Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17900 | A02 | 8977404 | G | A | downstream_gene_variant | MODIFIER | c.*2599C>T| |
S188 |
2 | BAA02g17900 | A02 | 8977905 | C | T | downstream_gene_variant | MODIFIER | c.*2098G>A| |
S261 |
3 | BAA02g17900 | A02 | 8978472 | G | A | downstream_gene_variant | MODIFIER | c.*1531C>T| |
S231 |
4 | BAA02g17900 | A02 | 8979839 | G | A | downstream_gene_variant | MODIFIER | c.*164C>T| |
S122 |
5 | BAA02g17900 | A02 | 8980730 | G | A | intron_variant | MODIFIER | c.790-71C>T| |
S60 |
6 | BAA02g17900 | A02 | 8981070 | C | T | intron_variant | MODIFIER | c.790-411G>A| |
S75 S81 |
7 | BAA02g17900 | A02 | 8981249 | G | A | intron_variant | MODIFIER | c.789+277C>T| |
S109 |
8 | BAA02g17900 | A02 | 8982684 | G | A | intron_variant | MODIFIER | c.335-181C>T| |
S265 |
9 | BAA02g17900 | A02 | 8983483 | G | A | intron_variant | MODIFIER | c.334+760C>T| |
S33 |
10 | BAA02g17900 | A02 | 8984060 | C | T | intron_variant | MODIFIER | c.334+183G>A| |
S135 |
11 | BAA02g17900 | A02 | 8984172 | G | A | intron_variant | MODIFIER | c.334+71C>T| |
S168 |
12 | BAA02g17900 | A02 | 8984659 | C | T | intron_variant | MODIFIER | c.100+169G>A| |
S206 S26 |
13 | BAA02g17900 | A02 | 8984783 | G | A | intron_variant | MODIFIER | c.100+45C>T| |
S274 |
14 | BAA02g17900 | A02 | 8984890 | G | A | missense_variant | MODERATE | c.38C>T|p.Thr13Ile |
S59 |
15 | BAA02g17900 | A02 | 8986167 | G | A | upstream_gene_variant | MODIFIER | c.-1240C>T| |
S20 |
16 | BAA02g17900 | A02 | 8986282 | G | A | upstream_gene_variant | MODIFIER | c.-1355C>T| |
S129 |
17 | BAA02g17900 | A02 | 8988000 | G | A | upstream_gene_variant | MODIFIER | c.-3073C>T| |
S67 |
18 | BAA02g17900 | A02 | 8988352 | C | T | upstream_gene_variant | MODIFIER | c.-3425G>A| |
S103 |
19 | BAA02g17900 | A02 | 8988544 | G | A | upstream_gene_variant | MODIFIER | c.-3617C>T| |
S197 |
20 | BAA02g17900 | A02 | 8988983 | G | A | upstream_gene_variant | MODIFIER | c.-4056C>T| |
S193 |