Variant #0000914812 (NC_000009.11:g.97873918A>G, NM_000136.2:c.1156T>C (FANCC))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.97873918A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FANCC_000031
Frequency 27/13006
Freq. EA 0/8600
Freq. AA 27/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:29:58 +02:00 (CEST)
Date last edited 2013-05-04 17:05:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FANCC NM_000136.2 ?/? c.1156T>C r.(?) p.(Ser386Pro)