Variant #0000000298 (NC_000011.9:g.2182523_2182540delinsACGAT, NM_000207.2:c.-160_-143delinsATCGT (INS))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2182523_2182540delinsACGAT |
| Reference |
- |
| DB-ID |
INS_000001 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Florian Bayersdorfer |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Florian Bayersdorfer |
| Date created |
2023-06-29 13:36:32 +00:00 (UTC) |
| Date last edited |
2025-11-17 14:32:07 +00:00 (UTC) |

Variant on transcripts
|