Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
117801 BAA10g10750 A10 12493559 C T upstream_gene_variant MODIFIER c.-3654C>T| S301
S304
117802 BAA10g10750 A10 12493681 G A upstream_gene_variant MODIFIER c.-3532G>A| S192
117803 BAA10g10750 A10 12494073 G A upstream_gene_variant MODIFIER c.-3140G>A| S251
117804 BAA10g10750 A10 12494191 G A upstream_gene_variant MODIFIER c.-3022G>A| S57
117805 BAA10g10750 A10 12495277 G A upstream_gene_variant MODIFIER c.-1936G>A| S288
117806 BAA10g10750 A10 12496786 G A upstream_gene_variant MODIFIER c.-427G>A| S263
117807 BAA10g10750 A10 12497520 G A missense_variant MODERATE c.157G>A|p.Val53Ile S178
117808 BAA10g10750 A10 12497664 C T missense_variant MODERATE c.301C>T|p.Pro101Ser S281
117809 BAA10g10750 A10 12498591 G A downstream_gene_variant MODIFIER c.*808G>A| S13
117810 BAA10g10750 A10 12499120 C T downstream_gene_variant MODIFIER c.*1337C>T| S42
117811 BAA10g10750 A10 12500462 G A downstream_gene_variant MODIFIER c.*2679G>A| S95
117812 BAA10g10760 A10 12501934 G A upstream_gene_variant MODIFIER c.-3705G>A| S71
117813 BAA10g10760 A10 12502388 C T upstream_gene_variant MODIFIER c.-3251C>T| S149
117814 BAA10g10760 A10 12502523 C T upstream_gene_variant MODIFIER c.-3116C>T| S8
117815 BAA10g10760 A10 12504323 A G upstream_gene_variant MODIFIER c.-1316A>G| S284
117816 BAA10g10760 A10 12504386 C T upstream_gene_variant MODIFIER c.-1253C>T| S123
117817 BAA10g10760 A10 12504783 G A upstream_gene_variant MODIFIER c.-856G>A| S289
117818 BAA10g10760 A10 12505374 G A upstream_gene_variant MODIFIER c.-265G>A| S255
117819 BAA10g10760 A10 12507137 C T downstream_gene_variant MODIFIER c.*928C>T| S123
117820 BAA10g10760 A10 12507608 C T downstream_gene_variant MODIFIER c.*1399C>T| S294
117821 BAA10g10760 A10 12508453 G A downstream_gene_variant MODIFIER c.*2244G>A| S245
117822 BAA10g10760 A10 12508603 C T downstream_gene_variant MODIFIER c.*2394C>T| S133
117823 BAA10g10760 A10 12508891 C T downstream_gene_variant MODIFIER c.*2682C>T| S68
117824 BAA10g10760 A10 12508930 G A downstream_gene_variant MODIFIER c.*2721G>A| S241
117825 BAA10g10760 A10 12509314 G A downstream_gene_variant MODIFIER c.*3105G>A| S35