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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g35060 A02 30148631 C T downstream_gene_variant MODIFIER c.*4836G>A| S107
2 BAA02g35060 A02 30148697 G A downstream_gene_variant MODIFIER c.*4770C>T| S34
3 BAA02g35060 A02 30149014 G A downstream_gene_variant MODIFIER c.*4453C>T| S204
4 BAA02g35060 A02 30149533 C T downstream_gene_variant MODIFIER c.*3934G>A| S296
5 BAA02g35060 A02 30149561 C T downstream_gene_variant MODIFIER c.*3906G>A| S118
6 BAA02g35060 A02 30150005 C T downstream_gene_variant MODIFIER c.*3462G>A| S202
7 BAA02g35060 A02 30150074 C T downstream_gene_variant MODIFIER c.*3393G>A| S271
8 BAA02g35060 A02 30150473 C T downstream_gene_variant MODIFIER c.*2994G>A| S301
S304
9 BAA02g35060 A02 30151130 G A downstream_gene_variant MODIFIER c.*2337C>T| S43
10 BAA02g35060 A02 30151390 C T downstream_gene_variant MODIFIER c.*2077G>A| S295
11 BAA02g35060 A02 30151977 C T downstream_gene_variant MODIFIER c.*1490G>A| S32
12 BAA02g35060 A02 30152118 G A downstream_gene_variant MODIFIER c.*1349C>T| S28
13 BAA02g35060 A02 30152257 G A downstream_gene_variant MODIFIER c.*1210C>T| S28
14 BAA02g35060 A02 30152260 C T downstream_gene_variant MODIFIER c.*1207G>A| S296
15 BAA02g35060 A02 30152274 C T downstream_gene_variant MODIFIER c.*1193G>A| S266
16 BAA02g35060 A02 30152292 C T downstream_gene_variant MODIFIER c.*1175G>A| S2
17 BAA02g35060 A02 30152351 C T downstream_gene_variant MODIFIER c.*1116G>A| S299
18 BAA02g35060 A02 30152482 G A downstream_gene_variant MODIFIER c.*985C>T| S58
19 BAA02g35060 A02 30152754 G A downstream_gene_variant MODIFIER c.*713C>T| S47
20 BAA02g35060 A02 30152864 C T downstream_gene_variant MODIFIER c.*603G>A| S239
21 BAA02g35060 A02 30152911 C T downstream_gene_variant MODIFIER c.*556G>A| S130
22 BAA02g35060 A02 30152932 G A downstream_gene_variant MODIFIER c.*535C>T| S10
23 BAA02g35060 A02 30152975 G A downstream_gene_variant MODIFIER c.*492C>T| S268
24 BAA02g35060 A02 30154919 C T intron_variant MODIFIER c.199-818G>A| S162
25 BAA02g35060 A02 30155122 C T intron_variant MODIFIER c.198+812G>A| S15
S3