Genomic variant #0001953082

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.11316650_11316651del
Reference Copied from the Exome Variant Server
DB-ID AMELX_000013
Frequency 2/10205
Freq. EA 1/6484
Freq. AA 1/3721
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AMELX NM_001142.2 ?/? c.145-18_145-17del r.(=) p.(=)
ARHGAP6 NM_013427.2 ?/? c.589-43824_589-43823del r.(=) p.(=)