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
165101 BAA02g11350 A02 5131380 G A upstream_gene_variant MODIFIER c.-1223C>T| S143
165102 BAA02g11350 A02 5131700 C T upstream_gene_variant MODIFIER c.-1543G>A| S208
S219
165103 BAA02g11350 A02 5131755 C T upstream_gene_variant MODIFIER c.-1598G>A| S77
S82
165104 BAA02g11350 A02 5132479 C T upstream_gene_variant MODIFIER c.-2322G>A| S267
165105 BAA02g11350 A02 5133109 G A upstream_gene_variant MODIFIER c.-2952C>T| S11
165106 BAA02g11370 A02 5133831 C T synonymous_variant LOW c.1500G>A|p.Lys500Lys S200
165107 BAA02g11370 A02 5134363 G A missense_variant MODERATE c.968C>T|p.Thr323Met S308
165108 BAA02g11370 A02 5135803 G A upstream_gene_variant MODIFIER c.-232C>T| S69
165109 BAA02g11370 A02 5136151 C T upstream_gene_variant MODIFIER c.-580G>A| S32
165110 BAA02g11370 A02 5136415 C T upstream_gene_variant MODIFIER c.-844G>A| S301
S304
165111 BAA02g11370 A02 5137757 A G upstream_gene_variant MODIFIER c.-2186T>C| S221
165112 BAA02g11370 A02 5139127 G A upstream_gene_variant MODIFIER c.-3556C>T| S208
S93
165113 BAA02g11380 A02 5142090 G A synonymous_variant LOW c.1227C>T|p.His409His S303
165114 BAA02g11380 A02 5142438 C T synonymous_variant LOW c.879G>A|p.Arg293Arg S278
165115 BAA02g11380 A02 5142593 G A intron_variant MODIFIER c.772-48C>T| S287
165116 BAA02g11380 A02 5142831 C T intron_variant MODIFIER c.772-286G>A| S200
165117 BAA02g11380 A02 5143277 C T missense_variant MODERATE c.625G>A|p.Asp209Asn S171
165118 BAA02g11380 A02 5146143 G A upstream_gene_variant MODIFIER c.-1797C>T| S122
165119 BAA02g11380 A02 5147953 G A upstream_gene_variant MODIFIER c.-3607C>T| S247
165120 BAA02g11380 A02 5148766 C T upstream_gene_variant MODIFIER c.-4420G>A| S267
165121 BAA02g11380-BAA02g11390 A02 5150499 C T intergenic_region MODIFIER n.5150499C>T| S218
165122 BAA02g11380-BAA02g11390 A02 5150539 G A intergenic_region MODIFIER n.5150539G>A| S290
165123 BAA02g11380-BAA02g11390 A02 5153937 C T intergenic_region MODIFIER n.5153937C>T| S13
165124 BAA02g11380-BAA02g11390 A02 5153995 C T intergenic_region MODIFIER n.5153995C>T| S209
165125 BAA02g11390 A02 5159168 G A upstream_gene_variant MODIFIER c.-2202G>A| S298