Variant #0000716700 (NC_000001.10:g.114438446G>A, NM_006594.3:c.1725C>T (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.114438446G>A
DNA change (hg38) -
Published as AP4B1(NM_006594.4):c.1725C>T (p.I575=)
ISCN -
DB-ID AP4B1_000058
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) 0.00054 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L15 NM_001010922.2 -?/. - c.-8449C>T r.(?) p.(=)
AP4B1 NM_006594.3 -?/. - c.1725C>T r.(?) p.(Ile575=)
PTPN22 NM_015967.5 -?/. - c.-24201C>T r.(?) p.(=)
AP4B1-AS1 NR_037864.1 -?/. - n.247-2044G>A r.(?) -


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