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
166451 BAA02g12510 A02 5618407 G A synonymous_variant LOW c.81C>T|p.Val27Val S161
166452 BAA02g12500 A02 5619585 G A upstream_gene_variant MODIFIER c.-2913C>T| S37
166453 BAA02g12500 A02 5619964 C T upstream_gene_variant MODIFIER c.-3292G>A| S234
166454 BAA02g12530 A02 5620672 C T missense_variant MODERATE c.664C>T|p.Leu222Phe S55
166455 BAA02g12500 A02 5620927 C T upstream_gene_variant MODIFIER c.-4255G>A| S70
166456 BAA02g12500 A02 5621605 G A upstream_gene_variant MODIFIER c.-4933C>T| S17
166457 BAA02g12540 A02 5622720 C T missense_variant MODERATE c.1126G>A|p.Glu376Lys S262
166458 BAA02g12540 A02 5623334 C T missense_variant MODERATE c.512G>A|p.Arg171His S142
166459 BAA02g12540 A02 5623940 G A missense_variant MODERATE c.19C>T|p.Arg7Cys S25
166460 BAA02g12520 A02 5624099 G A upstream_gene_variant MODIFIER c.-4743C>T| S288
166461 BAA02g12540 A02 5624455 C T upstream_gene_variant MODIFIER c.-423G>A| S16
166462 BAA02g12540 A02 5625884 G A upstream_gene_variant MODIFIER c.-1852C>T| S53
166463 BAA02g12560 A02 5629164 C T missense_variant MODERATE c.266G>A|p.Gly89Glu S116
166464 BAA02g12570 A02 5632067 G A missense_variant MODERATE c.776C>T|p.Ala259Val S247
166465 BAA02g12570 A02 5632390 C T missense_variant MODERATE c.523G>A|p.Glu175Lys S135
166466 BAA02g12570 A02 5632746 C T missense_variant MODERATE c.238G>A|p.Glu80Lys S167
166467 BAA02g12570 A02 5632765 G A synonymous_variant LOW c.219C>T|p.Leu73Leu S197
166468 BAA02g12570 A02 5632923 G A missense_variant MODERATE c.61C>T|p.Pro21Ser S45
166469 BAA02g12560 A02 5633126 G A upstream_gene_variant MODIFIER c.-3697C>T| S140
166470 BAA02g12560 A02 5634134 C T upstream_gene_variant MODIFIER c.-4705G>A| S108
166471 BAA02g12560 A02 5634294 C T upstream_gene_variant MODIFIER c.-4865G>A| S163
166472 BAA02g12570 A02 5634792 G A upstream_gene_variant MODIFIER c.-1809C>T| S17
166473 BAA02g12580 A02 5635730 G A missense_variant MODERATE c.988C>T|p.Leu330Phe S298
166474 BAA02g12580 A02 5635792 C T splice_acceptor_variant&intron_variant HIGH c.927-1G>A| S289
S290
166475 BAA02g12570 A02 5636140 G A upstream_gene_variant MODIFIER c.-3157C>T| S10