Variant #0000016125 (NC_000002.11:g.60689441A>G, BCL11A(NM_022893.3):c.606A>G)
| Individual ID |
00002099 |
| Chromosome |
2 |
| 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.60689441A>G |
| Reference |
Shang et al.(2017),dbSNP |
| DB-ID |
BCL11A_000001 See all 3 reported entries |
| Frequency |
- |
| Variant remarks |
Elevated HbF |
| ClassClinical |
Likely benign |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Qianqian Zhang |
| Database submission license |
No license selected |
| Created by |
Qianqian Zhang |

Variant on transcripts
Screenings
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