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
188101 BAA02g24870 A02 13585696 C T upstream_gene_variant MODIFIER c.-3828G>A| S114
188102 BAA02g24870 A02 13585868 G A upstream_gene_variant MODIFIER c.-4000C>T| S201
188103 BAA02g24870 A02 13585959 C T upstream_gene_variant MODIFIER c.-4091G>A| S65
188104 BAA02g24870 A02 13586408 G A upstream_gene_variant MODIFIER c.-4540C>T| S146
188105 BAA02g24880 A02 13588017 C T upstream_gene_variant MODIFIER c.-2157C>T| S42
188106 BAA02g24880 A02 13588481 G A upstream_gene_variant MODIFIER c.-1693G>A| S288
188107 BAA02g24880 A02 13589136 C T upstream_gene_variant MODIFIER c.-1038C>T| S277
188108 BAA02g24880 A02 13589531 C T upstream_gene_variant MODIFIER c.-643C>T| S233
188109 BAA02g24880 A02 13590161 G A upstream_gene_variant MODIFIER c.-13G>A| S20
188110 BAA02g24880 A02 13590215 G A missense_variant MODERATE c.42G>A|p.Met14Ile S246
188111 BAA02g24880 A02 13590513 G A downstream_gene_variant MODIFIER c.*13G>A| S5
188112 BAA02g24880 A02 13592854 G A downstream_gene_variant MODIFIER c.*2354G>A| S278
188113 BAA02g24880 A02 13594168 G A downstream_gene_variant MODIFIER c.*3668G>A| S155
188114 BAA02g24880 A02 13594301 G A downstream_gene_variant MODIFIER c.*3801G>A| S96
188115 BAA02g24890 A02 13595586 G A downstream_gene_variant MODIFIER c.*426C>T| S184
188116 BAA02g24890 A02 13595706 G A downstream_gene_variant MODIFIER c.*306C>T| S11
188117 BAA02g24890 A02 13596256 G A missense_variant MODERATE c.979C>T|p.Leu327Phe S80
188118 BAA02g24890 A02 13597399 C T synonymous_variant LOW c.624G>A|p.Pro208Pro S1
S90
188119 BAA02g24890 A02 13598374 C T intron_variant MODIFIER c.466-520G>A| S293
188120 BAA02g24890 A02 13598496 C T intron_variant MODIFIER c.466-642G>A| S296
188121 BAA02g24890 A02 13599532 T A intron_variant MODIFIER c.465+363A>T| S138
188122 BAA02g24890 A02 13599575 C T intron_variant MODIFIER c.465+320G>A| S282
188123 BAA02g24890 A02 13600298 C T missense_variant MODERATE c.346G>A|p.Glu116Lys S32
188124 BAA02g24890 A02 13601004 G A intron_variant MODIFIER c.176-536C>T| S150
188125 BAA02g24890 A02 13601241 C T intron_variant MODIFIER c.176-773G>A| S88