Variant #0000000048 (NC_000014.8:g.45658326C>T, NM_020937.2:c.5101C>T (FANCM))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.45658326C>T
Reference -
DB-ID FANCM_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00129 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2018-12-07 11:59:46 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FANCM NM_020937.2 +?/+? 20 c.5101C>T r.(?) p.(Gln1701*)