Variant #0000000982 (NC_000016.9:g.220831_232003del, HBA2(NM_000517.4):c.-2081_*8404del)
Chromosome |
16 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Deletion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.220831_232003del |
Reference |
Xu et al |
DB-ID |
HBA2_000003 See all 4 reported entries |
Frequency |
- |
Variant remarks |
- -11.1 |
ClassClinical |
Pathogenic |
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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