Variant #0000000388 (NC_000011.9:g.5248159C>A, HBB(NM_000518.4):c.92+1G>T)
Individual ID |
00000017, 00000738 |
Chromosome |
11 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5248159C>A |
Reference |
(OMIM 0347);dbSNP;Chen et al. |
DB-ID |
HBB_000058 See all 2 reported entries |
Frequency |
- |
Variant remarks |
IVS-I-1 (G->T) |
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
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