Genomic variant #0001973554

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71350133T>G
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000054
Frequency 656/10282
Freq. EA 578/6597
Freq. AA 78/3685
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.281-1796T>G r.(?) p.(Ser420Arg)
RGAG4 NM_001024455.3 ?/? c.1258A>C r.(?) p.(Ser420Arg)