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
132101 BAA10g19110 A10 17651443 C T upstream_gene_variant MODIFIER c.-2326C>T| S81
S85
132102 BAA10g19110 A10 17651614 C T upstream_gene_variant MODIFIER c.-2155C>T| S84
132103 BAA10g19110 A10 17652008 G A upstream_gene_variant MODIFIER c.-1761G>A| S184
132104 BAA10g19110 A10 17653509 C T upstream_gene_variant MODIFIER c.-260C>T| S10
132105 BAA10g19110 A10 17653645 G A upstream_gene_variant MODIFIER c.-124G>A| S198
132106 BAA10g19110 A10 17654199 G A missense_variant MODERATE c.431G>A|p.Arg144Lys S167
132107 BAA10g19110 A10 17654580 G A downstream_gene_variant MODIFIER c.*251G>A| S128
132108 BAA10g19110 A10 17655908 C T downstream_gene_variant MODIFIER c.*1579C>T| S96
132109 BAA10g19110 A10 17657287 G A downstream_gene_variant MODIFIER c.*2958G>A| S174
S27
132110 BAA10g19110 A10 17658030 G A downstream_gene_variant MODIFIER c.*3701G>A| S151
S263
132111 BAA10g19110-BAA10g19120 A10 17660314 C T intergenic_region MODIFIER n.17660314C>T| S148
S30
S31
132112 BAA10g19110-BAA10g19120 A10 17660795 G A intergenic_region MODIFIER n.17660795G>A| S279
132113 BAA10g19110-BAA10g19120 A10 17661037 G A intergenic_region MODIFIER n.17661037G>A| S265
132114 BAA10g19110-BAA10g19120 A10 17662390 C T intergenic_region MODIFIER n.17662390C>T| S26
132115 BAA10g19110-BAA10g19120 A10 17662708 C T intergenic_region MODIFIER n.17662708C>T| S119
132116 BAA10g19110-BAA10g19120 A10 17662905 G A intergenic_region MODIFIER n.17662905G>A| S236
132117 BAA10g19120 A10 17666493 G A upstream_gene_variant MODIFIER c.-1831G>A| S245
132118 BAA10g19120 A10 17666783 G A upstream_gene_variant MODIFIER c.-1541G>A| S66
132119 BAA10g19120 A10 17666952 C T upstream_gene_variant MODIFIER c.-1372C>T| S135
132120 BAA10g19120 A10 17667290 C T upstream_gene_variant MODIFIER c.-1034C>T| S237
132121 BAA10g19120 A10 17667920 C T upstream_gene_variant MODIFIER c.-404C>T| S308
132122 BAA10g19120 A10 17668480 C T missense_variant MODERATE c.157C>T|p.Pro53Ser S46
132123 BAA10g19120 A10 17669018 C T intron_variant MODIFIER c.447+45C>T| S196
132124 BAA10g19120 A10 17669230 G A synonymous_variant LOW c.609G>A|p.Ser203Ser S171
132125 BAA10g19130 A10 17670245 G A upstream_gene_variant MODIFIER c.-3775G>A| S240