Genomic variant #0001609291

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.49119038C>T
Reference Copied from the Exome Variant Server
DB-ID SPAG9_000191
Frequency 3/13004
Freq. EA 2/8598
Freq. AA 1/4406
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SPAG9 NM_003971.5 ?/? c.591-26G>A r.(=) p.(=)