| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 190801 | BAA02g26080 | A02 | 14447786 | G | A | missense_variant | MODERATE | c.597G>A|p.Met199Ile |
S95 |
| 190802 | BAA02g26080 | A02 | 14449527 | G | T | downstream_gene_variant | MODIFIER | c.*999G>T| |
S99 |
| 190803 | BAA02g26080 | A02 | 14450160 | G | A | downstream_gene_variant | MODIFIER | c.*1632G>A| |
S298 |
| 190804 | BAA02g26080 | A02 | 14450991 | C | T | downstream_gene_variant | MODIFIER | c.*2463C>T| |
S183 S198 |
| 190805 | BAA02g26080 | A02 | 14451734 | C | T | downstream_gene_variant | MODIFIER | c.*3206C>T| |
S216 |
| 190806 | BAA02g26080 | A02 | 14452728 | C | T | downstream_gene_variant | MODIFIER | c.*4200C>T| |
S139 |
| 190807 | BAA02g26080 | A02 | 14453237 | G | A | downstream_gene_variant | MODIFIER | c.*4709G>A| |
S217 |
| 190808 | BAA02g26090 | A02 | 14453630 | G | A | downstream_gene_variant | MODIFIER | c.*921C>T| |
S156 |
| 190809 | BAA02g26090 | A02 | 14453752 | G | A | downstream_gene_variant | MODIFIER | c.*799C>T| |
S146 S212 S259 S69 |
| 190810 | BAA02g26090 | A02 | 14456800 | G | A | synonymous_variant | LOW | c.3064C>T|p.Leu1022Leu |
S13 |
| 190811 | BAA02g26090 | A02 | 14457716 | G | A | intron_variant | MODIFIER | c.2730+16C>T| |
S232 |
| 190812 | BAA02g26090 | A02 | 14457955 | G | A | missense_variant | MODERATE | c.2585C>T|p.Ser862Leu |
S148 S30 S31 |
| 190813 | BAA02g26090 | A02 | 14458285 | C | T | intron_variant | MODIFIER | c.2481+123G>A| |
S161 |
| 190814 | BAA02g26090 | A02 | 14458433 | C | T | missense_variant | MODERATE | c.2456G>A|p.Gly819Asp |
S179 |
| 190815 | BAA02g26090 | A02 | 14460379 | G | A | missense_variant | MODERATE | c.1867C>T|p.Leu623Phe |
S208 |
| 190816 | BAA02g26100 | A02 | 14460562 | C | T | downstream_gene_variant | MODIFIER | c.*4589G>A| |
S49 |
| 190817 | BAA02g26090 | A02 | 14460756 | G | A | synonymous_variant | LOW | c.1779C>T|p.Ala593Ala |
S187 |
| 190818 | BAA02g26090 | A02 | 14461147 | G | A | missense_variant | MODERATE | c.1564C>T|p.Leu522Phe |
S240 |
| 190819 | BAA02g26090 | A02 | 14461710 | C | T | missense_variant | MODERATE | c.1175G>A|p.Arg392Lys |
S255 |
| 190820 | BAA02g26090 | A02 | 14463313 | C | T | missense_variant | MODERATE | c.191G>A|p.Arg64Lys |
S112 |
| 190821 | BAA02g26090 | A02 | 14463851 | G | A | upstream_gene_variant | MODIFIER | c.-82C>T| |
S25 |
| 190822 | BAA02g26090 | A02 | 14464713 | C | T | upstream_gene_variant | MODIFIER | c.-944G>A| |
S211 |
| 190823 | BAA02g26090 | A02 | 14464784 | C | T | upstream_gene_variant | MODIFIER | c.-1015G>A| |
S183 S198 |
| 190824 | BAA02g26090 | A02 | 14464821 | C | T | upstream_gene_variant | MODIFIER | c.-1052G>A| |
S121 |
| 190825 | BAA02g26090 | A02 | 14464858 | C | T | upstream_gene_variant | MODIFIER | c.-1089G>A| |
S18 |