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


Gene ID

Results: 1 - 28 of 28 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g26890 A05 31407019 T A upstream_gene_variant MODIFIER c.-4590T>A| S292
2 BAA05g26890 A05 31407542 G A upstream_gene_variant MODIFIER c.-4067G>A| S76
3 BAA05g26890 A05 31408074 G T upstream_gene_variant MODIFIER c.-3535G>T| S64
4 BAA05g26890 A05 31408109 C T upstream_gene_variant MODIFIER c.-3500C>T| S41
5 BAA05g26890 A05 31408891 C T upstream_gene_variant MODIFIER c.-2718C>T| S230
6 BAA05g26890 A05 31409919 G A upstream_gene_variant MODIFIER c.-1690G>A| S283
7 BAA05g26890 A05 31410972 G A upstream_gene_variant MODIFIER c.-637G>A| S75
S81
8 BAA05g26890 A05 31411050 C T upstream_gene_variant MODIFIER c.-559C>T| S278
9 BAA05g26890 A05 31411100 G A upstream_gene_variant MODIFIER c.-509G>A| S188
10 BAA05g26890 A05 31411267 G A upstream_gene_variant MODIFIER c.-342G>A| S11
11 BAA05g26890 A05 31411302 G A upstream_gene_variant MODIFIER c.-307G>A| S134
12 BAA05g26890 A05 31411400 G A upstream_gene_variant MODIFIER c.-209G>A| S173
13 BAA05g26890 A05 31411887 C T synonymous_variant LOW c.279C>T|p.His93His S290
14 BAA05g26890 A05 31412027 C T missense_variant MODERATE c.419C>T|p.Thr140Ile S288
15 BAA05g26890 A05 31412072 C T missense_variant MODERATE c.464C>T|p.Thr155Ile S123
16 BAA05g26890 A05 31413516 G A downstream_gene_variant MODIFIER c.*660G>A| S284
17 BAA05g26890 A05 31413610 C T downstream_gene_variant MODIFIER c.*754C>T| S81
S85
18 BAA05g26890 A05 31413915 C T downstream_gene_variant MODIFIER c.*1059C>T| S69
19 BAA05g26890 A05 31413980 G A downstream_gene_variant MODIFIER c.*1124G>A| S211
20 BAA05g26890 A05 31415005 G A downstream_gene_variant MODIFIER c.*2149G>A| S124
21 BAA05g26890 A05 31415760 G A downstream_gene_variant MODIFIER c.*2904G>A| S97
22 BAA05g26890 A05 31416203 A G downstream_gene_variant MODIFIER c.*3347A>G| S277
23 BAA05g26890 A05 31416230 C T downstream_gene_variant MODIFIER c.*3374C>T| S221
24 BAA05g26890 A05 31416267 C T downstream_gene_variant MODIFIER c.*3411C>T| S81
25 BAA05g26890 A05 31416788 C T downstream_gene_variant MODIFIER c.*3932C>T| S89