| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g17670 | A01 | 8574345 | G | A | downstream_gene_variant | MODIFIER | c.*2419C>T| |
S224 |
| 2 | BAA01g17670 | A01 | 8574395 | G | A | downstream_gene_variant | MODIFIER | c.*2369C>T| |
S23 |
| 3 | BAA01g17670 | A01 | 8576994 | C | T | missense_variant | MODERATE | c.1492G>A|p.Asp498Asn |
S67 |
| 4 | BAA01g17670 | A01 | 8577347 | G | A | missense_variant | MODERATE | c.1139C>T|p.Ser380Leu |
S202 |
| 5 | BAA01g17670 | A01 | 8577484 | G | A | synonymous_variant | LOW | c.1002C>T|p.Leu334Leu |
S228 |
| 6 | BAA01g17670 | A01 | 8577758 | C | T | missense_variant | MODERATE | c.728G>A|p.Gly243Glu |
S171 |
| 7 | BAA01g17670 | A01 | 8577794 | C | T | missense_variant | MODERATE | c.692G>A|p.Arg231Lys |
S107 |
| 8 | BAA01g17670 | A01 | 8578298 | G | A | missense_variant | MODERATE | c.188C>T|p.Ala63Val |
S163 |
| 9 | BAA01g17670 | A01 | 8579751 | G | A | upstream_gene_variant | MODIFIER | c.-1266C>T| |
S162 |
| 10 | BAA01g17670 | A01 | 8579913 | G | A | upstream_gene_variant | MODIFIER | c.-1428C>T| |
S97 |
| 11 | BAA01g17670 | A01 | 8580766 | C | T | upstream_gene_variant | MODIFIER | c.-2281G>A| |
S8 |
| 12 | BAA01g17670 | A01 | 8581781 | C | T | upstream_gene_variant | MODIFIER | c.-3296G>A| |
S66 |
| 13 | BAA01g17670 | A01 | 8582035 | C | T | upstream_gene_variant | MODIFIER | c.-3550G>A| |
S71 |
| 14 | BAA01g17670 | A01 | 8582054 | G | A | upstream_gene_variant | MODIFIER | c.-3569C>T| |
S239 |