Variant #0001321356 (NC_000014.8:g.45658326C>T, NM_020937.2:c.5101C>T (FANCM))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.45658326C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FANCM_000243
Frequency 5/13006
Freq. EA 5/8600
Freq. AA 0/4406
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 16:41:19 +02:00 (CEST)
Date last edited 2013-05-05 07:18:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FANCM NM_020937.2 ?/? c.5101C>T r.(?) p.(Gln1701*)