Genomic variant #0001973569

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71350635G>A
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000068
Frequency 1/9832
Freq. EA 0/6498
Freq. AA 1/3334
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.281-1294G>A r.(=) p.(=)
RGAG4 NM_001024455.3 ?/? c.756C>T r.(=) p.(=)