Variant #0001045927 (NC_000003.11:g.48508793G>C, NM_016381.4:c.904G>C (TREX1))
| Chromosome |
3 |
| 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.48508793G>C |
| DNA change (hg38) |
- |
| Published as |
TREX1(NM_007248.4):c.709G>C (p.A237P), TREX1(NM_007248.5):c.709G>C (p.A237P), TREX1(NM_033629.6):c.739G>C (p.(Ala247Pro), p.A247P) |
| ISCN |
- |
| DB-ID |
TREX1_000056 See all 6 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) |
0.00011 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2025-07-08 13:22:38 +02:00 (CEST) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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