Genomic variant #0000209070

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.69761A>T
Reference dbSNP
DB-ID OR4F5_000004
Frequency 0.038
Allele Count 3
Allele Number 78
Depth 102
Average frequency (large NGS studies) 0.09254 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