Genomic variant #0001609298

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.49124758A>C
Reference Copied from the Exome Variant Server
DB-ID SPAG9_000198
Frequency 1/13002
Freq. EA 0/8596
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.568T>G r.(?) p.(Ser190Ala)