Variant #0000546336 (NC_000012.11:g.106820978_106820979dup, NM_018082.5:c.1105_1106dup (POLR3B))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.106820978_106820979dup
DNA change (hg38) g.106427200_106427201dup
Published as POLR3B(NM_001160708.1):c.928_929insTT (p.(Leu311PhefsTer17)), POLR3B(NM_018082.5):c.1105_1106dupTT (p.L369Ffs*17)
ISCN -
DB-ID POLR3B_000043 See all 2 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 18:02:10 +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.1105_1106dup r.(?) p.(Leu369PhefsTer17)


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