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
180801 BAA02g20530 A02 10895259 G A missense_variant MODERATE c.266C>T|p.Ala89Val S256
180802 BAA02g20530 A02 10895794 C T upstream_gene_variant MODIFIER c.-270G>A| S277
180803 BAA02g20530 A02 10896509 C T upstream_gene_variant MODIFIER c.-985G>A| S219
S72
180804 BAA02g20530 A02 10896539 C T upstream_gene_variant MODIFIER c.-1015G>A| S250
180805 BAA02g20530 A02 10896841 G A upstream_gene_variant MODIFIER c.-1317C>T| S69
180806 BAA02g20530 A02 10897385 C T upstream_gene_variant MODIFIER c.-1861G>A| S179
180807 BAA02g20530 A02 10897550 C T upstream_gene_variant MODIFIER c.-2026G>A| S209
180808 BAA02g20530 A02 10898083 G A upstream_gene_variant MODIFIER c.-2559C>T| S256
180809 BAA02g20530 A02 10898781 G A upstream_gene_variant MODIFIER c.-3257C>T| S173
180810 BAA02g20530 A02 10898985 C T upstream_gene_variant MODIFIER c.-3461G>A| S212
180811 BAA02g20530 A02 10899606 C T upstream_gene_variant MODIFIER c.-4082G>A| S25
180812 BAA02g20530 A02 10899984 C A upstream_gene_variant MODIFIER c.-4460G>T| S64
180813 BAA02g20540 A02 10900148 C T missense_variant MODERATE c.1046G>A|p.Ser349Asn S189
180814 BAA02g20540 A02 10900326 C T missense_variant MODERATE c.868G>A|p.Glu290Lys S202
180815 BAA02g20540 A02 10900691 C T missense_variant MODERATE c.503G>A|p.Arg168Lys S9
180816 BAA02g20540 A02 10902002 C T upstream_gene_variant MODIFIER c.-809G>A| S149
180817 BAA02g20540 A02 10902496 C T upstream_gene_variant MODIFIER c.-1303G>A| S262
180818 BAA02g20540 A02 10902864 C T upstream_gene_variant MODIFIER c.-1671G>A| S2
180819 BAA02g20540 A02 10905567 C T upstream_gene_variant MODIFIER c.-4374G>A| S120
180820 BAA02g20550 A02 10906594 G A upstream_gene_variant MODIFIER c.-1027G>A| S173
180821 BAA02g20560 A02 10909106 C T upstream_gene_variant MODIFIER c.-364C>T| S152
180822 BAA02g20560 A02 10909518 C T missense_variant MODERATE c.49C>T|p.Pro17Ser S260
180823 BAA02g20560 A02 10909561 C T missense_variant MODERATE c.92C>T|p.Pro31Leu S189
180824 BAA02g20560 A02 10910653 C T stop_gained HIGH c.634C>T|p.Arg212* S80
180825 BAA02g20550 A02 10911181 C T downstream_gene_variant MODIFIER c.*3041C>T| S9