Variant #0000763538 (NC_000017.10:g.17131297del, FLCN(NM_144997.5):c.155del)

Individual ID 00361883
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.17131297del
DNA change (hg38) -
Published as -
ISCN -
DB-ID FLCN_000316
Variant remarks -
Reference PubMed: Johannesma et al. 2014
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 Kenki Matsumoto
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 +/+ 4 c.155del r.(?) p.(Gln53Argfs*2)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000363112 DNA ? - - FLCN 1 Kenki Matsumoto