Variant #0000009895 (NC_000005.9:-, MTRR(NM_002454.2):c.904-20_904-19insC, c.904-20_904-19insT)
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
unknown |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MTRR_00055 |
Frequency |
0.625 |
Variant remarks |
Insertion |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |
Variant on transcripts
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