Variant #0000001521 (NC_000020.11:g.46007337C>T, NM_004994.2:c.-1590C>T (MMP9))
Individual ID |
00000319 |
Chromosome |
20 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.46007337C>T |
Published as |
C1562T |
Reference |
dbSNP |
DB-ID |
MMP9_000001 See all 4 reported entries |
dbSNP ID |
rs3918242 |
Frequency |
85/133 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nuur Athirah Binti Mohd Daud |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2021-01-05 15:34:36 +08:00 (CST) |
Date last edited |
2021-09-01 11:38:50 +08:00 (CST) |

Variant on transcripts
Screenings
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