| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g34050 | A09 | 42587624 | G | A | upstream_gene_variant | MODIFIER | c.-853G>A| |
S167 |
| 2 | BAA09g34050 | A09 | 42588091 | G | A | upstream_gene_variant | MODIFIER | c.-386G>A| |
S37 |
| 3 | BAA09g34050 | A09 | 42588153 | G | A | upstream_gene_variant | MODIFIER | c.-324G>A| |
S37 |
| 4 | BAA09g34050 | A09 | 42588241 | G | A | upstream_gene_variant | MODIFIER | c.-236G>A| |
S13 |
| 5 | BAA09g34050 | A09 | 42588423 | C | T | upstream_gene_variant | MODIFIER | c.-54C>T| |
S286 |
| 6 | BAA09g34050 | A09 | 42588743 | G | A | splice_region_variant&synonymous_variant | LOW | c.21G>A|p.Pro7Pro |
S42 |
| 7 | BAA09g34050 | A09 | 42589334 | G | A | missense_variant | MODERATE | c.533G>A|p.Gly178Glu |
S71 |
| 8 | BAA09g34050 | A09 | 42589550 | C | T | missense_variant | MODERATE | c.665C>T|p.Ala222Val |
S122 |
| 9 | BAA09g34050 | A09 | 42589589 | C | T | missense_variant | MODERATE | c.704C>T|p.Thr235Ile |
S61 |
| 10 | BAA09g34050 | A09 | 42589882 | C | T | synonymous_variant | LOW | c.907C>T|p.Leu303Leu |
S32 |
| 11 | BAA09g34050 | A09 | 42590172 | C | T | missense_variant | MODERATE | c.1043C>T|p.Ala348Val |
S245 |
| 12 | BAA09g34050 | A09 | 42591991 | G | A | downstream_gene_variant | MODIFIER | c.*274G>A| |
S111 |
| 13 | BAA09g34050 | A09 | 42592092 | C | T | downstream_gene_variant | MODIFIER | c.*375C>T| |
S247 |
| 14 | BAA09g34050 | A09 | 42592101 | C | T | downstream_gene_variant | MODIFIER | c.*384C>T| |
S159 S243 S299 |