Variant #0000653594 (NC_000001.10:g.114443859G>A, NM_006594.3:c.616C>T (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.114443859G>A
DNA change (hg38) g.113901237G>A
Published as AP4B1(NM_006594.5):c.616C>T (p.R206*)
ISCN -
DB-ID AP4B1_000048 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) 3.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L15 NM_001010922.2 +?/. - c.-13862C>T r.(?) p.(=)
AP4B1 NM_006594.3 +?/. - c.616C>T r.(?) p.(Arg206Ter)
PTPN22 NM_015967.5 +?/. - c.-29614C>T r.(?) p.(=)
DCLRE1B NM_022836.3 +?/. - c.-4350G>A r.(?) p.(=)
AP4B1-AS1 NR_037864.1 +?/. - n.1734G>A r.(?) -


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