Genomic variant #0000020146

Individual ID 00016942
Chromosome 11
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.22647116C>A
Reference -
DB-ID FANCF_000002 See all 15 reported entries
dbSNP ID rs145057187
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 0.00261
Allele Count 15
Allele Number 5752
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FANCF NM_022725.3 ?/? - c.241G>T r.(?) p.(Ala81Ser)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000000709 DNA SEQ-NG-I 1 - 14 Despoina Kalfakakou