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
198651 BAA02g29860 A02 17154329 G A missense_variant MODERATE c.1292C>T|p.Thr431Ile S134
198652 BAA02g29830 A02 17154549 C T upstream_gene_variant MODIFIER c.-4436G>A| S15
S156
S3
S34
198653 BAA02g29860 A02 17157130 C T synonymous_variant LOW c.165G>A|p.Gln55Gln S138
198654 BAA02g29840 A02 17157446 G A upstream_gene_variant MODIFIER c.-4901C>T| S278
198655 BAA02g29860 A02 17158041 G A upstream_gene_variant MODIFIER c.-623C>T| S281
198656 BAA02g29860-BAA02g29870 A02 17163918 G A intergenic_region MODIFIER n.17163918G>A| S33
198657 BAA02g29860-BAA02g29870 A02 17164189 G A intergenic_region MODIFIER n.17164189G>A| S70
198658 BAA02g29860-BAA02g29870 A02 17164487 C T intergenic_region MODIFIER n.17164487C>T| S162
198659 BAA02g29860-BAA02g29870 A02 17164739 G A intergenic_region MODIFIER n.17164739G>A| S197
198660 BAA02g29860-BAA02g29870 A02 17164884 G A intergenic_region MODIFIER n.17164884G>A| S191
198661 BAA02g29860-BAA02g29870 A02 17165071 G A intergenic_region MODIFIER n.17165071G>A| S69
198662 BAA02g29870 A02 17167046 G A upstream_gene_variant MODIFIER c.-3921G>A| S166
198663 BAA02g29870 A02 17168527 G A upstream_gene_variant MODIFIER c.-2440G>A| S259
198664 BAA02g29870 A02 17168530 C T upstream_gene_variant MODIFIER c.-2437C>T| S2
198665 BAA02g29870 A02 17169144 G A upstream_gene_variant MODIFIER c.-1823G>A| S229
198666 BAA02g29870 A02 17169225 C T upstream_gene_variant MODIFIER c.-1742C>T| S171
198667 BAA02g29870 A02 17169254 C T upstream_gene_variant MODIFIER c.-1713C>T| S9
198668 BAA02g29870 A02 17169679 C T upstream_gene_variant MODIFIER c.-1288C>T| S112
198669 BAA02g29870 A02 17170084 G A upstream_gene_variant MODIFIER c.-883G>A| S210
198670 BAA02g29870 A02 17170905 C T upstream_gene_variant MODIFIER c.-62C>T| S103
198671 BAA02g29870 A02 17170929 C T upstream_gene_variant MODIFIER c.-38C>T| S239
198672 BAA02g29870 A02 17171330 C T stop_gained HIGH c.364C>T|p.Gln122* S139
198673 BAA02g29870 A02 17171805 C T intron_variant MODIFIER c.670+169C>T| S130
198674 BAA02g29870 A02 17172034 G A intron_variant MODIFIER c.670+398G>A| S278
198675 BAA02g29870 A02 17172217 G A intron_variant MODIFIER c.671-361G>A| S132
S137
S215
S89