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


Gene ID

Results: 1 - 34 of 34 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g27390 A02 15394822 G A upstream_gene_variant MODIFIER c.-3699G>A| S245
2 BAA02g27390 A02 15395245 G A upstream_gene_variant MODIFIER c.-3276G>A| S56
3 BAA02g27390 A02 15395775 C T upstream_gene_variant MODIFIER c.-2746C>T| S282
4 BAA02g27390 A02 15396675 G A upstream_gene_variant MODIFIER c.-1846G>A| S45
5 BAA02g27390 A02 15397639 G A upstream_gene_variant MODIFIER c.-882G>A| S286
6 BAA02g27390 A02 15398724 C T intron_variant MODIFIER c.46+158C>T| S203
7 BAA02g27390 A02 15399534 G A intron_variant MODIFIER c.46+968G>A| S92
8 BAA02g27390 A02 15399799 C T intron_variant MODIFIER c.47-978C>T| S183
S198
9 BAA02g27390 A02 15400952 C T splice_region_variant&intron_variant LOW c.214+8C>T| S289
S290
10 BAA02g27390 A02 15402336 C T missense_variant MODERATE c.1129C>T|p.Leu377Phe S221
11 BAA02g27390 A02 15402731 C T intron_variant MODIFIER c.1440+84C>T| S40
12 BAA02g27390 A02 15403105 C T intron_variant MODIFIER c.1441-294C>T| S135
13 BAA02g27390 A02 15403148 G A intron_variant MODIFIER c.1441-251G>A| S136
14 BAA02g27390 A02 15403227 G A intron_variant MODIFIER c.1441-172G>A| S186
15 BAA02g27390 A02 15403340 C T intron_variant MODIFIER c.1441-59C>T| S283
16 BAA02g27390 A02 15403360 G A intron_variant MODIFIER c.1441-39G>A| S149
17 BAA02g27390 A02 15403753 C T stop_gained HIGH c.1795C>T|p.Gln599* S176
18 BAA02g27390 A02 15403931 C T missense_variant MODERATE c.1973C>T|p.Ser658Phe S127
19 BAA02g27390 A02 15404792 C T intron_variant MODIFIER c.2716+118C>T| S171
20 BAA02g27390 A02 15404925 G A intron_variant MODIFIER c.2716+251G>A| S113
21 BAA02g27390 A02 15405477 G A intron_variant MODIFIER c.2716+803G>A| S10
22 BAA02g27390 A02 15406646 G A intron_variant MODIFIER c.2716+1972G>A| S293
23 BAA02g27390 A02 15406836 G A intron_variant MODIFIER c.2716+2162G>A| S10
24 BAA02g27390 A02 15409033 G A intron_variant MODIFIER c.2717-462G>A| S196
25 BAA02g27390 A02 15409155 C T intron_variant MODIFIER c.2717-340C>T| S100