| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g41490 | A06 | 26998070 | C | T | upstream_gene_variant | MODIFIER | c.-1106C>T| |
S308 |
| 2 | BAA06g41490 | A06 | 26998269 | C | T | upstream_gene_variant | MODIFIER | c.-907C>T| |
S111 |
| 3 | BAA06g41490 | A06 | 26999040 | G | A | upstream_gene_variant | MODIFIER | c.-136G>A| |
S162 |
| 4 | BAA06g41490 | A06 | 26999246 | G | A | missense_variant | MODERATE | c.71G>A|p.Gly24Asp |
S87 |
| 5 | BAA06g41490 | A06 | 27001226 | C | T | missense_variant | MODERATE | c.718C>T|p.Leu240Phe |
S180 |
| 6 | BAA06g41490 | A06 | 27001525 | C | T | synonymous_variant | LOW | c.1017C>T|p.Phe339Phe |
S34 |
| 7 | BAA06g41490 | A06 | 27003043 | C | T | downstream_gene_variant | MODIFIER | c.*1014C>T| |
S156 S213 S4 S6 |
| 8 | BAA06g41490 | A06 | 27003758 | G | A | downstream_gene_variant | MODIFIER | c.*1729G>A| |
S249 |
| 9 | BAA06g41490 | A06 | 27005466 | G | A | downstream_gene_variant | MODIFIER | c.*3437G>A| |
S271 |
| 10 | BAA06g41490 | A06 | 27005955 | C | T | downstream_gene_variant | MODIFIER | c.*3926C>T| |
S259 |
| 11 | BAA06g41490 | A06 | 27006121 | G | T | downstream_gene_variant | MODIFIER | c.*4092G>T| |
S297 |
| 12 | BAA06g41490 | A06 | 27006723 | G | A | downstream_gene_variant | MODIFIER | c.*4694G>A| |
S162 |