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
74851 BAA01g39440 A01 26205565 C T upstream_gene_variant MODIFIER c.-72G>A| S201
74852 BAA01g39440 A01 26205821 G A upstream_gene_variant MODIFIER c.-328C>T| S1
S90
74853 BAA01g39440 A01 26207485 C T upstream_gene_variant MODIFIER c.-1992G>A| S305
74854 BAA01g39440 A01 26207878 A G upstream_gene_variant MODIFIER c.-2385T>C| S150
74855 BAA01g39440 A01 26209203 A T upstream_gene_variant MODIFIER c.-3710T>A| S25
S280
74856 BAA01g39450 A01 26213162 C T upstream_gene_variant MODIFIER c.-4058C>T| S249
74857 BAA01g39450 A01 26213504 G A upstream_gene_variant MODIFIER c.-3716G>A| S117
74858 BAA01g39450 A01 26213560 C T upstream_gene_variant MODIFIER c.-3660C>T| S118
74859 BAA01g39450 A01 26216914 C T upstream_gene_variant MODIFIER c.-306C>T| S153
74860 BAA01g39450 A01 26218686 C T missense_variant MODERATE c.640C>T|p.Leu214Phe S270
74861 BAA01g39460 A01 26221483 C T upstream_gene_variant MODIFIER c.-509C>T| S78
74862 BAA01g39460 A01 26221521 C T upstream_gene_variant MODIFIER c.-471C>T| S104
S52
74863 BAA01g39460 A01 26221904 G A upstream_gene_variant MODIFIER c.-88G>A| S113
74864 BAA01g39460 A01 26223878 G A synonymous_variant LOW c.1887G>A|p.Gly629Gly S70
74865 BAA01g39450 A01 26224270 G A downstream_gene_variant MODIFIER c.*3055G>A| S221
74866 BAA01g39450 A01 26225060 G A downstream_gene_variant MODIFIER c.*3845G>A| S187
74867 BAA01g39450 A01 26225265 G A downstream_gene_variant MODIFIER c.*4050G>A| S172
S217
74868 BAA01g39450 A01 26225408 G A downstream_gene_variant MODIFIER c.*4193G>A| S202
74869 BAA01g39450 A01 26225862 C T downstream_gene_variant MODIFIER c.*4647C>T| S4
74870 BAA01g39460 A01 26227543 A G downstream_gene_variant MODIFIER c.*3587A>G| S156
S169
74871 BAA01g39460 A01 26228753 G A downstream_gene_variant MODIFIER c.*4797G>A| S70
74872 BAA01g39460-BAA01g39470 A01 26228988 C T intergenic_region MODIFIER n.26228988C>T| S32
74873 BAA01g39460-BAA01g39470 A01 26229135 C T intergenic_region MODIFIER n.26229135C>T| S279
74874 BAA01g39460-BAA01g39470 A01 26230292 G A intergenic_region MODIFIER n.26230292G>A| S103
74875 BAA01g39460-BAA01g39470 A01 26231756 C T intergenic_region MODIFIER n.26231756C>T| S177