Genomic variant #0000512938

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.141334151T>C
Reference Copied from the Exome Variant Server
DB-ID CLGN_000120
Frequency 1/13004
Freq. EA 0/8598
Freq. AA 1/4406
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CLGN NM_004362.2 ?/? c.82A>G r.(?) p.(Thr28Ala)