Genomic variant #0001973595

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71358641G>C
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000089
Frequency 3/10563
Freq. EA 3/6728
Freq. AA 0/3835
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.1243G>C r.(?) p.(Gly415Arg)