| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 169101 | BAA02g14260 | A02 | 6671328 | C | T | missense_variant | MODERATE | c.1183G>A|p.Gly395Ser |
S71 |
| 169102 | BAA02g14250 | A02 | 6671483 | C | T | downstream_gene_variant | MODIFIER | c.*3646C>T| |
S272 |
| 169103 | BAA02g14260 | A02 | 6672124 | C | T | missense_variant | MODERATE | c.631G>A|p.Asp211Asn |
S272 |
| 169104 | BAA02g14260 | A02 | 6672655 | C | T | missense_variant | MODERATE | c.100G>A|p.Ala34Thr |
S206 S26 |
| 169105 | BAA02g14260 | A02 | 6673249 | G | A | upstream_gene_variant | MODIFIER | c.-495C>T| |
S190 |
| 169106 | BAA02g14260 | A02 | 6673581 | G | A | upstream_gene_variant | MODIFIER | c.-827C>T| |
S192 |
| 169107 | BAA02g14260 | A02 | 6673720 | C | T | upstream_gene_variant | MODIFIER | c.-966G>A| |
S182 |
| 169108 | BAA02g14260 | A02 | 6674002 | G | A | upstream_gene_variant | MODIFIER | c.-1248C>T| |
S280 |
| 169109 | BAA02g14260 | A02 | 6675022 | G | A | upstream_gene_variant | MODIFIER | c.-2268C>T| |
S202 |
| 169110 | BAA02g14270 | A02 | 6677098 | G | A | missense_variant | MODERATE | c.386C>T|p.Pro129Leu |
S82 S92 |
| 169111 | BAA02g14260 | A02 | 6677392 | G | A | upstream_gene_variant | MODIFIER | c.-4638C>T| |
S264 S293 |
| 169112 | BAA02g14270 | A02 | 6677961 | C | T | upstream_gene_variant | MODIFIER | c.-243G>A| |
S92 |
| 169113 | BAA02g14270 | A02 | 6679105 | G | A | upstream_gene_variant | MODIFIER | c.-1387C>T| |
S282 |
| 169114 | BAA02g14270 | A02 | 6680141 | G | A | upstream_gene_variant | MODIFIER | c.-2423C>T| |
S256 |
| 169115 | BAA02g14270 | A02 | 6680217 | C | G | upstream_gene_variant | MODIFIER | c.-2499G>C| |
S108 |
| 169116 | BAA02g14270 | A02 | 6680416 | T | A | upstream_gene_variant | MODIFIER | c.-2698A>T| |
S257 |
| 169117 | BAA02g14270-BAA02g14280 | A02 | 6682947 | C | T | intergenic_region | MODIFIER | n.6682947C>T| |
S283 |
| 169118 | BAA02g14280 | A02 | 6686407 | C | T | downstream_gene_variant | MODIFIER | c.*2707G>A| |
S120 |
| 169119 | BAA02g14280 | A02 | 6687201 | C | T | downstream_gene_variant | MODIFIER | c.*1913G>A| |
S183 |
| 169120 | BAA02g14290 | A02 | 6687837 | C | T | upstream_gene_variant | MODIFIER | c.-4950C>T| |
S179 |
| 169121 | BAA02g14290 | A02 | 6690264 | G | A | upstream_gene_variant | MODIFIER | c.-2523G>A| |
S132 S137 S215 |
| 169122 | BAA02g14280 | A02 | 6691502 | A | T | upstream_gene_variant | MODIFIER | c.-520T>A| |
S266 |
| 169123 | BAA02g14280 | A02 | 6692057 | C | T | upstream_gene_variant | MODIFIER | c.-1075G>A| |
S25 |
| 169124 | BAA02g14290 | A02 | 6693335 | G | A | missense_variant | MODERATE | c.469G>A|p.Asp157Asn |
S2 |
| 169125 | BAA02g14290 | A02 | 6693758 | C | T | stop_gained | HIGH | c.706C>T|p.Gln236* |
S32 |