Variant #0000502548 (NC_000001.10:g.114438527C>T, NM_006594.3:c.1644G>A (AP4B1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.114438527C>T
DNA change (hg38) g.113895905C>T
Published as AP4B1(NM_006594.4):c.1644G>A (p.P548=)
ISCN -
DB-ID AP4B1_000029
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.-8530G>A r.(?) p.(=)
AP4B1 NM_006594.3 -?/. - c.1644G>A r.(?) p.(Pro548=)
PTPN22 NM_015967.5 -?/. - c.-24282G>A r.(?) p.(=)
AP4B1-AS1 NR_037864.1 -?/. - n.247-1963C>T r.(?) -


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