Variant #0000002656 (NC_000002.12:g.47806273T>C, NM_000179.2:c.3716T>C (MSH6))
Individual ID |
00000312 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.47806273T>C |
Reference |
- |
DB-ID |
MSH6_000024 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Lina Nuñez-Private Practice |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2017-11-17 15:46:48 -02:00 (-02) |
Date last edited |
2023-04-27 15:17:40 -03:00 (-03) |
Variant on transcripts
Screenings
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