Genomic variant #0001973566

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71350500C>T
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000062
Frequency 9/9673
Freq. EA 0/6441
Freq. AA 9/3232
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.281-1429C>T r.(=) p.(=)
RGAG4 NM_001024455.3 ?/? c.891G>A r.(=) p.(=)