Genomic variant #0001973526

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71344119del
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000025
Frequency 8/5743
Freq. EA 4/3545
Freq. AA 4/2198
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.281-7810del r.(=) p.(=)