Genomic variant #0000982271

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.32128611A>G
Reference Copied from the Exome Variant Server
DB-ID ARHGAP12_000083
Frequency 2195/13006
Freq. EA 1824/8600
Freq. AA 371/4406
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP12 NM_001270695.1 ?/? c.1325T>C r.(?) p.(Phe442Ser)