Basic Information
SNP ID | hsa803 |
---|---|
Organism | Homo Sapiens |
Genome Assembly | GRCh37 |
Version | 1 |
Variation Class | SNP |
Position | 1:807512 |
RefSNP Alleles | A/G |
Synonyms ID | rs10751454 |
Gene Annotation
Gene ID | Transcript ID | Gene Symbol | Variant Effect | Biotype | cDNA Position | Allele Change | Protein ID | Protein Position | Residue Change |
---|---|---|---|---|---|---|---|---|---|
ENSG00000230368 | ENST00000427857 | FAM41C | intron_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000230368 | ENST00000427857 | FAM41C | non_coding_transcript_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000230368 | ENST00000432963 | FAM41C | upstream_gene_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000230368 | ENST00000446136 | FAM41C | intron_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000230368 | ENST00000446136 | FAM41C | non_coding_transcript_variant | lincRNA | 0 | - => - | - | 0 | - => - |
ENSG00000234711 | ENST00000415481 | TUBB8P11 | upstream_gene_variant | unprocessed_pseudogene | 0 | - => - | - | 0 | - => - |
Population Diversity
Population | Sample # | Allele:Frequency | Genotype:Frequency |
---|---|---|---|
EAS | 215 | A:0.00; G:1.00; | GG:1.00; |