| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 166101 | BAA02g12220 | A02 | 5511193 | C | T | upstream_gene_variant | MODIFIER | c.-3998G>A| |
S6 |
| 166102 | BAA02g12220 | A02 | 5511561 | G | A | upstream_gene_variant | MODIFIER | c.-4366C>T| |
S23 |
| 166103 | BAA02g12220 | A02 | 5511846 | C | T | upstream_gene_variant | MODIFIER | c.-4651G>A| |
S174 |
| 166104 | BAA02g12230 | A02 | 5512608 | G | A | downstream_gene_variant | MODIFIER | c.*300C>T| |
S217 |
| 166105 | BAA02g12230 | A02 | 5514398 | C | T | missense_variant | MODERATE | c.1204G>A|p.Ala402Thr |
S33 |
| 166106 | BAA02g12230 | A02 | 5514522 | G | A | synonymous_variant | LOW | c.1080C>T|p.Phe360Phe |
S235 |
| 166107 | BAA02g12240 | A02 | 5515703 | C | T | downstream_gene_variant | MODIFIER | c.*2264G>A| |
S199 |
| 166108 | BAA02g12230 | A02 | 5515825 | C | T | synonymous_variant | LOW | c.138G>A|p.Pro46Pro |
S221 |
| 166109 | BAA02g12230 | A02 | 5516929 | G | A | upstream_gene_variant | MODIFIER | c.-870C>T| |
S51 |
| 166110 | BAA02g12230 | A02 | 5517265 | G | A | upstream_gene_variant | MODIFIER | c.-1206C>T| |
S62 |
| 166111 | BAA02g12240 | A02 | 5518469 | G | A | missense_variant | MODERATE | c.1619C>T|p.Ser540Leu |
S259 |
| 166112 | BAA02g12240 | A02 | 5518631 | G | A | missense_variant | MODERATE | c.1549C>T|p.Pro517Ser |
S296 |
| 166113 | BAA02g12240 | A02 | 5518990 | G | A | missense_variant | MODERATE | c.1267C>T|p.Pro423Ser |
S19 |
| 166114 | BAA02g12240 | A02 | 5519481 | C | T | stop_gained | HIGH | c.948G>A|p.Trp316* |
S124 |
| 166115 | BAA02g12230 | A02 | 5519960 | G | A | upstream_gene_variant | MODIFIER | c.-3901C>T| |
S157 |
| 166116 | BAA02g12240 | A02 | 5520406 | G | A | missense_variant&splice_region_variant | MODERATE | c.197C>T|p.Ser66Phe |
S281 |
| 166117 | BAA02g12240 | A02 | 5520600 | G | A | synonymous_variant | LOW | c.105C>T|p.Tyr35Tyr |
S289 S290 |
| 166118 | BAA02g12240 | A02 | 5521485 | C | T | upstream_gene_variant | MODIFIER | c.-679G>A| |
S116 |
| 166119 | BAA02g12250 | A02 | 5522759 | G | A | missense_variant | MODERATE | c.127G>A|p.Glu43Lys |
S261 |
| 166120 | BAA02g12250 | A02 | 5523443 | C | T | missense_variant | MODERATE | c.239C>T|p.Pro80Leu |
S209 |
| 166121 | BAA02g12240 | A02 | 5523907 | C | T | upstream_gene_variant | MODIFIER | c.-3101G>A| |
S266 |
| 166122 | BAA02g12240 | A02 | 5524068 | G | A | upstream_gene_variant | MODIFIER | c.-3262C>T| |
S17 |
| 166123 | BAA02g12240 | A02 | 5524376 | G | A | upstream_gene_variant | MODIFIER | c.-3570C>T| |
S159 S243 |
| 166124 | BAA02g12270 | A02 | 5526968 | C | T | upstream_gene_variant | MODIFIER | c.-1188C>T| |
S167 |
| 166125 | BAA02g12260 | A02 | 5527134 | C | T | synonymous_variant | LOW | c.513C>T|p.Ser171Ser |
S115 |