Variant #0000000223 (NC_000019.9:g.12996130C>T, KLF1(NM_006563.3):c.913+1G>A)
Chromosome |
19 |
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.12996130C>T |
Reference |
Liu D,et al |
DB-ID |
KLF1_000019 |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
Likely 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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