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;