Genomic variant #0000000005

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.69511A>G
Reference -
DB-ID OR4F5_000002
dbSNP ID rs2691305
Frequency 0.9
Allele Count 279
Allele Number 310
Combined Depth 7393
Homozygous 132
Heterozygote 15
Average frequency (large NGS studies) 0.75977 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR4F5 NM_001005484.1 ./. - c.421A>G r.(?) p.(Thr141Ala)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin