Genomic variant #0001973593

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71358498T>C
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000086
Frequency 1/10536
Freq. EA 1/6705
Freq. AA 0/3831
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.1100T>C r.(?) p.(Met367Thr)