Basic Information
SNP ID | hsa762 |
---|---|
Organism | Homo Sapiens |
Genome Assembly | GRCh37 |
Version | 1 |
Variation Class | SNP |
Position | 1:799463 |
RefSNP Alleles | T/C |
Synonyms ID | rs4245756 |
Gene Annotation
Gene ID | Transcript ID | Gene Symbol | Variant Effect | Biotype | cDNA Position | Allele Change | Protein ID | Protein Position | Residue Change |
---|---|---|---|---|---|---|---|---|---|
ENSG00000228794 | ENST00000445118 | LINC01128 | downstream_gene_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000230368 | ENST00000427857 | FAM41C | downstream_gene_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000230368 | ENST00000432963 | FAM41C | downstream_gene_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000230368 | ENST00000446136 | FAM41C | downstream_gene_variant | lincRNA | 0 | - => - | - | 0 | - => - |
Population Diversity
Population | Sample # | Allele:Frequency | Genotype:Frequency |
---|---|---|---|
EAS | 215 | T:0.00; C:1.00; | CC:1.00; |