Variant #0000000059 (NC_000019.9:g.12996519_12996525dupGGCGCCG, KLF1(NM_006563.3):c.519_525dupCGGCGCC)
Individual ID |
00000120, 00000425, 00000461, 00000706, 00000707, 00000718, 00000796, 00001189, 00001338, 00001530, 00001570, 00001583, 00001637, 00001639, 00001675, 00001701, 00001702, 00001703, 00001706, 00001707, 00001715 |
Chromosome |
19 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Duplication |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.12996519_12996525dupGGCGCCG |
Reference |
GenBank |
DB-ID |
KLF1_000002 See all 2 reported entries |
Frequency |
- |
Variant remarks |
Elevated HbF |
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
Screenings
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