Variant #0000000091 (NC_000011.9:g.67257602C>T, NM_003977.2:c.562C>T (AIP))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.67257602C>T |
Reference |
- |
DB-ID |
AIP_000002 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
Owner |
Florian Bayersdorfer |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Florian Bayersdorfer |
Date created |
2020-03-03 13:47:17 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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