Genomic variant #0001973562

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71350294A>G
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000058
Frequency 57/9974
Freq. EA 0/6522
Freq. AA 57/3452
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.281-1635A>G r.(?) p.(Met366Thr)
RGAG4 NM_001024455.3 ?/? c.1097T>C r.(?) p.(Met366Thr)