Variant #0000003145 (NC_000008.11:g.89947853_89947856delCTTC, NBN(NM_002485.4):c.1882_1885delGAAG)
Individual ID |
00000389 |
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.89947853_89947856delCTTC |
Reference |
- |
DB-ID |
NBN_000002 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Rita Valdez-Hospital Alemán |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Variant on transcripts
Screenings
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