| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g04850 | A03 | 2054689 | C | T | missense_variant | MODERATE | c.3550G>A|p.Val1184Met |
S142 |
| 2 | BAA03g04850 | A03 | 2055441 | C | T | missense_variant | MODERATE | c.2798G>A|p.Arg933Lys |
S224 |
| 3 | BAA03g04850 | A03 | 2055603 | G | A | missense_variant | MODERATE | c.2636C>T|p.Pro879Leu |
S125 |
| 4 | BAA03g04850 | A03 | 2056122 | C | T | missense_variant | MODERATE | c.2117G>A|p.Cys706Tyr |
S134 |
| 5 | BAA03g04850 | A03 | 2056445 | C | T | missense_variant | MODERATE | c.1971G>A|p.Met657Ile |
S293 |
| 6 | BAA03g04850 | A03 | 2056670 | C | T | synonymous_variant | LOW | c.1746G>A|p.Lys582Lys |
S32 |
| 7 | BAA03g04850 | A03 | 2056957 | G | A | synonymous_variant | LOW | c.1548C>T|p.Val516Val |
S176 |
| 8 | BAA03g04850 | A03 | 2057206 | C | T | synonymous_variant | LOW | c.1299G>A|p.Leu433Leu |
S233 |
| 9 | BAA03g04850 | A03 | 2057307 | G | A | missense_variant | MODERATE | c.1198C>T|p.Leu400Phe |
S150 |
| 10 | BAA03g04850 | A03 | 2057581 | C | T | synonymous_variant | LOW | c.924G>A|p.Leu308Leu |
S210 S225 |
| 11 | BAA03g04850 | A03 | 2058138 | C | T | missense_variant | MODERATE | c.463G>A|p.Val155Met |
S166 |
| 12 | BAA03g04850 | A03 | 2058743 | C | T | upstream_gene_variant | MODIFIER | c.-143G>A| |
S293 |
| 13 | BAA03g04850 | A03 | 2058809 | C | T | upstream_gene_variant | MODIFIER | c.-209G>A| |
S138 |