Genomic variant #0000000004

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.69428T>G
Reference -
DB-ID OR4F5_000001
dbSNP ID rs140739101
Frequency 0.016
Allele Count 5
Allele Number 322
Combined Depth 4270
Homozygous 2
Heterozygote 1
Average frequency (large NGS studies) 0.03065 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR4F5 NM_001005484.1 ./. - c.338T>G r.(?) p.(Phe113Cys)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin