Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26150 | A02 | 14488135 | C | T | downstream_gene_variant | MODIFIER | c.*433G>A| |
S116 |
2 | BAA02g26150 | A02 | 14489129 | C | T | intron_variant | MODIFIER | c.2631+32G>A| |
S226 |
3 | BAA02g26150 | A02 | 14489355 | G | A | missense_variant | MODERATE | c.2437C>T|p.His813Tyr |
S297 |
4 | BAA02g26150 | A02 | 14489838 | G | A | missense_variant | MODERATE | c.1954C>T|p.Leu652Phe |
S85 |
5 | BAA02g26150 | A02 | 14490172 | G | A | synonymous_variant | LOW | c.1620C>T|p.Phe540Phe |
S202 |
6 | BAA02g26150 | A02 | 14491085 | G | A | missense_variant | MODERATE | c.707C>T|p.Ala236Val |
S259 |
7 | BAA02g26150 | A02 | 14491473 | G | A | intron_variant | MODIFIER | c.481-38C>T| |
S153 S213 |
8 | BAA02g26150 | A02 | 14491637 | C | T | intron_variant | MODIFIER | c.426+17G>A| |
S174 |
9 | BAA02g26150 | A02 | 14491796 | G | A | missense_variant | MODERATE | c.284C>T|p.Ser95Phe |
S62 |
10 | BAA02g26150 | A02 | 14492083 | G | A | stop_gained | HIGH | c.103C>T|p.Arg35* |
S251 |
11 | BAA02g26150 | A02 | 14492555 | G | A | upstream_gene_variant | MODIFIER | c.-370C>T| |
S157 |
12 | BAA02g26150 | A02 | 14492687 | G | A | upstream_gene_variant | MODIFIER | c.-502C>T| |
S62 |
13 | BAA02g26150 | A02 | 14493195 | C | T | upstream_gene_variant | MODIFIER | c.-1010G>A| |
S41 |
14 | BAA02g26150 | A02 | 14494289 | G | A | upstream_gene_variant | MODIFIER | c.-2104C>T| |
S109 |
15 | BAA02g26150 | A02 | 14494756 | C | T | upstream_gene_variant | MODIFIER | c.-2571G>A| |
S171 |
16 | BAA02g26150 | A02 | 14495324 | G | A | upstream_gene_variant | MODIFIER | c.-3139C>T| |
S25 |
17 | BAA02g26150 | A02 | 14495456 | G | A | upstream_gene_variant | MODIFIER | c.-3271C>T| |
S169 |
18 | BAA02g26150 | A02 | 14496531 | G | A | upstream_gene_variant | MODIFIER | c.-4346C>T| |
S203 |