Genomic variant #0001764562

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.39694627C>T
Reference Copied from the Exome Variant Server
DB-ID SYCN_000012
Frequency 1/12488
Freq. EA 1/8354
Freq. AA 0/4134
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SYCN NM_001080468.2 ?/? c.268G>A r.(?) p.(Val90Met)