Genomic variant #0001952963

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.11133129T>C
Reference Copied from the Exome Variant Server
DB-ID HCCS_000014
Frequency 12/10563
Freq. EA 0/6728
Freq. AA 12/3835
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HCCS NM_001122608.2 ?/? c.252+23T>C r.(=) p.(=)