Variant #0001563393 (NC_000017.10:g.17129486T>C, NC_000017.10(NM_144606.5):c.396+4A>G (FLCN))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.17129486T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FLCN_000090
Frequency 4/13006
Freq. EA 4/8600
Freq. AA 0/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:44:12 +02:00 (CEST)
Date last edited 2017-08-09 13:37:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FLCN NM_144606.5 ?/? c.396+4A>G r.spl? p.?