Variant #0000174399 (NC_000017.10:g.17129566_17129567delinsGTG, FLCN(NM_144997.5):c.319_320delinsCAC)

Individual ID 00107993
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.17129566_17129567delinsGTG
DNA change (hg38) g.17226252_17226253delinsGTG
Published as 774-5delGTinsCAC
ISCN -
DB-ID FLCN_000008 See all 9 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license No license selected
Created by Derek Lim
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLCN NM_144997.5 +/+ 5 c.319_320delinsCAC r.(?) p.(Val107Hisfs*26)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000108460 DNA ? - - FLCN 1 Johan den Dunnen