Variant #0000000600 (NC_000011.9:g.17436147G>A, NM_000352.3:c.2302C>T (ABCC8))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17436147G>A |
Reference |
- |
DB-ID |
ABCC8_000005 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
Admin |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Admin |
Date created |
2024-07-29 06:05:55 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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