| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g15690 | A09 | 9016353 | C | T | missense_variant | MODERATE | c.1330G>A|p.Ala444Thr |
S17 |
| 2 | BAA09g15690 | A09 | 9017251 | C | T | synonymous_variant | LOW | c.432G>A|p.Lys144Lys |
S270 |
| 3 | BAA09g15690 | A09 | 9017407 | G | A | synonymous_variant | LOW | c.366C>T|p.Leu122Leu |
S163 |
| 4 | BAA09g15690 | A09 | 9017633 | G | A | missense_variant | MODERATE | c.140C>T|p.Ser47Phe |
S99 |
| 5 | BAA09g15690 | A09 | 9020533 | C | T | upstream_gene_variant | MODIFIER | c.-2360G>A| |
S186 |
| 6 | BAA09g15690 | A09 | 9021702 | C | T | upstream_gene_variant | MODIFIER | c.-3529G>A| |
S293 S5 |
| 7 | BAA09g15690 | A09 | 9021855 | G | A | upstream_gene_variant | MODIFIER | c.-3682C>T| |
S40 S49 |
| 8 | BAA09g15690 | A09 | 9022084 | C | T | upstream_gene_variant | MODIFIER | c.-3911G>A| |
S282 |
| 9 | BAA09g15690 | A09 | 9022110 | C | T | upstream_gene_variant | MODIFIER | c.-3937G>A| |
S33 |
| 10 | BAA09g15690 | A09 | 9022217 | C | T | upstream_gene_variant | MODIFIER | c.-4044G>A| |
S87 |