Variant #0000009893 (NC_000009.12:g.95172033T>A, NC_000009.12(NM_000136.2):c.456+4A>T (FANCC))
Individual ID |
00002754 |
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.95172033T>A |
Reference |
- |
DB-ID |
FANCC_000007 |
dbSNP ID |
rs104886456 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Guillermo Alberto-Instituto Fleming |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2024-03-07 15:58:31 -03:00 (-03) |
Date last edited |
N/A |
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Variant on transcripts
Screenings
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