| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 158901 | BAA02g06410 | A02 | 2720809 | G | A | synonymous_variant | LOW | c.2814G>A|p.Val938Val |
S169 |
| 158902 | BAA02g06410 | A02 | 2721104 | G | A | missense_variant | MODERATE | c.3109G>A|p.Asp1037Asn |
S48 |
| 158903 | BAA02g06420 | A02 | 2721530 | C | T | upstream_gene_variant | MODIFIER | c.-2907C>T| |
S38 |
| 158904 | BAA02g06420 | A02 | 2723982 | C | T | upstream_gene_variant | MODIFIER | c.-455C>T| |
S242 |
| 158905 | BAA02g06410 | A02 | 2724622 | C | T | downstream_gene_variant | MODIFIER | c.*3135C>T| |
S194 |
| 158906 | BAA02g06420 | A02 | 2724970 | C | T | missense_variant | MODERATE | c.374C>T|p.Thr125Ile |
S97 |
| 158907 | BAA02g06410 | A02 | 2725336 | G | A | downstream_gene_variant | MODIFIER | c.*3849G>A| |
S291 |
| 158908 | BAA02g06410 | A02 | 2726087 | G | A | downstream_gene_variant | MODIFIER | c.*4600G>A| |
S177 |
| 158909 | BAA02g06410 | A02 | 2726317 | G | A | downstream_gene_variant | MODIFIER | c.*4830G>A| |
S239 |
| 158910 | BAA02g06420 | A02 | 2727116 | G | A | downstream_gene_variant | MODIFIER | c.*1329G>A| |
S133 |
| 158911 | BAA02g06420 | A02 | 2727536 | G | A | downstream_gene_variant | MODIFIER | c.*1749G>A| |
S28 |
| 158912 | BAA02g06430 | A02 | 2729624 | C | T | missense_variant | MODERATE | c.1324G>A|p.Glu442Lys |
S200 |
| 158913 | BAA02g06430 | A02 | 2730753 | G | A | stop_gained | HIGH | c.859C>T|p.Gln287* |
S158 |
| 158914 | BAA02g06430 | A02 | 2731275 | C | T | missense_variant | MODERATE | c.337G>A|p.Glu113Lys |
S242 |
| 158915 | BAA02g06430 | A02 | 2731333 | C | T | synonymous_variant | LOW | c.279G>A|p.Ala93Ala |
S233 |
| 158916 | BAA02g06430 | A02 | 2731548 | G | A | missense_variant | MODERATE | c.64C>T|p.Leu22Phe |
S25 |
| 158917 | BAA02g06430 | A02 | 2732152 | G | A | upstream_gene_variant | MODIFIER | c.-541C>T| |
S20 |
| 158918 | BAA02g06430 | A02 | 2732626 | C | T | upstream_gene_variant | MODIFIER | c.-1015G>A| |
S301 S304 |
| 158919 | BAA02g06440 | A02 | 2733055 | G | A | synonymous_variant | LOW | c.417G>A|p.Leu139Leu |
S264 |
| 158920 | BAA02g06440 | A02 | 2733539 | C | T | missense_variant | MODERATE | c.901C>T|p.Pro301Ser |
S255 |
| 158921 | BAA02g06430 | A02 | 2734648 | G | A | upstream_gene_variant | MODIFIER | c.-3037C>T| |
S52 |
| 158922 | BAA02g06430 | A02 | 2734835 | G | A | upstream_gene_variant | MODIFIER | c.-3224C>T| |
S187 |
| 158923 | BAA02g06430 | A02 | 2734892 | C | T | upstream_gene_variant | MODIFIER | c.-3281G>A| |
S167 |
| 158924 | BAA02g06430 | A02 | 2735022 | G | A | upstream_gene_variant | MODIFIER | c.-3411C>T| |
S143 |
| 158925 | BAA02g06450 | A02 | 2735825 | C | T | missense_variant | MODERATE | c.2629G>A|p.Asp877Asn |
S278 |