Variant #0000000303 (NC_000011.9:g.5248259_5248262delGTTT, HBB(NM_000518.4):c.-11_-8delAAAC)
Chromosome |
11 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Deletion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5248259_5248262delGTTT |
Reference |
Huang et al;dbSNP |
DB-ID |
HBB_000029 |
Frequency |
- |
Variant remarks |
Cap +43/+40 (-AAAC) |
ClassClinical |
Pathogenic |
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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