Variant #0000856969 (NC_000001.10:g.151378186dup, NM_015100.3:c.3325dup (POGZ))

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.151378186dup
DNA change (hg38) -
Published as POGZ(NM_015100.3):c.3325dupC (p.Q1109Pfs*18)
ISCN -
DB-ID PSMB4_000026
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMB4 NM_002796.2 +/. - c.*3881dup r.(?) p.(=)
POGZ NM_015100.3 +/. - c.3325dup r.(?) p.(Gln1109Profs*18)


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