Variant #0000001047 (NC_000016.9:g.1_282199dup, HBA1(NM_000558.3):c.-226715_*54789dup)
Chromosome |
16 |
Allele |
Parent #1 |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Type |
Duplication |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1_282199dup |
Reference |
Hu et al |
DB-ID |
HBA2_000040 See all 2 reported entries |
Frequency |
- |
Variant remarks |
αααα282.1 |
ClassClinical |
Uncertain significance |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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