| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g11050 | A05 | 5614343 | C | T | missense_variant | MODERATE | c.1223G>A|p.Gly408Glu |
S63 |
| 2 | BAA05g11050 | A05 | 5614837 | C | T | missense_variant | MODERATE | c.794G>A|p.Gly265Glu |
S142 |
| 3 | BAA05g11050 | A05 | 5614941 | C | T | synonymous_variant | LOW | c.690G>A|p.Leu230Leu |
S168 |
| 4 | BAA05g11050 | A05 | 5614976 | C | T | missense_variant | MODERATE | c.655G>A|p.Glu219Lys |
S204 |
| 5 | BAA05g11050 | A05 | 5615238 | G | A | synonymous_variant | LOW | c.393C>T|p.Phe131Phe |
S126 |
| 6 | BAA05g11050 | A05 | 5615346 | G | A | synonymous_variant | LOW | c.285C>T|p.Phe95Phe |
S61 |
| 7 | BAA05g11050 | A05 | 5618920 | G | A | upstream_gene_variant | MODIFIER | c.-3290C>T| |
S280 |
| 8 | BAA05g11050 | A05 | 5619849 | A | C | upstream_gene_variant | MODIFIER | c.-4219T>G| |
S182 |
| 9 | BAA05g11050 | A05 | 5620077 | C | T | upstream_gene_variant | MODIFIER | c.-4447G>A| |
S295 |
| 10 | BAA05g11050 | A05 | 5620586 | C | T | upstream_gene_variant | MODIFIER | c.-4956G>A| |
S270 |