Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25740 | A02 | 14139850 | G | A | downstream_gene_variant | MODIFIER | c.*179C>T| |
S150 |
2 | BAA02g25740 | A02 | 14140165 | C | T | missense_variant | MODERATE | c.284G>A|p.Gly95Asp |
S105 S106 |
3 | BAA02g25740 | A02 | 14140271 | G | A | intron_variant | MODIFIER | c.202-24C>T| |
S269 |
4 | BAA02g25740 | A02 | 14140370 | G | A | intron_variant | MODIFIER | c.202-123C>T| |
S7 |
5 | BAA02g25740 | A02 | 14141076 | G | A | intron_variant | MODIFIER | c.201+568C>T| |
S187 |
6 | BAA02g25740 | A02 | 14141181 | G | T | intron_variant | MODIFIER | c.201+463C>A| |
S283 |
7 | BAA02g25740 | A02 | 14141560 | A | G | intron_variant | MODIFIER | c.201+84T>C| |
S80 |
8 | BAA02g25740 | A02 | 14143071 | G | A | upstream_gene_variant | MODIFIER | c.-1227C>T| |
S292 |
9 | BAA02g25740 | A02 | 14143518 | C | T | upstream_gene_variant | MODIFIER | c.-1674G>A| |
S9 |
10 | BAA02g25740 | A02 | 14144047 | G | A | upstream_gene_variant | MODIFIER | c.-2203C>T| |
S280 |
11 | BAA02g25740 | A02 | 14144615 | C | T | upstream_gene_variant | MODIFIER | c.-2771G>A| |
S192 |
12 | BAA02g25740 | A02 | 14144656 | C | T | upstream_gene_variant | MODIFIER | c.-2812G>A| |
S180 |
13 | BAA02g25740 | A02 | 14144775 | C | T | upstream_gene_variant | MODIFIER | c.-2931G>A| |
S94 |
14 | BAA02g25740 | A02 | 14145256 | C | T | upstream_gene_variant | MODIFIER | c.-3412G>A| |
S250 |
15 | BAA02g25740 | A02 | 14145939 | C | T | upstream_gene_variant | MODIFIER | c.-4095G>A| |
S250 |
16 | BAA02g25740 | A02 | 14146310 | G | A | upstream_gene_variant | MODIFIER | c.-4466C>T| |
S37 |
17 | BAA02g25740 | A02 | 14146696 | G | A | upstream_gene_variant | MODIFIER | c.-4852C>T| |
S272 |
18 | BAA02g25740 | A02 | 14146759 | C | T | upstream_gene_variant | MODIFIER | c.-4915G>A| |
S87 |