22 NM_015967.5 +/. - c.-30158A>C r.(?) p.(=)
DCLRE1B NM_022836.3 +/. - c.-3806T>G r.(?) p.(=)


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