Variant #0000299055 (NC_000012.11:g.106826199T>A, NM_018082.5:c.1568T>A (POLR3B))

Chromosome 12
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.106826199T>A
DNA change (hg38) g.106432421T>A
Published as POLR3B(NM_018082.5):c.1568T>A (p.V523E, p.(Val523Glu)), POLR3B(NM_018082.6):c.1568T>A (p.V523E)
ISCN -
DB-ID POLR3B_000005 See all 76 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) 0.00028 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLR3B NM_018082.5 +/. - c.1568T>A r.(?) p.(Val523Glu)


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