Genomic variant #0000000006

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.69552G>C
Reference -
DB-ID OR4F5_000003
dbSNP ID rs2531266
Frequency 0.006369
Allele Count 2
Allele Number 314
Combined Depth 5604
Homozygous 1
Heterozygote 0
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR4F5 NM_001005484.1 ./. - c.462G>C r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin