Genomic variant #0001609292

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.49119046A>C
Reference Copied from the Exome Variant Server
DB-ID SPAG9_000192
Frequency 5/13006
Freq. EA 0/8600
Freq. AA 5/4406
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SPAG9 NM_003971.5 ?/? c.591-34T>G r.(=) p.(=)