Genomic variant #0000209069

Individual ID 00000003
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.69511A>G
Reference dbSNP
DB-ID OR4F5_000003
Frequency 0.857
Allele Count 108
Allele Number 126
Depth 3898
Average frequency (large NGS studies) 0.75977 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
OR4F5 NM_001005484.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin