Variant #0001038909 (NC_000012.11:g.107080781_107080783del, NM_018082.5:c.*177454_*177456del (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.107080781_107080783del
DNA change (hg38) -
Published as RFX4(NM_213594.3):c.497_499del (p.(Val166del))
ISCN -
DB-ID POLR3B_000121
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 2025-05-05 21:14:00 +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     
POLR3B NM_018082.5 ?/. - c.*177454_*177456del r.(=) p.(=)
RIC8B NM_018157.2 ?/. - c.-87743_-87741del r.(?) p.(=)
RFX4 NM_032491.5 ?/. - c.215_217del r.(?) p.(Val72del)


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