Basic Information

SNP ID hsa1434
Organism Homo Sapiens
Genome Assembly GRCh37
Version 1
Variation Class SNP
Position 1:847250
RefSNP Alleles G/A
Synonyms ID rs7416129

Gene Annotation

Gene ID Transcript ID Gene Symbol Variant Effect Biotype cDNA Position Allele Change Protein ID Protein Position Residue Change
ENSG00000223764 ENST00000417705 RP11-54O7.3 downstream_gene_variant lincRNA 0 - => - - 0 - => -
ENSG00000223764 ENST00000609207 RP11-54O7.3 downstream_gene_variant retained_intron 0 - => - - 0 - => -
ENSG00000241180 ENST00000398216 RP11-54O7.2 upstream_gene_variant lincRNA 0 - => - - 0 - => -
ENSG00000272438 ENST00000607769 RP11-54O7.16 intron_variant lincRNA 0 - => - - 0 - => -
ENSG00000230699 ENST00000448179 RP11-54O7.1 intron_variant lincRNA 0 - => - - 0 - => -
ENSG00000272438 ENST00000607769 RP11-54O7.16 non_coding_transcript_variant lincRNA 0 - => - - 0 - => -
ENSG00000230699 ENST00000448179 RP11-54O7.1 non_coding_transcript_variant lincRNA 0 - => - - 0 - => -

Population Diversity

Population Sample # Allele:Frequency Genotype:Frequency
EAS 215 G:0.00; A:1.00; AA:1.00;