| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 170651 | BAA02g15160 | A02 | 7277484 | C | T | missense_variant | MODERATE | c.433C>T|p.Leu145Phe |
S115 |
| 170652 | BAA02g15150 | A02 | 7280099 | G | A | upstream_gene_variant | MODIFIER | c.-4950C>T| |
S264 |
| 170653 | BAA02g15150 | A02 | 7280115 | C | T | upstream_gene_variant | MODIFIER | c.-4966G>A| |
S286 |
| 170654 | BAA02g15170 | A02 | 7280287 | C | T | upstream_gene_variant | MODIFIER | c.-1638C>T| |
S99 |
| 170655 | BAA02g15170 | A02 | 7280692 | C | T | upstream_gene_variant | MODIFIER | c.-1233C>T| |
S244 |
| 170656 | BAA02g15170 | A02 | 7281112 | G | A | upstream_gene_variant | MODIFIER | c.-813G>A| |
S170 |
| 170657 | BAA02g15170 | A02 | 7281875 | G | A | upstream_gene_variant | MODIFIER | c.-50G>A| |
S92 |
| 170658 | BAA02g15170 | A02 | 7282251 | C | T | synonymous_variant | LOW | c.261C>T|p.Arg87Arg |
S262 |
| 170659 | BAA02g15170 | A02 | 7283398 | C | T | missense_variant | MODERATE | c.836C>T|p.Ser279Phe |
S84 S93 |
| 170660 | BAA02g15170 | A02 | 7283765 | G | A | missense_variant&splice_region_variant | MODERATE | c.919G>A|p.Glu307Lys |
S4 |
| 170661 | BAA02g15180 | A02 | 7283866 | C | T | upstream_gene_variant | MODIFIER | c.-787C>T| |
S104 |
| 170662 | BAA02g15190 | A02 | 7284796 | G | A | upstream_gene_variant | MODIFIER | c.-966G>A| |
S187 |
| 170663 | BAA02g15170 | A02 | 7286261 | G | A | downstream_gene_variant | MODIFIER | c.*2247G>A| |
S188 |
| 170664 | BAA02g15190 | A02 | 7287656 | G | A | missense_variant | MODERATE | c.1139G>A|p.Gly380Asp |
S53 |
| 170665 | BAA02g15190 | A02 | 7287905 | C | T | missense_variant | MODERATE | c.1313C>T|p.Ser438Phe |
S84 S93 |
| 170666 | BAA02g15190 | A02 | 7288190 | C | T | missense_variant | MODERATE | c.1522C>T|p.His508Tyr |
S163 |
| 170667 | BAA02g15190 | A02 | 7288497 | G | A | missense_variant | MODERATE | c.1654G>A|p.Glu552Lys |
S162 |
| 170668 | BAA02g15200 | A02 | 7291736 | G | A | missense_variant | MODERATE | c.103C>T|p.Leu35Phe |
S113 |
| 170669 | BAA02g15200 | A02 | 7291916 | C | T | upstream_gene_variant | MODIFIER | c.-78G>A| |
S32 |
| 170670 | BAA02g15200 | A02 | 7292141 | G | T | upstream_gene_variant | MODIFIER | c.-303C>A| |
S221 |
| 170671 | BAA02g15200 | A02 | 7292171 | G | A | upstream_gene_variant | MODIFIER | c.-333C>T| |
S228 |
| 170672 | BAA02g15200 | A02 | 7292617 | C | T | upstream_gene_variant | MODIFIER | c.-779G>A| |
S54 |
| 170673 | BAA02g15200 | A02 | 7292668 | C | T | upstream_gene_variant | MODIFIER | c.-830G>A| |
S250 |
| 170674 | BAA02g15200 | A02 | 7294198 | G | A | upstream_gene_variant | MODIFIER | c.-2360C>T| |
S157 |
| 170675 | BAA02g15220 | A02 | 7294446 | G | A | missense_variant | MODERATE | c.737C>T|p.Thr246Ile |
S69 |