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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g46810 A02 37931677 C T upstream_gene_variant MODIFIER c.-4382C>T| S250
2 BAA02g46810 A02 37932126 G A upstream_gene_variant MODIFIER c.-3933G>A| S84
S93
3 BAA02g46810 A02 37932191 G A upstream_gene_variant MODIFIER c.-3868G>A| S264
4 BAA02g46810 A02 37933110 G A upstream_gene_variant MODIFIER c.-2949G>A| S71
5 BAA02g46810 A02 37933722 C T upstream_gene_variant MODIFIER c.-2337C>T| S299
6 BAA02g46810 A02 37933874 G A upstream_gene_variant MODIFIER c.-2185G>A| S282
7 BAA02g46810 A02 37934374 C T upstream_gene_variant MODIFIER c.-1685C>T| S165
S211
S227
8 BAA02g46810 A02 37935442 C T upstream_gene_variant MODIFIER c.-617C>T| S172
S217
9 BAA02g46810 A02 37936093 C T missense_variant MODERATE c.35C>T|p.Thr12Ile S273
10 BAA02g46810 A02 37936364 C T synonymous_variant LOW c.306C>T|p.Val102Val S138
11 BAA02g46810 A02 37936395 C T missense_variant MODERATE c.337C>T|p.Leu113Phe S262
12 BAA02g46810 A02 37936405 C T missense_variant MODERATE c.347C>T|p.Ser116Phe S234
13 BAA02g46810 A02 37936451 C T synonymous_variant LOW c.393C>T|p.Gly131Gly S181
14 BAA02g46810 A02 37937851 T G downstream_gene_variant MODIFIER c.*878T>G| S11
15 BAA02g46810 A02 37938448 C A downstream_gene_variant MODIFIER c.*1475C>A| S184
16 BAA02g46810 A02 37938716 C T downstream_gene_variant MODIFIER c.*1743C>T| S283
17 BAA02g46810 A02 37938737 C T downstream_gene_variant MODIFIER c.*1764C>T| S299
18 BAA02g46810 A02 37938940 C T downstream_gene_variant MODIFIER c.*1967C>T| S129
19 BAA02g46810 A02 37939407 C T downstream_gene_variant MODIFIER c.*2434C>T| S191
20 BAA02g46810 A02 37940717 T C downstream_gene_variant MODIFIER c.*3744T>C| S115
21 BAA02g46810 A02 37941048 C T downstream_gene_variant MODIFIER c.*4075C>T| S116
22 BAA02g46810 A02 37941511 C T downstream_gene_variant MODIFIER c.*4538C>T| S208
S93
23 BAA02g46810 A02 37941730 C T downstream_gene_variant MODIFIER c.*4757C>T| S202