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
195651 BAA02g28630 A02 16108377 C T downstream_gene_variant MODIFIER c.*2264C>T| S275
195652 BAA02g28630 A02 16109057 C T downstream_gene_variant MODIFIER c.*2944C>T| S11
195653 BAA02g28630 A02 16109176 G A downstream_gene_variant MODIFIER c.*3063G>A| S225
195654 BAA02g28630 A02 16110460 C T downstream_gene_variant MODIFIER c.*4347C>T| S176
195655 BAA02g28630 A02 16110570 C T downstream_gene_variant MODIFIER c.*4457C>T| S87
195656 BAA02g28630 A02 16110788 C T downstream_gene_variant MODIFIER c.*4675C>T| S39
195657 BAA02g28640 A02 16111155 C T downstream_gene_variant MODIFIER c.*2126G>A| S255
195658 BAA02g28650 A02 16112487 G A upstream_gene_variant MODIFIER c.-3964G>A| S188
195659 BAA02g28640 A02 16113990 C T upstream_gene_variant MODIFIER c.-320G>A| S183
S198
195660 BAA02g28640 A02 16115192 C T upstream_gene_variant MODIFIER c.-1522G>A| S293
195661 BAA02g28650 A02 16117083 G A synonymous_variant LOW c.633G>A|p.Arg211Arg S184
195662 BAA02g28650 A02 16119384 C T intron_variant MODIFIER c.658-240C>T| S42
195663 BAA02g28650 A02 16119710 G A synonymous_variant LOW c.744G>A|p.Gln248Gln S280
195664 BAA02g28650 A02 16120334 C T missense_variant MODERATE c.1196C>T|p.Pro399Leu S88
195665 BAA02g28650 A02 16120769 C T intron_variant MODIFIER c.1566-23C>T| S231
195666 BAA02g28650 A02 16120901 G A missense_variant MODERATE c.1675G>A|p.Asp559Asn S294
195667 BAA02g28650 A02 16121089 G A synonymous_variant LOW c.1863G>A|p.Gln621Gln S204
195668 BAA02g28650 A02 16121548 G A downstream_gene_variant MODIFIER c.*456G>A| S188
195669 BAA02g28650 A02 16121887 C T downstream_gene_variant MODIFIER c.*795C>T| S277
195670 BAA02g28650 A02 16121947 C T downstream_gene_variant MODIFIER c.*855C>T| S255
195671 BAA02g28650 A02 16122195 G A downstream_gene_variant MODIFIER c.*1103G>A| S306
195672 BAA02g28650 A02 16122241 G A downstream_gene_variant MODIFIER c.*1149G>A| S136
195673 BAA02g28650 A02 16122265 G A downstream_gene_variant MODIFIER c.*1173G>A| S245
195674 BAA02g28650 A02 16123487 C T downstream_gene_variant MODIFIER c.*2395C>T| S66
195675 BAA02g28650 A02 16123513 G A downstream_gene_variant MODIFIER c.*2421G>A| S298