Variant #0000009076 (NC_000002.12:g.47414409C>A, NM_000251.2:c.933C>A (MSH2))
Individual ID |
00001758 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.47414409C>A |
Reference |
- |
DB-ID |
MSH2_000028 See all 3 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Claudia Martin-Hospital de Córdoba |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2021-09-17 16:37:09 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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