Variant #0000009690 (NC_000001.10:-, MTR(NM_000254.2):c.2114_2115delTC)
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Exon |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MTR_00027 See all 2 reported entries |
Frequency |
- |
Variant remarks |
c.2112_2113delTC |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
|
|