| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g11690 | A06 | 5919713 | C | T | upstream_gene_variant | MODIFIER | c.-2900C>T| |
S187 |
| 2 | BAA06g11690 | A06 | 5919818 | G | A | upstream_gene_variant | MODIFIER | c.-2795G>A| |
S144 |
| 3 | BAA06g11690 | A06 | 5919880 | G | A | upstream_gene_variant | MODIFIER | c.-2733G>A| |
S13 |
| 4 | BAA06g11690 | A06 | 5920525 | C | T | upstream_gene_variant | MODIFIER | c.-2088C>T| |
S250 |
| 5 | BAA06g11690 | A06 | 5921524 | C | T | upstream_gene_variant | MODIFIER | c.-1089C>T| |
S132 S137 S215 |
| 6 | BAA06g11690 | A06 | 5921877 | C | T | upstream_gene_variant | MODIFIER | c.-736C>T| |
S211 |
| 7 | BAA06g11690 | A06 | 5922990 | G | A | synonymous_variant | LOW | c.378G>A|p.Glu126Glu |
S9 |
| 8 | BAA06g11690 | A06 | 5923019 | C | T | missense_variant | MODERATE | c.407C>T|p.Thr136Met |
S210 |
| 9 | BAA06g11690 | A06 | 5925328 | G | A | downstream_gene_variant | MODIFIER | c.*2110G>A| |
S292 |
| 10 | BAA06g11690 | A06 | 5925981 | G | A | downstream_gene_variant | MODIFIER | c.*2763G>A| |
S152 |
| 11 | BAA06g11690 | A06 | 5927738 | C | T | downstream_gene_variant | MODIFIER | c.*4520C>T| |
S172 S217 |