| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g35350 | A01 | 23655195 | C | T | downstream_gene_variant | MODIFIER | c.*4842G>A| |
S238 |
| 2 | BAA01g35350 | A01 | 23660050 | C | T | missense_variant | MODERATE | c.581G>A|p.Gly194Glu |
S247 S54 |
| 3 | BAA01g35350 | A01 | 23660316 | C | T | synonymous_variant | LOW | c.315G>A|p.Glu105Glu |
S162 |
| 4 | BAA01g35350 | A01 | 23660425 | G | A | missense_variant | MODERATE | c.206C>T|p.Ala69Val |
S217 |
| 5 | BAA01g35350 | A01 | 23660607 | C | T | synonymous_variant | LOW | c.24G>A|p.Arg8Arg |
S198 |
| 6 | BAA01g35350 | A01 | 23661867 | G | A | upstream_gene_variant | MODIFIER | c.-1237C>T| |
S174 |
| 7 | BAA01g35350 | A01 | 23662090 | G | A | upstream_gene_variant | MODIFIER | c.-1460C>T| |
S70 |
| 8 | BAA01g35350 | A01 | 23662151 | C | T | upstream_gene_variant | MODIFIER | c.-1521G>A| |
S273 |
| 9 | BAA01g35350 | A01 | 23662265 | C | T | upstream_gene_variant | MODIFIER | c.-1635G>A| |
S51 |
| 10 | BAA01g35350 | A01 | 23662759 | C | T | upstream_gene_variant | MODIFIER | c.-2129G>A| |
S110 |
| 11 | BAA01g35350 | A01 | 23662762 | C | T | upstream_gene_variant | MODIFIER | c.-2132G>A| |
S264 |
| 12 | BAA01g35350 | A01 | 23663019 | G | A | upstream_gene_variant | MODIFIER | c.-2389C>T| |
S35 |
| 13 | BAA01g35350 | A01 | 23663551 | C | T | upstream_gene_variant | MODIFIER | c.-2921G>A| |
S46 |
| 14 | BAA01g35350 | A01 | 23663709 | G | A | upstream_gene_variant | MODIFIER | c.-3079C>T| |
S267 |
| 15 | BAA01g35350 | A01 | 23663865 | C | T | upstream_gene_variant | MODIFIER | c.-3235G>A| |
S166 |
| 16 | BAA01g35350 | A01 | 23664567 | C | T | upstream_gene_variant | MODIFIER | c.-3937G>A| |
S284 |
| 17 | BAA01g35350 | A01 | 23665363 | G | A | upstream_gene_variant | MODIFIER | c.-4733C>T| |
S229 |