Variant #0000009663 (NC_000001.10:-, MTR(NM_000254.2):c.1516-93T>A, c.1516-93T>C)
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Intron |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MTR_00163 |
Frequency |
0.500 |
Variant remarks |
- |
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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