| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 161101 | BAA02g08250 | A02 | 3535957 | G | A | stop_gained | HIGH | c.1149G>A|p.Trp383* |
S197 |
| 161102 | BAA02g08250 | A02 | 3535994 | G | A | missense_variant | MODERATE | c.1186G>A|p.Val396Met |
S269 |
| 161103 | BAA02g08240 | A02 | 3536486 | C | T | upstream_gene_variant | MODIFIER | c.-3663G>A| |
S268 |
| 161104 | BAA02g08240 | A02 | 3536673 | G | A | upstream_gene_variant | MODIFIER | c.-3850C>T| |
S67 |
| 161105 | BAA02g08260 | A02 | 3537384 | C | T | synonymous_variant | LOW | c.537C>T|p.Tyr179Tyr |
S121 |
| 161106 | BAA02g08260 | A02 | 3537990 | G | A | synonymous_variant | LOW | c.1143G>A|p.Thr381Thr |
S269 |
| 161107 | BAA02g08270 | A02 | 3538594 | G | A | upstream_gene_variant | MODIFIER | c.-452G>A| |
S289 S290 |
| 161108 | BAA02g08280 | A02 | 3540229 | G | A | upstream_gene_variant | MODIFIER | c.-4000G>A| |
S269 |
| 161109 | BAA02g08280 | A02 | 3541382 | C | T | upstream_gene_variant | MODIFIER | c.-2847C>T| |
S130 |
| 161110 | BAA02g08280 | A02 | 3541534 | C | T | upstream_gene_variant | MODIFIER | c.-2695C>T| |
S262 |
| 161111 | BAA02g08280 | A02 | 3542827 | C | T | upstream_gene_variant | MODIFIER | c.-1402C>T| |
S219 |
| 161112 | BAA02g08270 | A02 | 3544311 | G | A | downstream_gene_variant | MODIFIER | c.*3350G>A| |
S133 |
| 161113 | BAA02g08280 | A02 | 3544406 | C | T | missense_variant | MODERATE | c.91C>T|p.Pro31Ser |
S46 |
| 161114 | BAA02g08270 | A02 | 3544812 | C | T | downstream_gene_variant | MODIFIER | c.*3851C>T| |
S136 |
| 161115 | BAA02g08270 | A02 | 3545042 | G | A | downstream_gene_variant | MODIFIER | c.*4081G>A| |
S19 |
| 161116 | BAA02g08280 | A02 | 3545712 | C | T | missense_variant | MODERATE | c.947C>T|p.Pro316Leu |
S13 |
| 161117 | BAA02g08280 | A02 | 3546244 | C | T | missense_variant | MODERATE | c.1235C>T|p.Ser412Leu |
S180 |
| 161118 | BAA02g08280 | A02 | 3546390 | C | T | downstream_gene_variant | MODIFIER | c.*79C>T| |
S278 |
| 161119 | BAA02g08290 | A02 | 3548568 | G | A | synonymous_variant | LOW | c.753C>T|p.Phe251Phe |
S165 |
| 161120 | BAA02g08290 | A02 | 3549642 | G | A | upstream_gene_variant | MODIFIER | c.-322C>T| |
S223 |
| 161121 | BAA02g08290 | A02 | 3552136 | C | T | upstream_gene_variant | MODIFIER | c.-2816G>A| |
S224 |
| 161122 | BAA02g08300 | A02 | 3552473 | G | A | stop_gained | HIGH | c.705G>A|p.Trp235* |
S163 |
| 161123 | BAA02g08300 | A02 | 3552588 | G | A | missense_variant | MODERATE | c.820G>A|p.Val274Ile |
S98 |
| 161124 | BAA02g08300 | A02 | 3552755 | G | A | synonymous_variant | LOW | c.987G>A|p.Ser329Ser |
S125 |
| 161125 | BAA02g08300 | A02 | 3554544 | G | A | downstream_gene_variant | MODIFIER | c.*1594G>A| |
S105 S106 |