Variant #0000966669 (NC_000012.11:g.107114642G>A, NM_018082.5:c.*211315G>A (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.107114642G>A
DNA change (hg38) -
Published as RFX4(NM_213594.3):c.1339G>A (p.A447T)
ISCN -
DB-ID POLR3B_000100
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 2024-02-26 20:06:56 +01:00 (CET)
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.*211315G>A r.(=) p.(=)
RIC8B NM_018157.2 ?/. - c.-53882G>A r.(?) p.(=)
RFX4 NM_032491.5 ?/. - c.1057G>A r.(?) p.(Ala353Thr)


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