Variant #0001530116 (NC_000016.9:g.89866102_89866103insC, NC_000016.9(NM_000135.2):c.793-57_793-56insG (FANCA))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.89866102_89866103insC
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FANCA_000527
Frequency 1/12518
Freq. EA 1/8254
Freq. AA 0/4264
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 16:42:42 +02:00 (CEST)
Date last edited 2018-01-11 08:48:09 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FANCA NM_000135.2 ?/? c.793-57_793-56insG r.(=) p.(=)