| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g34310 | A09 | 42767574 | G | A | downstream_gene_variant | MODIFIER | c.*2342C>T| |
S116 |
| 2 | BAA09g34310 | A09 | 42767799 | C | T | downstream_gene_variant | MODIFIER | c.*2117G>A| |
S144 |
| 3 | BAA09g34310 | A09 | 42768757 | T | A | downstream_gene_variant | MODIFIER | c.*1159A>T| |
S146 S259 |
| 4 | BAA09g34310 | A09 | 42769433 | G | A | downstream_gene_variant | MODIFIER | c.*483C>T| |
S185 |
| 5 | BAA09g34310 | A09 | 42770185 | C | T | missense_variant | MODERATE | c.1174G>A|p.Val392Met |
S142 |
| 6 | BAA09g34310 | A09 | 42770214 | C | T | missense_variant | MODERATE | c.1145G>A|p.Arg382Lys |
S247 |
| 7 | BAA09g34310 | A09 | 42770298 | C | T | missense_variant | MODERATE | c.1061G>A|p.Gly354Glu |
S295 |
| 8 | BAA09g34310 | A09 | 42771260 | C | T | intron_variant | MODIFIER | c.548+360G>A| |
S282 |
| 9 | BAA09g34310 | A09 | 42772480 | C | T | intron_variant | MODIFIER | c.152-464G>A| |
S54 |
| 10 | BAA09g34310 | A09 | 42772682 | C | T | intron_variant | MODIFIER | c.151+329G>A| |
S64 |
| 11 | BAA09g34310 | A09 | 42772776 | G | A | intron_variant | MODIFIER | c.151+235C>T| |
S170 |
| 12 | BAA09g34310 | A09 | 42772843 | C | T | intron_variant | MODIFIER | c.151+168G>A| |
S36 |
| 13 | BAA09g34310 | A09 | 42773131 | G | A | missense_variant | MODERATE | c.31C>T|p.Leu11Phe |
S218 |
| 14 | BAA09g34310 | A09 | 42773801 | C | T | upstream_gene_variant | MODIFIER | c.-640G>A| |
S301 S304 |
| 15 | BAA09g34310 | A09 | 42774351 | G | A | upstream_gene_variant | MODIFIER | c.-1190C>T| |
S148 |
| 16 | BAA09g34310 | A09 | 42775807 | C | T | upstream_gene_variant | MODIFIER | c.-2646G>A| |
S293 |
| 17 | BAA09g34310 | A09 | 42775906 | C | T | upstream_gene_variant | MODIFIER | c.-2745G>A| |
S57 |
| 18 | BAA09g34310 | A09 | 42777644 | C | T | upstream_gene_variant | MODIFIER | c.-4483G>A| |
S272 |
| 19 | BAA09g34310 | A09 | 42778095 | C | T | upstream_gene_variant | MODIFIER | c.-4934G>A| |
S86 |