Genomic variant #0000026947

Individual ID 00020189
Chromosome 9
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.97869555G>C
Reference -
DB-ID FANCC_000035
dbSNP ID -
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 0.00017
Allele Count 1
Allele Number 5752
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FANCC NM_000136.2 ?/? - c.1330-4C>G r.spl? p.?
FANCC NM_001243743.1 ?/? - c.1330-4C>G r.spl? p.?
FANCC NM_001243744.1 ?/? - c.*3923C>G r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000001378 DNA SEQ-NG-I 1 - 14 Despoina Kalfakakou