Variant #0001048424 (NC_000019.9:g.13215902G>A, NC_000019.9(NM_001136035.2):c.1834-7C>T (TRMT1))
Chromosome |
19 |
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.13215902G>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
TRMT1_000013 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs2513065519 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2025-09-30 07:20:02 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|