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
151801 BAA02g00430 A02 236438 G A upstream_gene_variant MODIFIER c.-1230G>A| S17
151802 BAA02g00430 A02 236847 C T upstream_gene_variant MODIFIER c.-821C>T| S245
151803 BAA02g00430 A02 237049 G A upstream_gene_variant MODIFIER c.-619G>A| S62
151804 BAA02g00430 A02 237647 C T upstream_gene_variant MODIFIER c.-21C>T| S180
151805 BAA02g00420 A02 239368 G A downstream_gene_variant MODIFIER c.*3703G>A| S164
151806 BAA02g00440 A02 240758 C T missense_variant MODERATE c.155G>A|p.Gly52Asp S159
S187
S188
S243
S276
S299
151807 BAA02g00440 A02 241316 G A upstream_gene_variant MODIFIER c.-404C>T| S149
S289
S290
151808 BAA02g00440 A02 241398 C T upstream_gene_variant MODIFIER c.-486G>A| S55
151809 BAA02g00440 A02 242712 C T upstream_gene_variant MODIFIER c.-1800G>A| S82
S92
151810 BAA02g00440 A02 242838 G A upstream_gene_variant MODIFIER c.-1926C>T| S126
151811 BAA02g00440 A02 242854 C T upstream_gene_variant MODIFIER c.-1942G>A| S53
151812 BAA02g00440 A02 243568 C T upstream_gene_variant MODIFIER c.-2656G>A| S185
151813 BAA02g00440 A02 244645 G A upstream_gene_variant MODIFIER c.-3733C>T| S223
151814 BAA02g00440 A02 245201 C T upstream_gene_variant MODIFIER c.-4289G>A| S123
151815 BAA02g00440 A02 245852 G A upstream_gene_variant MODIFIER c.-4940C>T| S70
151816 BAA02g00450 A02 246650 G A upstream_gene_variant MODIFIER c.-2103G>A| S5
151817 BAA02g00450 A02 246869 C T upstream_gene_variant MODIFIER c.-1884C>T| S6
151818 BAA02g00450 A02 247520 G A upstream_gene_variant MODIFIER c.-1233G>A| S249
151819 BAA02g00450 A02 247543 C T upstream_gene_variant MODIFIER c.-1210C>T| S186
151820 BAA02g00450 A02 247787 G A upstream_gene_variant MODIFIER c.-966G>A| S206
S26
151821 BAA02g00450 A02 247891 G A upstream_gene_variant MODIFIER c.-862G>A| S151
S153
S257
S262
S263
151822 BAA02g00450 A02 248919 C T missense_variant MODERATE c.85C>T|p.Leu29Phe S185
151823 BAA02g00450 A02 249300 G A missense_variant MODERATE c.275G>A|p.Gly92Asp S33
151824 BAA02g00450 A02 251623 G A downstream_gene_variant MODIFIER c.*1479G>A| S25
151825 BAA02g00460 A02 251659 C T upstream_gene_variant MODIFIER c.-4986C>T| S178