Variant #0000000023 (NC_000002.11:g.47630397T>C, NM_000251.2:c.67T>C (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.47630397T>C |
| Reference |
- |
| DB-ID |
MSH2_000001 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00065 View details |
| Owner |
Florian Bayersdorfer |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Florian Bayersdorfer |
| Date created |
2017-05-15 10:31:28 +00:00 (UTC) |
| Date last edited |
N/A |

Variant on transcripts
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