Genomic variant #0001973508

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71342006A>G
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000004
Frequency 3511/3599
Freq. EA 2389/2390
Freq. AA 1122/1209
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.281-9923A>G r.(=) p.(=)