Genomic variant #0001955198

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.17744556T>C
Reference Copied from the Exome Variant Server
DB-ID NHS_000061
Frequency 7/10563
Freq. EA 6/6728
Freq. AA 1/3835
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHS NM_198270.2 ?/? c.2267T>C r.(?) p.(Phe756Ser)