Variant #0000008950 (NC_000007.14:g.116740979A>G, NM_000245.4:c.1655T>C (MET))
Individual ID |
00001638 |
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.116740979A>G |
Reference |
- |
DB-ID |
MET_000005 |
dbSNP ID |
- |
Variant remarks |
NC_000007.14:g.116740979A>G |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Jesica Ramirez-Hospital Central de Mendoza |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2021-07-27 16:06:55 -03:00 (-03) |
Date last edited |
2023-04-28 17:23:10 -03:00 (-03) |
Variant on transcripts
Screenings
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