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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