Genomic variant #0001973589

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71358327C>G
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000080
Frequency 1/3600
Freq. EA 1/2391
Freq. AA 0/1209
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.929C>G r.(?) p.(Ser310Cys)