| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 177701 | BAA02g18920 | A02 | 9785796 | C | T | upstream_gene_variant | MODIFIER | c.-2772G>A| |
S270 |
| 177702 | BAA02g18920 | A02 | 9786617 | G | A | upstream_gene_variant | MODIFIER | c.-3593C>T| |
S116 |
| 177703 | BAA02g18920 | A02 | 9786843 | G | A | upstream_gene_variant | MODIFIER | c.-3819C>T| |
S155 |
| 177704 | BAA02g18920 | A02 | 9787016 | C | T | upstream_gene_variant | MODIFIER | c.-3992G>A| |
S138 |
| 177705 | BAA02g18920 | A02 | 9787276 | C | T | upstream_gene_variant | MODIFIER | c.-4252G>A| |
S47 |
| 177706 | BAA02g18940 | A02 | 9787438 | G | A | synonymous_variant | LOW | c.33G>A|p.Gln11Gln |
S199 |
| 177707 | BAA02g18920 | A02 | 9787607 | G | A | upstream_gene_variant | MODIFIER | c.-4583C>T| |
S37 |
| 177708 | BAA02g18930 | A02 | 9788524 | C | T | upstream_gene_variant | MODIFIER | c.-3396G>A| |
S118 |
| 177709 | BAA02g18930 | A02 | 9789037 | G | A | upstream_gene_variant | MODIFIER | c.-3909C>T| |
S13 S140 S168 S279 S64 |
| 177710 | BAA02g18930 | A02 | 9789199 | C | T | upstream_gene_variant | MODIFIER | c.-4071G>A| |
S161 |
| 177711 | BAA02g18930 | A02 | 9789522 | G | A | upstream_gene_variant | MODIFIER | c.-4394C>T| |
S116 |
| 177712 | BAA02g18930 | A02 | 9789705 | C | T | upstream_gene_variant | MODIFIER | c.-4577G>A| |
S242 |
| 177713 | BAA02g18950 | A02 | 9791287 | G | A | upstream_gene_variant | MODIFIER | c.-2123G>A| |
S287 |
| 177714 | BAA02g18950 | A02 | 9792150 | C | T | upstream_gene_variant | MODIFIER | c.-1260C>T| |
S289 S290 |
| 177715 | BAA02g18950 | A02 | 9792383 | C | T | upstream_gene_variant | MODIFIER | c.-1027C>T| |
S120 |
| 177716 | BAA02g18950 | A02 | 9792616 | G | A | upstream_gene_variant | MODIFIER | c.-794G>A| |
S23 |
| 177717 | BAA02g18950 | A02 | 9793267 | C | T | upstream_gene_variant | MODIFIER | c.-143C>T| |
S292 |
| 177718 | BAA02g18950 | A02 | 9793627 | G | A | missense_variant | MODERATE | c.218G>A|p.Gly73Asp |
S202 |
| 177719 | BAA02g18950 | A02 | 9794092 | G | A | stop_gained | HIGH | c.609G>A|p.Trp203* |
S223 |
| 177720 | BAA02g18960 | A02 | 9794646 | C | T | upstream_gene_variant | MODIFIER | c.-1693C>T| |
S46 |
| 177721 | BAA02g18950 | A02 | 9796907 | G | A | downstream_gene_variant | MODIFIER | c.*1935G>A| |
S204 |
| 177722 | BAA02g18960 | A02 | 9798831 | G | A | missense_variant | MODERATE | c.1348G>A|p.Asp450Asn |
S232 |
| 177723 | BAA02g18950 | A02 | 9799799 | G | A | downstream_gene_variant | MODIFIER | c.*4827G>A| |
S20 |
| 177724 | BAA02g18960 | A02 | 9800264 | G | A | downstream_gene_variant | MODIFIER | c.*1380G>A| |
S23 |
| 177725 | BAA02g18960 | A02 | 9802144 | G | A | downstream_gene_variant | MODIFIER | c.*3260G>A| |
S132 S137 S215 S237 S238 S288 |