| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g02900 | A08 | 2058997 | C | T | missense_variant | MODERATE | c.808G>A|p.Val270Met |
S66 |
| 2 | BAA08g02900 | A08 | 2059035 | G | A | missense_variant | MODERATE | c.770C>T|p.Pro257Leu |
S18 |
| 3 | BAA08g02900 | A08 | 2059236 | C | T | missense_variant | MODERATE | c.569G>A|p.Arg190His |
S206 S26 |
| 4 | BAA08g02900 | A08 | 2060655 | G | A | missense_variant | MODERATE | c.559C>T|p.Pro187Ser |
S306 S308 |
| 5 | BAA08g02900 | A08 | 2060816 | C | T | missense_variant | MODERATE | c.398G>A|p.Gly133Glu |
S205 |
| 6 | BAA08g02900 | A08 | 2061577 | C | T | upstream_gene_variant | MODIFIER | c.-364G>A| |
S70 |
| 7 | BAA08g02900 | A08 | 2062944 | C | T | upstream_gene_variant | MODIFIER | c.-1731G>A| |
S235 |
| 8 | BAA08g02900 | A08 | 2063372 | C | T | upstream_gene_variant | MODIFIER | c.-2159G>A| |
S53 |
| 9 | BAA08g02900 | A08 | 2063697 | C | T | upstream_gene_variant | MODIFIER | c.-2484G>A| |
S283 |
| 10 | BAA08g02900 | A08 | 2063727 | G | A | upstream_gene_variant | MODIFIER | c.-2514C>T| |
S262 |
| 11 | BAA08g02900 | A08 | 2063894 | C | T | upstream_gene_variant | MODIFIER | c.-2681G>A| |
S104 S52 |
| 12 | BAA08g02900 | A08 | 2064525 | C | T | upstream_gene_variant | MODIFIER | c.-3312G>A| |
S12 |
| 13 | BAA08g02900 | A08 | 2064619 | G | A | upstream_gene_variant | MODIFIER | c.-3406C>T| |
S264 |
| 14 | BAA08g02900 | A08 | 2064684 | G | A | upstream_gene_variant | MODIFIER | c.-3471C>T| |
S148 S210 |
| 15 | BAA08g02900 | A08 | 2065286 | G | A | upstream_gene_variant | MODIFIER | c.-4073C>T| |
S200 S274 S303 |