Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16730 | A09 | 9823092 | C | T | upstream_gene_variant | MODIFIER | c.-3455C>T| |
S231 |
2 | BAA09g16730 | A09 | 9823310 | G | A | upstream_gene_variant | MODIFIER | c.-3237G>A| |
S273 |
3 | BAA09g16730 | A09 | 9823465 | G | A | upstream_gene_variant | MODIFIER | c.-3082G>A| |
S25 |
4 | BAA09g16730 | A09 | 9824176 | C | T | upstream_gene_variant | MODIFIER | c.-2371C>T| |
S60 |
5 | BAA09g16730 | A09 | 9824279 | C | T | upstream_gene_variant | MODIFIER | c.-2268C>T| |
S135 |
6 | BAA09g16730 | A09 | 9825019 | G | A | upstream_gene_variant | MODIFIER | c.-1528G>A| |
S46 |
7 | BAA09g16730 | A09 | 9826082 | C | T | upstream_gene_variant | MODIFIER | c.-465C>T| |
S5 |
8 | BAA09g16730 | A09 | 9826177 | C | T | upstream_gene_variant | MODIFIER | c.-370C>T| |
S208 S93 |
9 | BAA09g16730 | A09 | 9826430 | G | A | upstream_gene_variant | MODIFIER | c.-117G>A| |
S165 S211 S227 |
10 | BAA09g16730 | A09 | 9826706 | C | T | missense_variant | MODERATE | c.160C>T|p.Leu54Phe |
S140 |
11 | BAA09g16730 | A09 | 9826967 | G | A | intron_variant | MODIFIER | c.313+108G>A| |
S238 |
12 | BAA09g16730 | A09 | 9827124 | G | A | intron_variant | MODIFIER | c.313+265G>A| |
S165 |
13 | BAA09g16730 | A09 | 9827163 | G | A | intron_variant | MODIFIER | c.313+304G>A| |
S233 |
14 | BAA09g16730 | A09 | 9828721 | C | T | intron_variant | MODIFIER | c.314-1341C>T| |
S143 |
15 | BAA09g16730 | A09 | 9829384 | G | A | intron_variant | MODIFIER | c.314-678G>A| |
S219 S72 |
16 | BAA09g16730 | A09 | 9829562 | G | A | intron_variant | MODIFIER | c.314-500G>A| |
S298 |
17 | BAA09g16730 | A09 | 9829662 | G | A | intron_variant | MODIFIER | c.314-400G>A| |
S105 S106 |
18 | BAA09g16730 | A09 | 9829834 | G | A | intron_variant | MODIFIER | c.314-228G>A| |
S182 |
19 | BAA09g16730 | A09 | 9829989 | C | T | intron_variant | MODIFIER | c.314-73C>T| |
S68 |
20 | BAA09g16730 | A09 | 9830488 | C | T | intron_variant | MODIFIER | c.665+75C>T| |
S269 |
21 | BAA09g16730 | A09 | 9830885 | G | A | missense_variant | MODERATE | c.806G>A|p.Gly269Glu |
S112 |