Variant #0000000201 (NC_000002.11:g.60738508A>G, BCL11A(NM_022893.3):c.385+34598T>C)
| 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.60738508A>G |
| Reference |
Yunli Lai,et al ;dbSNP |
| DB-ID |
BCL11A_000008 |
| Frequency |
- |
| Variant remarks |
- |
| ClassClinical |
Likely benign |
| 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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