Variant #0000006836 (NC_000017.11:g.17224157G>A, NM_144997.6:c.397-14C>T (FLCN))
Individual ID |
00001161 |
Chromosome |
17 |
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.17224157G>A |
Reference |
- |
DB-ID |
FLCN_000002 See all 2 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Lina Nuñez-Private Practice |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-05-18 15:41:26 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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