Variant #0000528928 (NC_000006.11:g.43485090C>T, NM_203290.2:c.116C>T (POLR1C))
Chromosome |
6 |
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.43485090C>T |
DNA change (hg38) |
g.43517352C>T |
Published as |
POLR1C(NM_001318876.1):c.116C>T (p.(Ala39Val)), POLR1C(NM_203290.3):c.116C>T (p.A39V) |
ISCN |
- |
DB-ID |
POLR1C_000014 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) |
0.00031 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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