Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19570 | A02 | 10170170 | G | A | downstream_gene_variant | MODIFIER | c.*1934C>T| |
S92 |
2 | BAA02g19570 | A02 | 10170945 | C | T | downstream_gene_variant | MODIFIER | c.*1159G>A| |
S156 S34 |
3 | BAA02g19570 | A02 | 10171083 | G | A | downstream_gene_variant | MODIFIER | c.*1021C>T| |
S188 |
4 | BAA02g19570 | A02 | 10172531 | C | T | intron_variant | MODIFIER | c.253-118G>A| |
S216 S241 S265 S39 |
5 | BAA02g19570 | A02 | 10172834 | C | T | intron_variant | MODIFIER | c.143-27G>A| |
S71 |
6 | BAA02g19570 | A02 | 10173177 | G | A | upstream_gene_variant | MODIFIER | c.-65C>T| |
S35 |
7 | BAA02g19570 | A02 | 10173243 | G | A | upstream_gene_variant | MODIFIER | c.-131C>T| |
S122 |
8 | BAA02g19570 | A02 | 10173969 | G | A | upstream_gene_variant | MODIFIER | c.-857C>T| |
S33 |
9 | BAA02g19570 | A02 | 10174369 | G | A | upstream_gene_variant | MODIFIER | c.-1257C>T| |
S11 |
10 | BAA02g19570 | A02 | 10175079 | C | T | upstream_gene_variant | MODIFIER | c.-1967G>A| |
S171 |
11 | BAA02g19570 | A02 | 10176163 | C | T | upstream_gene_variant | MODIFIER | c.-3051G>A| |
S205 |
12 | BAA02g19570 | A02 | 10176265 | G | A | upstream_gene_variant | MODIFIER | c.-3153C>T| |
S202 |
13 | BAA02g19570 | A02 | 10176791 | G | A | upstream_gene_variant | MODIFIER | c.-3679C>T| |
S247 |
14 | BAA02g19570 | A02 | 10176845 | G | A | upstream_gene_variant | MODIFIER | c.-3733C>T| |
S176 |
15 | BAA02g19570 | A02 | 10177396 | G | A | upstream_gene_variant | MODIFIER | c.-4284C>T| |
S41 |
16 | BAA02g19570 | A02 | 10177547 | C | T | upstream_gene_variant | MODIFIER | c.-4435G>A| |
S255 |