| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 218501 | BAA02g32930 | A02 | 28187796 | G | A | upstream_gene_variant | MODIFIER | c.-1110G>A| |
S176 |
| 218502 | BAA02g32930 | A02 | 28187974 | G | A | upstream_gene_variant | MODIFIER | c.-932G>A| |
S306 S308 |
| 218503 | BAA02g32940 | A02 | 28189699 | C | T | upstream_gene_variant | MODIFIER | c.-2671C>T| |
S282 |
| 218504 | BAA02g32940 | A02 | 28189882 | G | A | upstream_gene_variant | MODIFIER | c.-2488G>A| |
S293 |
| 218505 | BAA02g32940 | A02 | 28190159 | G | A | upstream_gene_variant | MODIFIER | c.-2211G>A| |
S287 |
| 218506 | BAA02g32940 | A02 | 28190699 | C | T | upstream_gene_variant | MODIFIER | c.-1671C>T| |
S73 |
| 218507 | BAA02g32940 | A02 | 28190834 | G | A | upstream_gene_variant | MODIFIER | c.-1536G>A| |
S276 |
| 218508 | BAA02g32940 | A02 | 28190923 | G | A | upstream_gene_variant | MODIFIER | c.-1447G>A| |
S184 |
| 218509 | BAA02g32940 | A02 | 28191044 | C | T | upstream_gene_variant | MODIFIER | c.-1326C>T| |
S45 |
| 218510 | BAA02g32940 | A02 | 28192036 | C | T | upstream_gene_variant | MODIFIER | c.-334C>T| |
S173 |
| 218511 | BAA02g32940 | A02 | 28192461 | G | A | missense_variant | MODERATE | c.92G>A|p.Gly31Asp |
S224 |
| 218512 | BAA02g32940 | A02 | 28192872 | C | T | missense_variant | MODERATE | c.214C>T|p.His72Tyr |
S249 |
| 218513 | BAA02g32940 | A02 | 28192898 | G | A | synonymous_variant | LOW | c.240G>A|p.Val80Val |
S37 |
| 218514 | BAA02g32930 | A02 | 28193121 | C | T | downstream_gene_variant | MODIFIER | c.*4024C>T| |
S277 |
| 218515 | BAA02g32940 | A02 | 28193391 | C | T | missense_variant | MODERATE | c.637C>T|p.Pro213Ser |
S181 S202 |
| 218516 | BAA02g32940 | A02 | 28193963 | G | A | synonymous_variant | LOW | c.1209G>A|p.Pro403Pro |
S74 |
| 218517 | BAA02g32940 | A02 | 28193999 | C | T | synonymous_variant | LOW | c.1245C>T|p.Leu415Leu |
S68 |
| 218518 | BAA02g32940 | A02 | 28195054 | C | T | downstream_gene_variant | MODIFIER | c.*722C>T| |
S274 |
| 218519 | BAA02g32940 | A02 | 28195164 | G | A | downstream_gene_variant | MODIFIER | c.*832G>A| |
S228 |
| 218520 | BAA02g32940 | A02 | 28195420 | G | A | downstream_gene_variant | MODIFIER | c.*1088G>A| |
S232 |
| 218521 | BAA02g32940 | A02 | 28195850 | G | A | downstream_gene_variant | MODIFIER | c.*1518G>A| |
S133 |
| 218522 | BAA02g32940 | A02 | 28198168 | G | A | downstream_gene_variant | MODIFIER | c.*3836G>A| |
S58 |
| 218523 | BAA02g32950 | A02 | 28201123 | C | T | downstream_gene_variant | MODIFIER | c.*3332G>A| |
S18 |
| 218524 | BAA02g32950 | A02 | 28203678 | G | A | downstream_gene_variant | MODIFIER | c.*777C>T| |
S176 |
| 218525 | BAA02g32950 | A02 | 28204922 | G | A | intron_variant | MODIFIER | c.376-9C>T| |
S187 |