Basic Information
SNP ID | hsa1413 |
---|---|
Organism | Homo Sapiens |
Genome Assembly | GRCh37 |
Version | 1 |
Variation Class | SNP |
Position | 1:842825 |
RefSNP Alleles | A/G |
Synonyms ID | rs7519340 |
Gene Annotation
Gene ID | Transcript ID | Gene Symbol | Variant Effect | Biotype | cDNA Position | Allele Change | Protein ID | Protein Position | Residue Change |
---|---|---|---|---|---|---|---|---|---|
ENSG00000230699 | ENST00000448179 | RP11-54O7.1 | upstream_gene_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000272438 | ENST00000607769 | RP11-54O7.16 | intron_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000272438 | ENST00000607769 | RP11-54O7.16 | non_coding_transcript_variant | lincRNA | 0 | - => - | - | 0 | - => - |
Population Diversity
Population | Sample # | Allele:Frequency | Genotype:Frequency |
---|---|---|---|
EAS | 215 | A:0.00; G:1.00; | GG:1.00; |