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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