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
203701 BAA02g31540-BAA02g31550 A02 18984989 C T intergenic_region MODIFIER n.18984989C>T| S175
203702 BAA02g31540-BAA02g31550 A02 18985166 G A intergenic_region MODIFIER n.18985166G>A| S187
203703 BAA02g31540-BAA02g31550 A02 18985966 C T intergenic_region MODIFIER n.18985966C>T| S206
203704 BAA02g31540-BAA02g31550 A02 18986883 C T intergenic_region MODIFIER n.18986883C>T| S135
203705 BAA02g31540-BAA02g31550 A02 18987830 G A intergenic_region MODIFIER n.18987830G>A| S275
203706 BAA02g31540-BAA02g31550 A02 18988269 G A intergenic_region MODIFIER n.18988269G>A| S155
203707 BAA02g31550 A02 18989850 C T upstream_gene_variant MODIFIER c.-3772C>T| S49
203708 BAA02g31550 A02 18993126 C T upstream_gene_variant MODIFIER c.-496C>T| S163
203709 BAA02g31550 A02 18994095 G A missense_variant MODERATE c.356G>A|p.Arg119Lys S246
203710 BAA02g31550 A02 18994474 G A missense_variant MODERATE c.402G>A|p.Met134Ile S197
203711 BAA02g31550 A02 18994492 G A synonymous_variant LOW c.420G>A|p.Lys140Lys S110
203712 BAA02g31550 A02 18994767 C T missense_variant MODERATE c.695C>T|p.Ala232Val S139
203713 BAA02g31560 A02 18995007 G A upstream_gene_variant MODIFIER c.-65G>A| S86
203714 BAA02g31560 A02 18995048 G A upstream_gene_variant MODIFIER c.-24G>A| S259
203715 BAA02g31550 A02 18995990 C T downstream_gene_variant MODIFIER c.*1105C>T| S1
S90
203716 BAA02g31550 A02 18996579 C T downstream_gene_variant MODIFIER c.*1694C>T| S284
203717 BAA02g31560 A02 18997256 G A missense_variant MODERATE c.863G>A|p.Arg288Lys S98
203718 BAA02g31550 A02 18997526 C T downstream_gene_variant MODIFIER c.*2641C>T| S135
203719 BAA02g31550 A02 18997797 C T downstream_gene_variant MODIFIER c.*2912C>T| S255
203720 BAA02g31550 A02 18998139 G T downstream_gene_variant MODIFIER c.*3254G>T| S96
203721 BAA02g31550 A02 18999071 C T downstream_gene_variant MODIFIER c.*4186C>T| S224
203722 BAA02g31550 A02 18999150 C T downstream_gene_variant MODIFIER c.*4265C>T| S301
S304
203723 BAA02g31550 A02 18999335 C T downstream_gene_variant MODIFIER c.*4450C>T| S205
S240
203724 BAA02g31560 A02 19001336 C T downstream_gene_variant MODIFIER c.*4073C>T| S165
S211
S227
203725 BAA02g31560-BAA02g31570 A02 19002460 G A intergenic_region MODIFIER n.19002460G>A| S146