Basic Information
SNP ID | hsa22 |
---|---|
Organism | Homo Sapiens |
Genome Assembly | GRCh37 |
Version | 1 |
Variation Class | SNP |
Position | 1:55545 |
RefSNP Alleles | C/T |
Synonyms ID | rs28396308 |
Gene Annotation
Gene ID | Transcript ID | Gene Symbol | Variant Effect | Biotype | cDNA Position | Allele Change | Protein ID | Protein Position | Residue Change |
---|---|---|---|---|---|---|---|---|---|
ENSG00000268020 | ENST00000594647 | OR4G4P | downstream_gene_variant | unprocessed_pseudogene | 0 | - => - | - | 0 | - => - |
ENSG00000268020 | ENST00000606857 | OR4G4P | downstream_gene_variant | unprocessed_pseudogene | 0 | - => - | - | 0 | - => - |
Population Diversity
Population | Sample # | Allele:Frequency | Genotype:Frequency |
---|---|---|---|
EAS | 215 | C:0.90; T:0.10; | CC:0.80; CT:0.19; TT:0.01; |