Variant #0000347835 (NC_000012.11:g.106821117T>C, NM_018082.5:c.1244T>C (POLR3B))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.106821117T>C |
DNA change (hg38) |
g.106427339T>C |
Published as |
POLR3B(NM_018082.5):c.1244T>C (p.M415T), POLR3B(NM_018082.6):c.1244T>C (p.(Met415Thr), p.M415T) |
ISCN |
- |
DB-ID |
POLR3B_000032 See all 8 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) |
0.00056 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
|