Genomic variant #0001973578

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71351356C>T
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000087
Frequency 2/9345
Freq. EA 0/6267
Freq. AA 2/3078
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.281-573C>T r.(?) p.(Arg12His)
RGAG4 NM_001024455.3 ?/? c.35G>A r.(?) p.(Arg12His)