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
184701 BAA02g22720 A02 12318560 G A missense_variant MODERATE c.1054G>A|p.Asp352Asn S231
184702 BAA02g22740 A02 12321587 G A upstream_gene_variant MODIFIER c.-2095G>A| S187
S20
184703 BAA02g22730 A02 12321609 C T splice_region_variant&intron_variant LOW c.817+8G>A| S179
184704 BAA02g22730 A02 12322347 G A synonymous_variant LOW c.240C>T|p.Val80Val S169
184705 BAA02g22740 A02 12322852 C T upstream_gene_variant MODIFIER c.-830C>T| S195
184706 BAA02g22730 A02 12322972 C T synonymous_variant LOW c.132G>A|p.Lys44Lys S262
184707 BAA02g22730 A02 12323609 C T upstream_gene_variant MODIFIER c.-506G>A| S242
184708 BAA02g22730 A02 12324324 C T upstream_gene_variant MODIFIER c.-1221G>A| S56
184709 BAA02g22730 A02 12325376 C T upstream_gene_variant MODIFIER c.-2273G>A| S16
184710 BAA02g22740 A02 12326112 C T stop_gained HIGH c.1174C>T|p.Gln392* S262
184711 BAA02g22740 A02 12326429 C T synonymous_variant LOW c.1491C>T|p.Phe497Phe S226
184712 BAA02g22740 A02 12327319 G A missense_variant MODERATE c.2089G>A|p.Glu697Lys S70
184713 BAA02g22740 A02 12328343 C T missense_variant MODERATE c.2648C>T|p.Ser883Phe S116
184714 BAA02g22740 A02 12328928 G A missense_variant MODERATE c.3233G>A|p.Gly1078Asp S99
184715 BAA02g22760 A02 12331283 C T upstream_gene_variant MODIFIER c.-2907C>T| S246
184716 BAA02g22760 A02 12332062 C T upstream_gene_variant MODIFIER c.-2128C>T| S240
184717 BAA02g22750 A02 12332839 G A upstream_gene_variant MODIFIER c.-33C>T| S92
184718 BAA02g22750 A02 12332849 G A upstream_gene_variant MODIFIER c.-43C>T| S61
184719 BAA02g22750 A02 12332951 G A upstream_gene_variant MODIFIER c.-145C>T| S303
184720 BAA02g22750 A02 12335120 G A upstream_gene_variant MODIFIER c.-2314C>T| S274
184721 BAA02g22750 A02 12336004 C T upstream_gene_variant MODIFIER c.-3198G>A| S250
184722 BAA02g22750 A02 12336524 G A upstream_gene_variant MODIFIER c.-3718C>T| S60
184723 BAA02g22750 A02 12336788 G A upstream_gene_variant MODIFIER c.-3982C>T| S202
184724 BAA02g22750 A02 12336815 C T upstream_gene_variant MODIFIER c.-4009G>A| S283
184725 BAA02g22750 A02 12337052 C T upstream_gene_variant MODIFIER c.-4246G>A| S159
S188
S243
S276
S298
S299