Variant #0000010065 (NC_000017.11:g.?, NM_144997.6:Deletion (Exon 1) (FLCN))
Individual ID |
00002998 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.? |
Reference |
- |
DB-ID |
TP53_000027 See all 8 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Pablo Kalfayan-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2024-07-18 17:56:43 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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