Variant #0000000534 (NC_000016.9:g.3299468C>T, NM_000243.2:c.1223G>A (MEFV))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.3299468C>T |
| Reference |
https://www.ncbi.nlm.nih.gov/clinvar/variation/974964/ |
| DB-ID |
MEFV_000012 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0.01322 View details |
| Owner |
Florian Bayersdorfer |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Florian Bayersdorfer |
| Date created |
2024-05-07 13:46:45 +00:00 (UTC) |
| Date last edited |
2025-07-29 10:45:33 +00:00 (UTC) |

Variant on transcripts
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