Variant #0000001131 (NC_000016.9:g.97115_175257del)
| Individual ID |
00001972 |
| Chromosome |
16 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Type |
Deletion |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.97115_175257del |
| Reference |
Shang et al |
| DB-ID |
HBA1_000002 See all 2 reported entries |
| Frequency |
- |
| Variant remarks |
-a78 |
| ClassClinical |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Qi Ming |
| Database submission license |
No license selected |
| Created by |
Qi Ming |

Variant on transcripts
Screenings
|
|