Variant #0000000698 (NC_000018.9:g.2940684T>C, NM_014646.2:c.617A>G (LPIN2))
| Chromosome |
18 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2940684T>C |
| Reference |
- |
| DB-ID |
LPIN2_000006 |
| 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 |
2025-10-06 08:59:49 +00:00 (UTC) |
| Date last edited |
N/A |

Variant on transcripts
|
|