Genomic variant #0001953071

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.11313027T>C
Reference Copied from the Exome Variant Server
DB-ID AMELX_000002
Frequency 2703/3600
Freq. EA 1658/2391
Freq. AA 1045/1209
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AMELX NM_001142.2 ?/? c.54+65T>C r.(=) p.(=)
ARHGAP6 NM_013427.2 ?/? c.589-40200A>G r.(=) p.(=)