Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13940 | A09 | 8023102 | C | T | upstream_gene_variant | MODIFIER | c.-3555C>T| |
S67 |
2 | BAA09g13940 | A09 | 8025745 | G | A | upstream_gene_variant | MODIFIER | c.-912G>A| |
S123 |
3 | BAA09g13940 | A09 | 8026690 | C | T | missense_variant | MODERATE | c.34C>T|p.Arg12Cys |
S36 |
4 | BAA09g13940 | A09 | 8026913 | C | T | missense_variant | MODERATE | c.257C>T|p.Ala86Val |
S68 |
5 | BAA09g13940 | A09 | 8029173 | G | A | missense_variant | MODERATE | c.958G>A|p.Val320Ile |
S12 |
6 | BAA09g13940 | A09 | 8029618 | G | A | missense_variant | MODERATE | c.1403G>A|p.Gly468Asp |
S73 S91 |
7 | BAA09g13940 | A09 | 8029738 | G | A | missense_variant | MODERATE | c.1523G>A|p.Arg508Lys |
S140 S168 S279 S64 |
8 | BAA09g13940 | A09 | 8030654 | C | T | missense_variant | MODERATE | c.2171C>T|p.Pro724Leu |
S84 S93 |
9 | BAA09g13940 | A09 | 8031165 | G | A | missense_variant | MODERATE | c.2612G>A|p.Gly871Glu |
S236 |
10 | BAA09g13940 | A09 | 8033081 | G | A | downstream_gene_variant | MODIFIER | c.*1528G>A| |
S85 |
11 | BAA09g13940 | A09 | 8033177 | G | A | downstream_gene_variant | MODIFIER | c.*1624G>A| |
S115 S122 S266 S297 S55 |
12 | BAA09g13940 | A09 | 8033961 | G | A | downstream_gene_variant | MODIFIER | c.*2408G>A| |
S152 |