Variant #0000798771 (NC_000001.10:g.151377576A>C, NM_015100.3:c.3935T>G (POGZ))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.151377576A>C
DNA change (hg38) -
Published as POGZ(NM_001194937.2):c.3908T>G (p.I1303S)
ISCN -
DB-ID PSMB4_000021
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMB4 NM_002796.2 +?/. - c.*3271A>C r.(=) p.(=)
POGZ NM_015100.3 +?/. - c.3935T>G r.(?) p.(Ile1312Ser)


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