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
113801 BAA10g08990 A10 11080474 C T synonymous_variant LOW c.330C>T|p.Phe110Phe S282
113802 BAA10g08990 A10 11080514 C T synonymous_variant LOW c.370C>T|p.Leu124Leu S275
113803 BAA10g08980 A10 11081136 C T upstream_gene_variant MODIFIER c.-3195G>A| S131
113804 BAA10g08980 A10 11081510 G A upstream_gene_variant MODIFIER c.-3569C>T| S219
113805 BAA10g08980 A10 11081521 G A upstream_gene_variant MODIFIER c.-3580C>T| S163
113806 BAA10g08980 A10 11081615 C T upstream_gene_variant MODIFIER c.-3674G>A| S185
113807 BAA10g08980 A10 11081629 C T upstream_gene_variant MODIFIER c.-3688G>A| S247
113808 BAA10g08980 A10 11081987 C T upstream_gene_variant MODIFIER c.-4046G>A| S259
113809 BAA10g08980 A10 11082082 G A upstream_gene_variant MODIFIER c.-4141C>T| S66
113810 BAA10g08980 A10 11082145 C T upstream_gene_variant MODIFIER c.-4204G>A| S269
113811 BAA10g09000 A10 11083452 C T upstream_gene_variant MODIFIER c.-383C>T| S51
113812 BAA10g09000 A10 11084557 G A missense_variant MODERATE c.544G>A|p.Asp182Asn S217
113813 BAA10g09010 A10 11084741 C T upstream_gene_variant MODIFIER c.-1016C>T| S229
113814 BAA10g09010 A10 11084990 C T upstream_gene_variant MODIFIER c.-767C>T| S270
113815 BAA10g09010 A10 11085782 G A missense_variant MODERATE c.26G>A|p.Gly9Glu S216
113816 BAA10g09010 A10 11085834 G A synonymous_variant LOW c.78G>A|p.Ala26Ala S165
113817 BAA10g09030 A10 11087489 G A upstream_gene_variant MODIFIER c.-1718G>A| S125
113818 BAA10g09020 A10 11088181 G A upstream_gene_variant MODIFIER c.-299C>T| S280
113819 BAA10g09020 A10 11088935 G A upstream_gene_variant MODIFIER c.-1053C>T| S74
113820 BAA10g09030 A10 11089603 C T synonymous_variant LOW c.153C>T|p.Asn51Asn S96
113821 BAA10g09030 A10 11091288 G A missense_variant MODERATE c.256G>A|p.Glu86Lys S1
S90
113822 BAA10g09020 A10 11092806 G A upstream_gene_variant MODIFIER c.-4924C>T| S5
113823 BAA10g09030 A10 11095132 G A downstream_gene_variant MODIFIER c.*3824G>A| S198
113824 BAA10g09030 A10 11095828 C T downstream_gene_variant MODIFIER c.*4520C>T| S270
113825 BAA10g09030 A10 11095896 C T downstream_gene_variant MODIFIER c.*4588C>T| S17