Variant #0000262560 (NC_000001.10:g.114441378_114441379del, NM_006594.3:c.1160_1161del (AP4B1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.114441378_114441379del
DNA change (hg38) g.113898756_113898757del
Published as AP4B1(NM_006594.4):c.1160_1161delCA (p.T387Rfs*30)
ISCN -
DB-ID AP4B1_000010 See all 3 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +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.-11381_-11380del r.(?) p.(=)
AP4B1 NM_006594.3 +/. - c.1160_1161del r.(?) p.(Thr387ArgfsTer30)
PTPN22 NM_015967.5 +/. - c.-27133_-27132del r.(?) p.(=)
AP4B1-AS1 NR_037864.1 +/. - n.368+767_368+768del r.(?) -


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