Genomic variant #0000003595

Individual ID 00016360
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.98011497G>A
Reference -
DB-ID FANCC_000007 See all 39 reported entries
dbSNP ID rs1800361
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 0.00661
Allele Count 38
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.77C>T r.(?) p.(Ser26Phe)
FANCC NM_001243743.1 ?/? - c.77C>T r.(?) p.(Ser26Phe)
FANCC NM_001243744.1 ?/? - c.77C>T r.(?) p.(Ser26Phe)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000000088 DNA SEQ-NG-I 1 - 6 Despoina Kalfakakou