Variant #0000000121 (NC_000002.11:g.47657016T>A, NM_000251.2:c.1212T>A (MSH2))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47657016T>A |
Reference |
- |
DB-ID |
MSH2_000004 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Florian Bayersdorfer |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Florian Bayersdorfer |
Date created |
2022-02-14 15:11:57 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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