Variant #0000000222 (NC_000019.9:g.12996140_12996141insGCGC, KLF1(NM_006563.3):c.903_904insGCGC)
Chromosome |
19 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Insertion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.12996140_12996141insGCGC |
Reference |
Wang T,et al |
DB-ID |
KLF1_000018 |
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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