Variant #0000004214 (NC_000002.12:g.47791175T>A, NC_000002.12(NM_000179.2):c.457+52T>A (MSH6))
Individual ID |
00000534 |
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.47791175T>A |
Reference |
- |
DB-ID |
MSH6_000009 See all 13 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 |
2018-06-06 11:01:34 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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