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 International |
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) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|