Genomic variant #0001764566

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.39694786_39694787insGC
Reference Copied from the Exome Variant Server
DB-ID SYCN_000016
Frequency 2/11776
Freq. EA 0/7932
Freq. AA 2/3844
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SYCN NM_001080468.2 ?/? c.108_109insGC r.(?) p.(Thr37Alafs*84)