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 |
N/A |
Variant on transcripts
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