| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g29400 | A02 | 16829359 | G | A | downstream_gene_variant | MODIFIER | c.*449C>T| |
S57 |
| 2 | BAA02g29400 | A02 | 16830743 | C | T | missense_variant | MODERATE | c.2122G>A|p.Asp708Asn |
S277 |
| 3 | BAA02g29400 | A02 | 16831571 | C | T | synonymous_variant | LOW | c.1371G>A|p.Lys457Lys |
S18 |
| 4 | BAA02g29400 | A02 | 16831592 | C | T | missense_variant | MODERATE | c.1350G>A|p.Met450Ile |
S63 |
| 5 | BAA02g29400 | A02 | 16832443 | G | A | missense_variant | MODERATE | c.979C>T|p.Arg327Cys |
S17 |
| 6 | BAA02g29400 | A02 | 16834666 | G | A | upstream_gene_variant | MODIFIER | c.-399C>T| |
S84 S93 |
| 7 | BAA02g29400 | A02 | 16835015 | G | A | upstream_gene_variant | MODIFIER | c.-748C>T| |
S94 |
| 8 | BAA02g29400 | A02 | 16835052 | C | T | upstream_gene_variant | MODIFIER | c.-785G>A| |
S275 |
| 9 | BAA02g29400 | A02 | 16835688 | C | T | upstream_gene_variant | MODIFIER | c.-1421G>A| |
S157 S163 |
| 10 | BAA02g29400 | A02 | 16835892 | C | T | upstream_gene_variant | MODIFIER | c.-1625G>A| |
S63 |
| 11 | BAA02g29400 | A02 | 16837360 | G | A | upstream_gene_variant | MODIFIER | c.-3093C>T| |
S50 |
| 12 | BAA02g29400 | A02 | 16837399 | G | A | upstream_gene_variant | MODIFIER | c.-3132C>T| |
S302 |
| 13 | BAA02g29400 | A02 | 16837929 | C | T | upstream_gene_variant | MODIFIER | c.-3662G>A| |
S108 |
| 14 | BAA02g29400 | A02 | 16838305 | C | T | upstream_gene_variant | MODIFIER | c.-4038G>A| |
S203 |
| 15 | BAA02g29400 | A02 | 16838784 | C | T | upstream_gene_variant | MODIFIER | c.-4517G>A| |
S121 |
| 16 | BAA02g29400 | A02 | 16838845 | C | T | upstream_gene_variant | MODIFIER | c.-4578G>A| |
S175 |