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
174651 BAA02g17460 A02 8691380 G A synonymous_variant LOW c.192G>A|p.Ala64Ala S48
174652 BAA02g17460 A02 8691869 C T missense_variant MODERATE c.418C>T|p.Pro140Ser S262
174653 BAA02g17460 A02 8692178 C T missense_variant MODERATE c.727C>T|p.Leu243Phe S128
174654 BAA02g17460 A02 8692302 G A missense_variant MODERATE c.851G>A|p.Gly284Glu S136
174655 BAA02g17470 A02 8693557 C T downstream_gene_variant MODIFIER c.*4382G>A| S181
174656 BAA02g17470 A02 8694886 G A downstream_gene_variant MODIFIER c.*3053C>T| S172
S217
174657 BAA02g17470 A02 8694907 C T downstream_gene_variant MODIFIER c.*3032G>A| S139
174658 BAA02g17460 A02 8697585 G A downstream_gene_variant MODIFIER c.*15G>A| S37
174659 BAA02g17470 A02 8698675 C T missense_variant MODERATE c.284G>A|p.Arg95Gln S218
174660 BAA02g17470 A02 8698816 C T missense_variant MODERATE c.143G>A|p.Arg48Lys S283
174661 BAA02g17470 A02 8698984 C T upstream_gene_variant MODIFIER c.-26G>A| S124
174662 BAA02g17480 A02 8705042 C T upstream_gene_variant MODIFIER c.-1059C>T| S66
174663 BAA02g17480 A02 8705287 G A upstream_gene_variant MODIFIER c.-814G>A| S298
174664 BAA02g17480 A02 8705322 G A upstream_gene_variant MODIFIER c.-779G>A| S47
174665 BAA02g17480 A02 8706169 C T synonymous_variant LOW c.69C>T|p.Leu23Leu S8
174666 BAA02g17480 A02 8706932 C T synonymous_variant LOW c.546C>T|p.Ser182Ser S38
174667 BAA02g17490 A02 8707286 G A upstream_gene_variant MODIFIER c.-4842G>A| S132
S137
S138
S215
S237
S288
S89
174668 BAA02g17490 A02 8708149 G A upstream_gene_variant MODIFIER c.-3979G>A| S98
174669 BAA02g17490 A02 8709422 C T upstream_gene_variant MODIFIER c.-2706C>T| S219
174670 BAA02g17490 A02 8711281 G A upstream_gene_variant MODIFIER c.-847G>A| S197
174671 BAA02g17490 A02 8711284 G A upstream_gene_variant MODIFIER c.-844G>A| S59
174672 BAA02g17490 A02 8713106 C T synonymous_variant LOW c.567C>T|p.Leu189Leu S293
174673 BAA02g17490 A02 8713375 C T missense_variant MODERATE c.767C>T|p.Ala256Val S87
174674 BAA02g17490 A02 8713610 G A missense_variant MODERATE c.929G>A|p.Gly310Asp S95
174675 BAA02g17490 A02 8714131 C T synonymous_variant LOW c.1377C>T|p.Ile459Ile S156
S34