Variant #0000005977 (NC_000002.12:g.47803319G>C, NC_000002.12(NM_000179.2):c.3173-101G>C (MSH6))
Individual ID |
00000868 |
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.47803319G>C |
Reference |
- |
DB-ID |
MSH6_000001 See all 21 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 |
2019-06-05 13:25:33 -03:00 (-03) |
Date last edited |
2019-06-05 15:40:17 -03:00 (-03) |
Variant on transcripts
Screenings
|
|