Genomic variant #0000284688

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.167145142A>G
Reference Copied from the Exome Variant Server
DB-ID SCN9A_000211
Frequency 4568/11860
Freq. EA 3180/8198
Freq. AA 1388/3662
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SCN9A NM_002977.3 ?/? c.1119T>C r.(=) p.(=)