Variant #0000999583 (NC_000012.11:g.106890589del, NM_018082.5:c.2877del (POLR3B))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.106890589del
DNA change (hg38) -
Published as POLR3B(NM_018082.5):c.2877delC (p.(Tyr960fs))
ISCN -
DB-ID POLR3B_000111
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLR3B NM_018082.5 ?/. - c.2877del r.(?) p.(Tyr960Thrfs*10)
RIC8B NM_018157.2 ?/. - c.-277935del r.(?) p.(=)
RFX4 NM_032491.5 ?/. - c.-188003del r.(?) p.(=)


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