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
151101 BAA10g34990 A10 24438304 C T upstream_gene_variant MODIFIER c.-1587G>A| S192
151102 BAA10g34990 A10 24438499 G A upstream_gene_variant MODIFIER c.-1782C>T| S62
151103 BAA10g34990 A10 24438528 G A upstream_gene_variant MODIFIER c.-1811C>T| S179
151104 BAA10g34990 A10 24438881 G A upstream_gene_variant MODIFIER c.-2164C>T| S111
151105 BAA10g34990 A10 24438893 G A upstream_gene_variant MODIFIER c.-2176C>T| S203
151106 BAA10g35010 A10 24444901 C T downstream_gene_variant MODIFIER c.*15C>T| S72
S78
151107 BAA10g35020 A10 24445829 C T upstream_gene_variant MODIFIER c.-302G>A| S19
151108 BAA10g35020 A10 24446467 C T upstream_gene_variant MODIFIER c.-940G>A| S40
S49
151109 BAA10g35020 A10 24447028 G A upstream_gene_variant MODIFIER c.-1501C>T| S280
151110 BAA10g35020 A10 24447458 G A upstream_gene_variant MODIFIER c.-1931C>T| S162
151111 BAA10g35020 A10 24447781 G A upstream_gene_variant MODIFIER c.-2254C>T| S63
151112 CHR_START-BAA02g00010 A02 1957 G A intergenic_region MODIFIER n.1957G>A| S296
151113 CHR_START-BAA02g00010 A02 2623 G A intergenic_region MODIFIER n.2623G>A| S149
151114 CHR_START-BAA02g00010 A02 2656 C T intergenic_region MODIFIER n.2656C>T| S152
151115 BAA02g00010 A02 7511 C T upstream_gene_variant MODIFIER c.-429C>T| S6
151116 BAA02g00010 A02 8006 C T missense_variant MODERATE c.67C>T|p.Pro23Ser S201
151117 BAA02g00010 A02 8706 G A missense_variant MODERATE c.527G>A|p.Gly176Glu S118
151118 BAA02g00010 A02 8708 G A missense_variant MODERATE c.529G>A|p.Gly177Arg S7
151119 BAA02g00010 A02 9120 C T intron_variant MODIFIER c.699-14C>T| S138
151120 BAA02g00010 A02 9662 C T intron_variant MODIFIER c.896+169C>T| S124
151121 BAA02g00010 A02 10951 G A intron_variant MODIFIER c.1087-594G>A| S10
151122 BAA02g00010 A02 11271 C T intron_variant MODIFIER c.1087-274C>T| S111
151123 BAA02g00010 A02 11916 C T intron_variant MODIFIER c.1171-40C>T| S306
151124 BAA02g00010 A02 12001 G A missense_variant MODERATE c.1216G>A|p.Asp406Asn S215
151125 BAA02g00020 A02 14339 G A upstream_gene_variant MODIFIER c.-3429G>A| S149