Genomic variant #0000512906

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.141321755T>C
Reference Copied from the Exome Variant Server
DB-ID CLGN_000088
Frequency 1/7262
Freq. EA 1/4608
Freq. AA 0/2654
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CLGN NM_004362.2 ?/? c.502-52A>G r.(=) p.(=)