| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 75101 | BAA01g39550 | A01 | 26297137 | C | T | upstream_gene_variant | MODIFIER | c.-295G>A| |
S281 |
| 75102 | BAA01g39550 | A01 | 26297984 | G | A | upstream_gene_variant | MODIFIER | c.-1142C>T| |
S286 |
| 75103 | BAA01g39550 | A01 | 26298545 | G | A | upstream_gene_variant | MODIFIER | c.-1703C>T| |
S103 |
| 75104 | BAA01g39550 | A01 | 26298725 | C | T | upstream_gene_variant | MODIFIER | c.-1883G>A| |
S82 S92 |
| 75105 | BAA01g39550 | A01 | 26299587 | G | A | upstream_gene_variant | MODIFIER | c.-2745C>T| |
S197 |
| 75106 | BAA01g39550 | A01 | 26299762 | C | T | upstream_gene_variant | MODIFIER | c.-2920G>A| |
S192 |
| 75107 | BAA01g39550 | A01 | 26300931 | C | T | upstream_gene_variant | MODIFIER | c.-4089G>A| |
S51 S85 |
| 75108 | BAA01g39550 | A01 | 26301193 | C | T | upstream_gene_variant | MODIFIER | c.-4351G>A| |
S133 |
| 75109 | BAA01g39560 | A01 | 26302470 | C | T | upstream_gene_variant | MODIFIER | c.-631C>T| |
S134 |
| 75110 | BAA01g39560 | A01 | 26303379 | C | T | missense_variant | MODERATE | c.191C>T|p.Ser64Phe |
S236 |
| 75111 | BAA01g39560 | A01 | 26303451 | C | T | missense_variant | MODERATE | c.263C>T|p.Thr88Ile |
S148 S210 S30 S31 |
| 75112 | BAA01g39560 | A01 | 26303609 | G | A | missense_variant | MODERATE | c.350G>A|p.Cys117Tyr |
S70 |
| 75113 | BAA01g39560 | A01 | 26305314 | G | A | missense_variant | MODERATE | c.1144G>A|p.Asp382Asn |
S225 S73 |
| 75114 | BAA01g39560 | A01 | 26306363 | G | A | missense_variant | MODERATE | c.1747G>A|p.Ala583Thr |
S278 |
| 75115 | BAA01g39570 | A01 | 26307452 | C | T | upstream_gene_variant | MODIFIER | c.-1598C>T| |
S303 |
| 75116 | BAA01g39570 | A01 | 26307725 | G | A | upstream_gene_variant | MODIFIER | c.-1325G>A| |
S123 |
| 75117 | BAA01g39570 | A01 | 26307882 | C | T | upstream_gene_variant | MODIFIER | c.-1168C>T| |
S210 S225 |
| 75118 | BAA01g39570 | A01 | 26307892 | C | T | upstream_gene_variant | MODIFIER | c.-1158C>T| |
S23 |
| 75119 | BAA01g39570 | A01 | 26307932 | G | A | upstream_gene_variant | MODIFIER | c.-1118G>A| |
S281 |
| 75120 | BAA01g39590 | A01 | 26310846 | G | A | upstream_gene_variant | MODIFIER | c.-2529G>A| |
S20 S238 |
| 75121 | BAA01g39590 | A01 | 26311563 | G | A | upstream_gene_variant | MODIFIER | c.-1812G>A| |
S20 |
| 75122 | BAA01g39580 | A01 | 26311771 | G | A | missense_variant | MODERATE | c.122C>T|p.Ala41Val |
S252 |
| 75123 | BAA01g39580 | A01 | 26312282 | G | A | upstream_gene_variant | MODIFIER | c.-303C>T| |
S262 |
| 75124 | BAA01g39580 | A01 | 26313299 | C | T | upstream_gene_variant | MODIFIER | c.-1320G>A| |
S150 |
| 75125 | BAA01g39590 | A01 | 26313494 | G | A | synonymous_variant | LOW | c.120G>A|p.Val40Val |
S135 |