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
140801 BAA10g25900 A10 20734052 G A upstream_gene_variant MODIFIER c.-1987G>A| S205
140802 BAA10g25900 A10 20734799 C T upstream_gene_variant MODIFIER c.-1240C>T| S142
140803 BAA10g25900 A10 20735912 C T upstream_gene_variant MODIFIER c.-127C>T| S294
140804 BAA10g25900 A10 20736433 G A missense_variant MODERATE c.395G>A|p.Gly132Asp S32
140805 BAA10g25910 A10 20738494 C T upstream_gene_variant MODIFIER c.-51G>A| S92
140806 BAA10g25910 A10 20739365 C T upstream_gene_variant MODIFIER c.-922G>A| S44
140807 BAA10g25920 A10 20739761 G A synonymous_variant LOW c.54G>A|p.Lys18Lys S264
140808 BAA10g25940 A10 20743498 C T upstream_gene_variant MODIFIER c.-1816C>T| S155
S211
140809 BAA10g25950 A10 20746163 G A upstream_gene_variant MODIFIER c.-1146G>A| S122
140810 BAA10g25940 A10 20746624 G A missense_variant MODERATE c.640G>A|p.Glu214Lys S33
140811 BAA10g25950 A10 20747134 C T upstream_gene_variant MODIFIER c.-175C>T| S18
140812 BAA10g25950 A10 20747163 G A upstream_gene_variant MODIFIER c.-146G>A| S69
140813 BAA10g25950 A10 20747468 C T missense_variant MODERATE c.160C>T|p.Arg54Trp S88
140814 BAA10g25960 A10 20747693 G A upstream_gene_variant MODIFIER c.-1698G>A| S67
140815 BAA10g25950 A10 20748053 C T synonymous_variant LOW c.417C>T|p.Ser139Ser S176
140816 BAA10g25950 A10 20748115 G A missense_variant MODERATE c.479G>A|p.Gly160Glu S70
140817 BAA10g25960 A10 20748711 C T upstream_gene_variant MODIFIER c.-680C>T| S140
140818 BAA10g25960 A10 20749359 C T upstream_gene_variant MODIFIER c.-32C>T| S292
140819 BAA10g25960 A10 20751459 G A synonymous_variant LOW c.1290G>A|p.Lys430Lys S70
140820 BAA10g25970 A10 20752592 C T missense_variant MODERATE c.2809G>A|p.Glu937Lys S246
140821 BAA10g25950 A10 20753443 C T downstream_gene_variant MODIFIER c.*4988C>T| S13
140822 BAA10g25970 A10 20753863 G A missense_variant MODERATE c.1933C>T|p.Pro645Ser S172
S217
140823 BAA10g25970 A10 20755534 G A synonymous_variant LOW c.591C>T|p.Ala197Ala S293
140824 BAA10g25970 A10 20755733 G A missense_variant MODERATE c.392C>T|p.Ser131Phe S280
140825 BAA10g25970 A10 20755771 C T stop_gained HIGH c.354G>A|p.Trp118* S38