| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g11400 | A06 | 5761425 | C | T | upstream_gene_variant | MODIFIER | c.-1434C>T| |
S267 |
| 2 | BAA06g11400 | A06 | 5761513 | C | T | upstream_gene_variant | MODIFIER | c.-1346C>T| |
S130 |
| 3 | BAA06g11400 | A06 | 5764088 | C | T | missense_variant | MODERATE | c.443C>T|p.Ala148Val |
S302 |
| 4 | BAA06g11400 | A06 | 5764104 | C | T | synonymous_variant | LOW | c.459C>T|p.Gly153Gly |
S223 |
| 5 | BAA06g11400 | A06 | 5764180 | C | T | missense_variant | MODERATE | c.535C>T|p.Leu179Phe |
S161 |
| 6 | BAA06g11400 | A06 | 5764283 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.562-1G>A| |
S133 |
| 7 | BAA06g11400 | A06 | 5764967 | G | A | missense_variant | MODERATE | c.1006G>A|p.Ala336Thr |
S173 |