Genomic variant #0001991568

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.149984444C>T
Reference Copied from the Exome Variant Server
DB-ID CD99L2_000084
Frequency 226/10563
Freq. EA 168/6728
Freq. AA 58/3835
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CD99L2 NM_031462.3 ?/? c.202+36G>A r.(=) p.(=)