Variant #0000973292 (NC_000001.10:g.151377425T>G, NM_015100.3:c.4086A>C (POGZ))

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.151377425T>G
DNA change (hg38) -
Published as POGZ(NM_015100.4):c.4086A>C (p.(Glu1362Asp))
ISCN -
DB-ID PSMB4_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) 5.0E-5 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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMB4 NM_002796.2 -?/. - c.*3120T>G r.(=) p.(=)
POGZ NM_015100.3 -?/. - c.4086A>C r.(?) p.(Glu1362Asp)


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