Variant #0000761106 (NC_000017.10:g.17129563C>A, NM_144997.5:c.323G>T (FLCN))
Individual ID |
00359764 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17129563C>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
FLCN_000113 See all 2 reported entries |
Variant remarks |
- |
Reference |
PubMed: Benusiglio et al. 2014 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Kenki Matsumoto |
Database submission license |
No license selected |
Created by |
Derek Lim |
Date created |
2021-04-04 15:47:15 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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