Genomic variant #0001995338

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.153222835G>C
Reference Copied from the Exome Variant Server
DB-ID HCFC1_000132
Frequency 1196/10325
Freq. EA 947/6595
Freq. AA 249/3730
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HCFC1 NM_005334.2 ?/? c.2283C>G r.(=) p.(=)