View genomic variant #0000000048

Chromosome 14
Allele Unknown
Affects function (reported) Probably affects function
Affects function (concluded) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.45658326C>T
Reference -
DB-ID FANCM_000001
Frequency -
Average frequency (large NGS studies) 0.00038 View details
Owner Florian Bayersdorfer




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*)