Variant #0000000965 (NC_000016.9:g.123895_245125dup, HBA2(NM_000517.4):c.-99017_*21526dup)
Chromosome |
16 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Duplication |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.123895_245125dup |
Reference |
Shang et al |
DB-ID |
HBA2_000006 See all 2 reported entries |
Frequency |
- |
Variant remarks |
αααα121.2 |
ClassClinical |
Uncertain significance |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |
Variant on transcripts
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