Variant #0000003911 (NC_000002.12:g.47414419G>A, NC_000002.12(NM_000251.2):c.942+1G>A (MSH2))
Individual ID |
00000219 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.47414419G>A |
Reference |
- |
DB-ID |
MSH2_000024 See all 3 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Carlos Vaccaro-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2018-02-28 09:29:29 -03:00 (-03) |
Date last edited |
2019-12-10 12:43:02 -02:00 (-02) |
Variant on transcripts
Screenings
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