Genomic variant #0001953074

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.11316205T>C
Reference Copied from the Exome Variant Server
DB-ID AMELX_000005
Frequency 13/10563
Freq. EA 12/6728
Freq. AA 1/3835
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AMELX NM_001142.2 ?/? c.103-151T>C r.(=) p.(=)
ARHGAP6 NM_013427.2 ?/? c.589-43378A>G r.(=) p.(=)