Variant #0000006902 (NC_000002.12:g.47476492C>T, NM_000251.2:c.2131C>T (MSH2))
Individual ID |
00001183 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.47476492C>T |
Reference |
- |
DB-ID |
MSH2_000020 See all 5 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Pablo Kalfayan-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-06-05 13:11:09 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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