Variant #0000946933 (NC_000001.10:g.114439059C>A, NM_006594.3:c.1331G>T (AP4B1))

Chromosome 1
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.114439059C>A
DNA change (hg38) -
Published as AP4B1(NM_006594.5):c.1331G>T (p.G444V)
ISCN -
DB-ID AP4B1_000021 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) 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L15 NM_001010922.2 ?/. - c.-9062G>T r.(?) p.(=)
AP4B1 NM_006594.3 ?/. - c.1331G>T r.(?) p.(Gly444Val)
PTPN22 NM_015967.5 ?/. - c.-24814G>T r.(?) p.(=)
AP4B1-AS1 NR_037864.1 ?/. - n.247-1431C>A r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.