Genomic variant #0001973592

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71358473C>T
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000084
Frequency 1/10476
Freq. EA 0/6666
Freq. AA 1/3810
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.1075C>T r.(?) p.(Arg359Trp)