| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 81851 | BAA01g43250-BAA01g43260 | A01 | 28684381 | G | A | intergenic_region | MODIFIER | n.28684381G>A| |
S251 |
| 81852 | BAA01g43250-BAA01g43260 | A01 | 28685009 | T | C | intergenic_region | MODIFIER | n.28685009T>C| |
S11 S132 S136 S15 S163 S208 S216 S27 S275 S34 S48 S49 S53 S55 S66 S79 |
| 81853 | BAA01g43250-BAA01g43260 | A01 | 28687215 | C | A | intergenic_region | MODIFIER | n.28687215C>A| |
S196 S211 S275 S281 S287 S306 |
| 81854 | BAA01g43250-BAA01g43260 | A01 | 28688561 | C | T | intergenic_region | MODIFIER | n.28688561C>T| |
S74 |
| 81855 | BAA01g43260 | A01 | 28692601 | C | T | downstream_gene_variant | MODIFIER | c.*4297G>A| |
S157 |
| 81856 | BAA01g43260 | A01 | 28693583 | T | A | downstream_gene_variant | MODIFIER | c.*3315A>T| |
S123 |
| 81857 | BAA01g43260 | A01 | 28695456 | C | T | downstream_gene_variant | MODIFIER | c.*1442G>A| |
S120 |
| 81858 | BAA01g43260 | A01 | 28695795 | G | A | downstream_gene_variant | MODIFIER | c.*1103C>T| |
S262 S43 |
| 81859 | BAA01g43260 | A01 | 28696088 | C | T | downstream_gene_variant | MODIFIER | c.*810G>A| |
S23 |
| 81860 | BAA01g43260 | A01 | 28696526 | G | A | downstream_gene_variant | MODIFIER | c.*372C>T| |
S87 |
| 81861 | BAA01g43260 | A01 | 28696695 | C | T | downstream_gene_variant | MODIFIER | c.*203G>A| |
S273 |
| 81862 | BAA01g43260 | A01 | 28696772 | C | T | downstream_gene_variant | MODIFIER | c.*126G>A| |
S274 |
| 81863 | BAA01g43270 | A01 | 28697759 | G | A | downstream_gene_variant | MODIFIER | c.*669C>T| |
S84 S93 |
| 81864 | BAA01g43270 | A01 | 28698532 | C | T | missense_variant | MODERATE | c.691G>A|p.Val231Ile |
S233 |
| 81865 | BAA01g43270 | A01 | 28698718 | G | A | missense_variant | MODERATE | c.505C>T|p.Leu169Phe |
S265 |
| 81866 | BAA01g43270 | A01 | 28699117 | G | A | missense_variant | MODERATE | c.106C>T|p.His36Tyr |
S278 |
| 81867 | BAA01g43270 | A01 | 28699118 | G | A | synonymous_variant | LOW | c.105C>T|p.Pro35Pro |
S225 |
| 81868 | BAA01g43260 | A01 | 28702094 | G | A | upstream_gene_variant | MODIFIER | c.-3956C>T| |
S140 |
| 81869 | BAA01g43280 | A01 | 28706276 | C | T | missense_variant | MODERATE | c.949C>T|p.Leu317Phe |
S204 |
| 81870 | BAA01g43280 | A01 | 28707413 | C | T | downstream_gene_variant | MODIFIER | c.*200C>T| |
S97 |
| 81871 | BAA01g43310 | A01 | 28708350 | C | T | upstream_gene_variant | MODIFIER | c.-4147C>T| |
S261 |
| 81872 | BAA01g43310 | A01 | 28708423 | C | T | upstream_gene_variant | MODIFIER | c.-4074C>T| |
S65 |
| 81873 | BAA01g43310 | A01 | 28708682 | C | T | upstream_gene_variant | MODIFIER | c.-3815C>T| |
S89 |
| 81874 | BAA01g43300 | A01 | 28710530 | C | T | synonymous_variant | LOW | c.870G>A|p.Thr290Thr |
S162 |
| 81875 | BAA01g43300 | A01 | 28710542 | C | T | synonymous_variant | LOW | c.858G>A|p.Val286Val |
S75 S81 |