Variant #0000000588 (NC_000011.9:g.5247905_5247906insT, HBB(NM_000518.4):c.216_217insA)
Individual ID |
00000713, 00000745, 00001260 |
Chromosome |
11 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Insertion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5247905_5247906insT |
Reference |
(OMIM 0328);dbSNP;Chen et al. |
DB-ID |
HBB_000112 See all 2 reported entries |
Frequency |
- |
Variant remarks |
Codons 71/72 (+A) |
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
Screenings
|
|