Variant #0000502552 (NC_000001.10:g.114441349T>C, NM_006594.3:c.1189A>G (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.114441349T>C
DNA change (hg38) g.113898727T>C
Published as AP4B1(NM_001253852.1):c.1189A>G (p.(Ile397Val))
ISCN -
DB-ID AP4B1_000032
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) 0.00102 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-04 18:52:28 +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.-11352A>G r.(?) p.(=)
AP4B1 NM_006594.3 -?/. - c.1189A>G r.(?) p.(Ile397Val)
PTPN22 NM_015967.5 -?/. - c.-27104A>G r.(?) p.(=)
AP4B1-AS1 NR_037864.1 -?/. - n.368+738T>C r.(?) -


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