Variant #0000392559 (NC_000003.11:g.60898423C>T, NC_000003.11(NM_002012.2):c.-110-90718G>A (FHIT))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.60898423C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FHIT_000071
Frequency 23/5734
Freq. EA 0/3982
Freq. AA 23/1752
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 16:23:53 +02:00 (CEST)
Date last edited 2013-05-04 02:33:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FHIT NM_002012.2 ?/? c.-110-90718G>A r.(=) p.(=)