| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g06190 | A05 | 2991624 | C | T | missense_variant | MODERATE | c.2501G>A|p.Arg834Lys |
S35 |
| 2 | BAA05g06190 | A05 | 2991858 | C | T | missense_variant | MODERATE | c.2267G>A|p.Gly756Glu |
S140 |
| 3 | BAA05g06190 | A05 | 2991972 | C | T | missense_variant | MODERATE | c.2153G>A|p.Arg718Lys |
S211 |
| 4 | BAA05g06190 | A05 | 2992217 | G | A | synonymous_variant | LOW | c.1908C>T|p.Phe636Phe |
S244 |
| 5 | BAA05g06190 | A05 | 2993447 | C | T | intron_variant | MODIFIER | c.1188-388G>A| |
S88 |
| 6 | BAA05g06190 | A05 | 2996149 | C | T | upstream_gene_variant | MODIFIER | c.-708G>A| |
S250 |
| 7 | BAA05g06190 | A05 | 2996506 | G | A | upstream_gene_variant | MODIFIER | c.-1065C>T| |
S209 |
| 8 | BAA05g06190 | A05 | 2998664 | C | T | upstream_gene_variant | MODIFIER | c.-3223G>A| |
S216 |
| 9 | BAA05g06190 | A05 | 2999178 | G | A | upstream_gene_variant | MODIFIER | c.-3737C>T| |
S124 |
| 10 | BAA05g06190 | A05 | 2999822 | C | T | upstream_gene_variant | MODIFIER | c.-4381G>A| |
S162 |