Variant #0000927981 (NC_000001.10:g.114441425T>C, NC_000001.10(NM_006594.3):c.1115-2A>G (AP4B1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.114441425T>C
DNA change (hg38) -
Published as AP4B1(NM_006594.5):c.1115-2A>G
ISCN -
DB-ID AP4B1_000011 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
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.-11428A>G r.(?) p.(=)
AP4B1 NM_006594.3 +?/. - c.1115-2A>G r.spl? p.?
PTPN22 NM_015967.5 +?/. - c.-27180A>G r.(?) p.(=)
AP4B1-AS1 NR_037864.1 +?/. - n.368+814T>C r.(?) -


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