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 |
2025-08-05 13:42:45 +00:00 (UTC) |

Variant on transcripts
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