| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178701 | BAA02g19530 | A02 | 10141503 | C | T | missense_variant | MODERATE | c.431C>T|p.Pro144Leu |
S246 |
| 178702 | BAA02g19530 | A02 | 10143996 | C | T | downstream_gene_variant | MODIFIER | c.*2066C>T| |
S268 |
| 178703 | BAA02g19540 | A02 | 10144763 | A | T | upstream_gene_variant | MODIFIER | c.-4668A>T| |
S104 S52 |
| 178704 | BAA02g19540 | A02 | 10145214 | C | T | upstream_gene_variant | MODIFIER | c.-4217C>T| |
S201 |
| 178705 | BAA02g19540 | A02 | 10145721 | C | T | upstream_gene_variant | MODIFIER | c.-3710C>T| |
S289 S290 |
| 178706 | BAA02g19540 | A02 | 10145750 | C | T | upstream_gene_variant | MODIFIER | c.-3681C>T| |
S185 |
| 178707 | BAA02g19540 | A02 | 10145775 | C | T | upstream_gene_variant | MODIFIER | c.-3656C>T| |
S202 |
| 178708 | BAA02g19540 | A02 | 10145885 | C | T | upstream_gene_variant | MODIFIER | c.-3546C>T| |
S262 |
| 178709 | BAA02g19540 | A02 | 10145887 | C | T | upstream_gene_variant | MODIFIER | c.-3544C>T| |
S46 |
| 178710 | BAA02g19540 | A02 | 10145921 | C | T | upstream_gene_variant | MODIFIER | c.-3510C>T| |
S164 |
| 178711 | BAA02g19540 | A02 | 10147112 | C | T | upstream_gene_variant | MODIFIER | c.-2319C>T| |
S238 |
| 178712 | BAA02g19540 | A02 | 10147807 | C | T | upstream_gene_variant | MODIFIER | c.-1624C>T| |
S270 |
| 178713 | BAA02g19540 | A02 | 10148219 | G | A | upstream_gene_variant | MODIFIER | c.-1212G>A| |
S184 |
| 178714 | BAA02g19540 | A02 | 10148396 | C | T | upstream_gene_variant | MODIFIER | c.-1035C>T| |
S94 |
| 178715 | BAA02g19540 | A02 | 10148906 | C | T | upstream_gene_variant | MODIFIER | c.-525C>T| |
S112 |
| 178716 | BAA02g19540 | A02 | 10149042 | G | A | upstream_gene_variant | MODIFIER | c.-389G>A| |
S247 |
| 178717 | BAA02g19540 | A02 | 10150092 | G | A | missense_variant | MODERATE | c.662G>A|p.Gly221Glu |
S206 S26 |
| 178718 | BAA02g19540 | A02 | 10150120 | C | T | synonymous_variant | LOW | c.690C>T|p.Val230Val |
S241 |
| 178719 | BAA02g19540 | A02 | 10150253 | G | A | downstream_gene_variant | MODIFIER | c.*31G>A| |
S48 |
| 178720 | BAA02g19540 | A02 | 10150473 | G | A | downstream_gene_variant | MODIFIER | c.*251G>A| |
S45 |
| 178721 | BAA02g19540 | A02 | 10151303 | C | T | downstream_gene_variant | MODIFIER | c.*1081C>T| |
S40 S49 |
| 178722 | BAA02g19540 | A02 | 10152651 | C | T | downstream_gene_variant | MODIFIER | c.*2429C>T| |
S2 |
| 178723 | BAA02g19540 | A02 | 10154460 | G | A | downstream_gene_variant | MODIFIER | c.*4238G>A| |
S173 |
| 178724 | BAA02g19540 | A02 | 10155132 | G | T | downstream_gene_variant | MODIFIER | c.*4910G>T| |
S153 S213 |
| 178725 | BAA02g19540 | A02 | 10155178 | C | T | downstream_gene_variant | MODIFIER | c.*4956C>T| |
S246 |