Variant #0000000384 (NC_000011.9:g.5248161T>C, HBB(NM_000518.4):c.91A>G)
| Chromosome |
11 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5248161T>C |
| Reference |
dbSNP;Waye JS et al.; |
| DB-ID |
HBB_000054 See all 2 reported entries |
| Frequency |
- |
| Variant remarks |
IVS-I (-2) or codon 30 (A->G); AG^GTTGGT->GG^GTTGGT Probably beta0 |
| 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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