Genomic variant #0001953085

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.11316725G>A
Reference Copied from the Exome Variant Server
DB-ID AMELX_000016
Frequency 1/10563
Freq. EA 0/6728
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.202G>A r.(?) p.(Val68Met)
ARHGAP6 NM_013427.2 ?/? c.589-43898C>T r.(?) p.(Val68Met)