Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g47030 A02 38046850 G A upstream_gene_variant MODIFIER c.-3518G>A| S60
2 BAA02g47030 A02 38047512 C T upstream_gene_variant MODIFIER c.-2856C>T| S122
3 BAA02g47030 A02 38047717 C T upstream_gene_variant MODIFIER c.-2651C>T| S182
4 BAA02g47030 A02 38047894 C T upstream_gene_variant MODIFIER c.-2474C>T| S140
5 BAA02g47030 A02 38047949 C T upstream_gene_variant MODIFIER c.-2419C>T| S202
6 BAA02g47030 A02 38048046 G A upstream_gene_variant MODIFIER c.-2322G>A| S288
7 BAA02g47030 A02 38048144 G A upstream_gene_variant MODIFIER c.-2224G>A| S259
8 BAA02g47030 A02 38048206 C T upstream_gene_variant MODIFIER c.-2162C>T| S205
9 BAA02g47030 A02 38048370 C T upstream_gene_variant MODIFIER c.-1998C>T| S277
10 BAA02g47030 A02 38048562 G A upstream_gene_variant MODIFIER c.-1806G>A| S30
11 BAA02g47030 A02 38048716 G A upstream_gene_variant MODIFIER c.-1652G>A| S209
12 BAA02g47030 A02 38049271 G A upstream_gene_variant MODIFIER c.-1097G>A| S261
13 BAA02g47030 A02 38049593 C T upstream_gene_variant MODIFIER c.-775C>T| S17
14 BAA02g47030 A02 38049787 C T upstream_gene_variant MODIFIER c.-581C>T| S158
15 BAA02g47030 A02 38051273 G A synonymous_variant LOW c.477G>A|p.Glu159Glu S221
16 BAA02g47030 A02 38051283 G A missense_variant MODERATE c.487G>A|p.Asp163Asn S155
S211
17 BAA02g47030 A02 38052275 C T intron_variant MODIFIER c.1007+117C>T| S73
18 BAA02g47030 A02 38052375 C T intron_variant MODIFIER c.1008-196C>T| S165
19 BAA02g47030 A02 38052781 C T synonymous_variant LOW c.1218C>T|p.Phe406Phe S303
20 BAA02g47030 A02 38053215 G A synonymous_variant LOW c.1515G>A|p.Val505Val S166
21 BAA02g47030 A02 38054086 C T synonymous_variant LOW c.2242C>T|p.Leu748Leu S116
22 BAA02g47030 A02 38054172 C T intron_variant MODIFIER c.2307+21C>T| S241
23 BAA02g47030 A02 38054557 G A stop_gained HIGH c.2376G>A|p.Trp792* S60
24 BAA02g47030 A02 38054955 G A intron_variant MODIFIER c.2658+116G>A| S207
25 BAA02g47030 A02 38055513 G A missense_variant MODERATE c.2891G>A|p.Gly964Glu S36