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


Gene ID

Results: 1 - 30 of 30 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g39270 A02 33376755 C T upstream_gene_variant MODIFIER c.-4468C>T| S305
2 BAA02g39270 A02 33378278 C T upstream_gene_variant MODIFIER c.-2945C>T| S180
3 BAA02g39270 A02 33378791 G A upstream_gene_variant MODIFIER c.-2432G>A| S35
4 BAA02g39270 A02 33380385 C T upstream_gene_variant MODIFIER c.-838C>T| S168
5 BAA02g39270 A02 33380464 T C upstream_gene_variant MODIFIER c.-759T>C| S261
6 BAA02g39270 A02 33380606 C T upstream_gene_variant MODIFIER c.-617C>T| S107
7 BAA02g39270 A02 33382617 G A intron_variant MODIFIER c.44+1351G>A| S306
S308
8 BAA02g39270 A02 33382625 G A intron_variant MODIFIER c.44+1359G>A| S224
9 BAA02g39270 A02 33382750 G A intron_variant MODIFIER c.44+1484G>A| S255
10 BAA02g39270 A02 33382938 G A intron_variant MODIFIER c.44+1672G>A| S221
11 BAA02g39270 A02 33383058 C T intron_variant MODIFIER c.44+1792C>T| S239
12 BAA02g39270 A02 33383553 C T intron_variant MODIFIER c.44+2287C>T| S183
S198
13 BAA02g39270 A02 33383628 G A intron_variant MODIFIER c.44+2362G>A| S164
14 BAA02g39270 A02 33383729 G A intron_variant MODIFIER c.44+2463G>A| S51
15 BAA02g39270 A02 33383870 C T intron_variant MODIFIER c.44+2604C>T| S95
16 BAA02g39270 A02 33384047 C T intron_variant MODIFIER c.44+2781C>T| S189
17 BAA02g39270 A02 33384426 G A intron_variant MODIFIER c.44+3160G>A| S177
18 BAA02g39270 A02 33384612 C T intron_variant MODIFIER c.45-3291C>T| S128
19 BAA02g39270 A02 33386254 G A intron_variant MODIFIER c.45-1649G>A| S50
20 BAA02g39270 A02 33386269 G A intron_variant MODIFIER c.45-1634G>A| S80
21 BAA02g39270 A02 33386606 G A intron_variant MODIFIER c.45-1297G>A| S256
22 BAA02g39270 A02 33387124 C T intron_variant MODIFIER c.45-779C>T| S130
23 BAA02g39270 A02 33387918 A T synonymous_variant LOW c.60A>T|p.Leu20Leu S119
24 BAA02g39270 A02 33388813 G A intron_variant MODIFIER c.487+468G>A| S113
25 BAA02g39270 A02 33391305 G A intron_variant MODIFIER c.488-858G>A| S186