Genomic variant #0001444988

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.1503879T>A
Reference Copied from the Exome Variant Server
DB-ID CLCN7_000140
Frequency 6620/12998
Freq. EA 4312/8600
Freq. AA 2308/4398
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CLCN7 NM_001287.5 ?/? c.1170A>T r.(=) p.(=)