Basic Information
SNP ID | hsa37 |
---|---|
Organism | Homo Sapiens |
Genome Assembly | GRCh37 |
Version | 1 |
Variation Class | SNP |
Position | 1:66507 |
RefSNP Alleles | T/A |
Synonyms ID | rs12401368 |
Gene Annotation
Gene ID | Transcript ID | Gene Symbol | Variant Effect | Biotype | cDNA Position | Allele Change | Protein ID | Protein Position | Residue Change |
---|---|---|---|---|---|---|---|---|---|
ENSG00000186092 | ENST00000335137 | OR4F5 | upstream_gene_variant | mRNA | 0 | - => - | ENSP00000334393 | 0 | - => - |
ENSG00000240361 | ENST00000492842 | OR4G11P | downstream_gene_variant | unprocessed_pseudogene | 0 | - => - | - | 0 | - => - |
Population Diversity
Population | Sample # | Allele:Frequency | Genotype:Frequency |
---|---|---|---|
EAS | 215 | T:0.54; A:0.46; | AA:0.27; AT:0.45; TT:0.27; |