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
102651 BAA10g07520-BAA10g07530 A10 4444601 C T intergenic_region MODIFIER n.4444601C>T| S210
S225
102652 BAA10g07520-BAA10g07530 A10 4444609 C T intergenic_region MODIFIER n.4444609C>T| S244
102653 BAA10g07520-BAA10g07530 A10 4444670 C T intergenic_region MODIFIER n.4444670C>T| S98
102654 BAA10g07520-BAA10g07530 A10 4444819 C T intergenic_region MODIFIER n.4444819C>T| S157
102655 BAA10g07520-BAA10g07530 A10 4445026 C T intergenic_region MODIFIER n.4445026C>T| S185
102656 BAA10g07520-BAA10g07530 A10 4445432 G A intergenic_region MODIFIER n.4445432G>A| S62
102657 BAA10g07520-BAA10g07530 A10 4446096 G A intergenic_region MODIFIER n.4446096G>A| S186
102658 BAA10g07520-BAA10g07530 A10 4446508 G A intergenic_region MODIFIER n.4446508G>A| S286
102659 BAA10g07520-BAA10g07530 A10 4446539 G A intergenic_region MODIFIER n.4446539G>A| S20
102660 BAA10g07520-BAA10g07530 A10 4446887 G A intergenic_region MODIFIER n.4446887G>A| S157
S166
S167
S236
S262
102661 BAA10g07530 A10 4447527 C T downstream_gene_variant MODIFIER c.*4423G>A| S275
102662 BAA10g07530 A10 4448039 G A downstream_gene_variant MODIFIER c.*3911C>T| S68
102663 BAA10g07530 A10 4449354 C T downstream_gene_variant MODIFIER c.*2596G>A| S235
102664 BAA10g07530 A10 4449788 G A downstream_gene_variant MODIFIER c.*2162C>T| S138
102665 BAA10g07530 A10 4450793 G A downstream_gene_variant MODIFIER c.*1157C>T| S230
102666 BAA10g07530 A10 4451465 G A downstream_gene_variant MODIFIER c.*485C>T| S13
102667 BAA10g07530 A10 4451526 G A downstream_gene_variant MODIFIER c.*424C>T| S241
102668 BAA10g07530 A10 4452506 G A missense_variant MODERATE c.68C>T|p.Ser23Leu S16
102669 BAA10g07530 A10 4453010 C T upstream_gene_variant MODIFIER c.-437G>A| S124
102670 BAA10g07530 A10 4453258 C T upstream_gene_variant MODIFIER c.-685G>A| S19
102671 BAA10g07530 A10 4453807 G A upstream_gene_variant MODIFIER c.-1234C>T| S13
102672 BAA10g07530 A10 4455028 C T upstream_gene_variant MODIFIER c.-2455G>A| S143
102673 BAA10g07530 A10 4456189 G A upstream_gene_variant MODIFIER c.-3616C>T| S306
S308
102674 BAA10g07530 A10 4456434 C T upstream_gene_variant MODIFIER c.-3861G>A| S23
102675 BAA10g07530-BAA10g07540 A10 4466853 C T intergenic_region MODIFIER n.4466853C>T| S144