Variant #0000002678 (NC_000002.12:g.47805798T>C, NC_000002.12(NM_000179.2):c.3646+91T>C (MSH6))
Individual ID |
00000313 |
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.47805798T>C |
Reference |
- |
DB-ID |
MSH6_000004 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 |
2017-12-06 11:55:15 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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