| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g00540 | A08 | 366682 | G | A | downstream_gene_variant | MODIFIER | c.*4329C>T| |
S136 |
| 2 | BAA08g00540 | A08 | 366725 | G | A | downstream_gene_variant | MODIFIER | c.*4286C>T| |
S182 |
| 3 | BAA08g00540 | A08 | 366746 | C | T | downstream_gene_variant | MODIFIER | c.*4265G>A| |
S155 S211 |
| 4 | BAA08g00540 | A08 | 366752 | G | A | downstream_gene_variant | MODIFIER | c.*4259C>T| |
S298 |
| 5 | BAA08g00540 | A08 | 367098 | G | A | downstream_gene_variant | MODIFIER | c.*3913C>T| |
S129 |
| 6 | BAA08g00540 | A08 | 368080 | G | A | downstream_gene_variant | MODIFIER | c.*2931C>T| |
S40 S49 |
| 7 | BAA08g00540 | A08 | 368145 | C | T | downstream_gene_variant | MODIFIER | c.*2866G>A| |
S48 |
| 8 | BAA08g00540 | A08 | 369058 | G | A | downstream_gene_variant | MODIFIER | c.*1953C>T| |
S221 |
| 9 | BAA08g00540 | A08 | 369100 | C | T | downstream_gene_variant | MODIFIER | c.*1911G>A| |
S149 |
| 10 | BAA08g00540 | A08 | 369213 | C | T | downstream_gene_variant | MODIFIER | c.*1798G>A| |
S51 |
| 11 | BAA08g00540 | A08 | 369466 | C | T | downstream_gene_variant | MODIFIER | c.*1545G>A| |
S114 |
| 12 | BAA08g00540 | A08 | 369746 | C | T | downstream_gene_variant | MODIFIER | c.*1265G>A| |
S164 |
| 13 | BAA08g00540 | A08 | 369762 | C | T | downstream_gene_variant | MODIFIER | c.*1249G>A| |
S271 |
| 14 | BAA08g00540 | A08 | 369969 | C | A | downstream_gene_variant | MODIFIER | c.*1042G>T| |
S156 |
| 15 | BAA08g00540 | A08 | 371035 | C | T | synonymous_variant | LOW | c.1644G>A|p.Lys548Lys |
S209 |
| 16 | BAA08g00540 | A08 | 371065 | G | A | synonymous_variant | LOW | c.1614C>T|p.Leu538Leu |
S136 |
| 17 | BAA08g00540 | A08 | 371860 | G | A | missense_variant | MODERATE | c.923C>T|p.Ser308Phe |
S221 |
| 18 | BAA08g00540 | A08 | 372184 | C | T | missense_variant | MODERATE | c.599G>A|p.Gly200Glu |
S279 S64 |
| 19 | BAA08g00540 | A08 | 372230 | G | A | missense_variant | MODERATE | c.553C>T|p.Arg185Cys |
S223 |
| 20 | BAA08g00540 | A08 | 372353 | G | A | missense_variant | MODERATE | c.430C>T|p.Arg144Cys |
S58 |
| 21 | BAA08g00540 | A08 | 373654 | C | T | missense_variant | MODERATE | c.131G>A|p.Gly44Asp |
S134 |
| 22 | BAA08g00540 | A08 | 374396 | G | A | upstream_gene_variant | MODIFIER | c.-612C>T| |
S107 |
| 23 | BAA08g00540 | A08 | 374510 | G | A | upstream_gene_variant | MODIFIER | c.-726C>T| |
S188 S243 S298 S299 |
| 24 | BAA08g00540 | A08 | 374613 | G | A | upstream_gene_variant | MODIFIER | c.-829C>T| |
S16 |
| 25 | BAA08g00540 | A08 | 375468 | C | T | upstream_gene_variant | MODIFIER | c.-1684G>A| |
S275 |