Variant #0000006860 (NC_000002.12:g.47798625C>T, NM_000179.2:c.642C>T (MSH6))
Individual ID |
00001172 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.47798625C>T |
Reference |
- |
DB-ID |
MSH6_000018 See all 12 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Pablo Kalfayan-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-06-01 17:05:28 -03:00 (-03) |
Date last edited |
N/A |
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Variant on transcripts
Screenings
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