Genomic variant #0001755886

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.36244987C>T
Reference Copied from the Exome Variant Server
DB-ID LIN37_000031
Frequency 218/12330
Freq. EA 3/8340
Freq. AA 215/3990
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
LIN37 NM_019104.2 ?/? c.514C>T r.(?) p.(Pro172Ser)