Variant #0000008514 (NC_000007.13:-, MET(NM_001127500.1):c.-187-u529A>C)
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
The SNP conversion shows 'g.4472A>C' (c.1-729A>C), but in the reference sequence, c.1-729 is G. |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MET_00043 |
Frequency |
- |
Variant remarks |
Substitution |
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
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