Genomic variant #0000019890

Individual ID 00016926
Chromosome 17
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.17119729G>A
Reference -
DB-ID FLCN_000020 See all 3 reported entries
dbSNP ID rs565447853
Variant remarks -
Genetic origin Germline
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Variant not found in online data sets
Average frequency in greek population 0.00052
Allele Count 3
Allele Number 5778
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLCN NM_144606.5 ?/? - c.*4964C>T r.(=) p.(=)
FLCN NM_144997.5 ?/? - c.1265C>T r.(?) p.(Pro422Leu)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000000691 DNA SEQ-NG-I 1 - 6 Despoina Kalfakakou