Variant #0000502553 (NC_000001.10:g.114442672G>A, NM_006594.3:c.968C>T (AP4B1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.114442672G>A
DNA change (hg38) g.113900050G>A
Published as AP4B1(NM_006594.4):c.968C>T (p.S323L)
ISCN -
DB-ID AP4B1_000022 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) 0.0006 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 2020-06-04 18:53:50 +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.-12675C>T r.(?) p.(=)
AP4B1 NM_006594.3 ?/. - c.968C>T r.(?) p.(Ser323Leu)
PTPN22 NM_015967.5 ?/. - c.-28427C>T r.(?) p.(=)
DCLRE1B NM_022836.3 ?/. - c.-5537G>A r.(?) p.(=)
AP4B1-AS1 NR_037864.1 ?/. - n.547G>A r.(?) -


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