Variant #0000000057 (NC_000002.11:g.47643434G>A, NC_000002.11(NM_000251.2):c.943-1G>A (MSH2))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47643434G>A |
Reference |
- |
DB-ID |
MSH2_000003 |
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 |
2018-12-07 13:33:03 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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