Variant #0000566161 (NC_000019.9:g.13226504_13226505del, NM_001136035.2:c.389_390del (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.13226504_13226505del |
DNA change (hg38) |
g.13115690_13115691del |
Published as |
TRMT1(NM_001136035.4):c.389_390del (p.(Lys130Argfs*3)), TRMT1(NM_017722.4):c.389_390delAA (p.K130Rfs*3), TRMT1(NM_017722.5):c.389_390delAA (p.K130...) |
ISCN |
- |
DB-ID |
TRMT1_000004 See all 4 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_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 |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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