Genomic variant #0001955228

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.17745771C>T
Reference Copied from the Exome Variant Server
DB-ID NHS_000091
Frequency 23/10563
Freq. EA 0/6728
Freq. AA 23/3835
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHS NM_198270.2 ?/? c.3482C>T r.(?) p.(Pro1161Leu)