Basic Information
SNP ID | hsa822 |
---|---|
Organism | Homo Sapiens |
Genome Assembly | GRCh37 |
Version | 1 |
Variation Class | SNP |
Position | 1:812751 |
RefSNP Alleles | T/C |
Synonyms ID | rs4246500 |
Gene Annotation
Gene ID | Transcript ID | Gene Symbol | Variant Effect | Biotype | cDNA Position | Allele Change | Protein ID | Protein Position | Residue Change |
---|---|---|---|---|---|---|---|---|---|
ENSG00000230368 | ENST00000427857 | FAM41C | upstream_gene_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000230368 | ENST00000446136 | FAM41C | upstream_gene_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000234711 | ENST00000415481 | TUBB8P11 | downstream_gene_variant | unprocessed_pseudogene | 0 | - => - | - | 0 | - => - |
Population Diversity
Population | Sample # | Allele:Frequency | Genotype:Frequency |
---|---|---|---|
EAS | 215 | T:0.00; C:1.00; | CC:1.00; |