| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 186551 | BAA02g23800 | A02 | 12978080 | G | A | downstream_gene_variant | MODIFIER | c.*2239C>T| |
S241 |
| 186552 | BAA02g23800 | A02 | 12978424 | C | T | downstream_gene_variant | MODIFIER | c.*1895G>A| |
S167 |
| 186553 | BAA02g23800 | A02 | 12981385 | C | T | missense_variant | MODERATE | c.374G>A|p.Gly125Asp |
S105 S106 |
| 186554 | BAA02g23810 | A02 | 12982110 | C | T | downstream_gene_variant | MODIFIER | c.*3455G>A| |
S252 |
| 186555 | BAA02g23810 | A02 | 12982471 | C | T | downstream_gene_variant | MODIFIER | c.*3094G>A| |
S224 |
| 186556 | BAA02g23800 | A02 | 12983427 | G | A | upstream_gene_variant | MODIFIER | c.-490C>T| |
S125 |
| 186557 | BAA02g23800 | A02 | 12983558 | C | T | upstream_gene_variant | MODIFIER | c.-621G>A| |
S65 |
| 186558 | BAA02g23800 | A02 | 12984991 | C | T | upstream_gene_variant | MODIFIER | c.-2054G>A| |
S11 |
| 186559 | BAA02g23810 | A02 | 12985915 | G | A | synonymous_variant | LOW | c.3309C>T|p.Ile1103Ile |
S251 |
| 186560 | BAA02g23810 | A02 | 12985919 | G | A | missense_variant | MODERATE | c.3305C>T|p.Pro1102Leu |
S153 S213 |
| 186561 | BAA02g23800 | A02 | 12986406 | C | T | upstream_gene_variant | MODIFIER | c.-3469G>A| |
S38 |
| 186562 | BAA02g23810 | A02 | 12987208 | C | T | missense_variant | MODERATE | c.2479G>A|p.Glu827Lys |
S286 |
| 186563 | BAA02g23810 | A02 | 12987649 | C | T | missense_variant | MODERATE | c.2038G>A|p.Glu680Lys |
S267 |
| 186564 | BAA02g23810 | A02 | 12987854 | G | A | synonymous_variant | LOW | c.1833C>T|p.Tyr611Tyr |
S98 |
| 186565 | BAA02g23800 | A02 | 12987931 | C | T | upstream_gene_variant | MODIFIER | c.-4994G>A| |
S284 |
| 186566 | BAA02g23810 | A02 | 12987961 | C | T | intron_variant | MODIFIER | c.1821+91G>A| |
S1 |
| 186567 | BAA02g23810 | A02 | 12988156 | C | T | missense_variant | MODERATE | c.1717G>A|p.Ala573Thr |
S158 |
| 186568 | BAA02g23810 | A02 | 12989719 | G | A | intron_variant | MODIFIER | c.970-311C>T| |
S62 |
| 186569 | BAA02g23810 | A02 | 12989844 | C | T | intron_variant | MODIFIER | c.970-436G>A| |
S174 |
| 186570 | BAA02g23810 | A02 | 12989958 | A | C | intron_variant | MODIFIER | c.970-550T>G| |
S138 |
| 186571 | BAA02g23820 | A02 | 12990622 | G | A | downstream_gene_variant | MODIFIER | c.*4658C>T| |
S293 |
| 186572 | BAA02g23810 | A02 | 12991044 | G | A | missense_variant | MODERATE | c.773C>T|p.Thr258Ile |
S61 |
| 186573 | BAA02g23820 | A02 | 12991575 | C | T | downstream_gene_variant | MODIFIER | c.*3705G>A| |
S40 |
| 186574 | BAA02g23810 | A02 | 12991829 | C | T | missense_variant | MODERATE | c.263G>A|p.Gly88Glu |
S250 |
| 186575 | BAA02g23810 | A02 | 12993200 | C | T | upstream_gene_variant | MODIFIER | c.-726G>A| |
S270 |