| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156751 | BAA02g04690 | A02 | 2035848 | G | A | synonymous_variant | LOW | c.522G>A|p.Ser174Ser |
S48 |
| 156752 | BAA02g04680 | A02 | 2036326 | C | T | upstream_gene_variant | MODIFIER | c.-3893G>A| |
S65 |
| 156753 | BAA02g04680 | A02 | 2036395 | C | T | upstream_gene_variant | MODIFIER | c.-3962G>A| |
S195 |
| 156754 | BAA02g04690 | A02 | 2037328 | C | T | synonymous_variant | LOW | c.1090C>T|p.Leu364Leu |
S152 |
| 156755 | BAA02g04690 | A02 | 2039202 | C | T | downstream_gene_variant | MODIFIER | c.*1593C>T| |
S252 |
| 156756 | BAA02g04690 | A02 | 2040230 | C | T | downstream_gene_variant | MODIFIER | c.*2621C>T| |
S19 |
| 156757 | BAA02g04720 | A02 | 2042636 | G | A | upstream_gene_variant | MODIFIER | c.-4362G>A| |
S96 |
| 156758 | BAA02g04720 | A02 | 2042834 | G | A | upstream_gene_variant | MODIFIER | c.-4164G>A| |
S264 |
| 156759 | BAA02g04710 | A02 | 2043729 | G | A | missense_variant | MODERATE | c.784C>T|p.Pro262Ser |
S188 |
| 156760 | BAA02g04710 | A02 | 2044014 | C | T | missense_variant | MODERATE | c.499G>A|p.Val167Met |
S88 |
| 156761 | BAA02g04710 | A02 | 2044705 | G | A | synonymous_variant | LOW | c.132C>T|p.Ser44Ser |
S17 |
| 156762 | BAA02g04710 | A02 | 2044713 | G | A | missense_variant | MODERATE | c.124C>T|p.Leu42Phe |
S106 S68 |
| 156763 | BAA02g04710 | A02 | 2045076 | C | T | upstream_gene_variant | MODIFIER | c.-240G>A| |
S71 |
| 156764 | BAA02g04710 | A02 | 2045250 | C | T | upstream_gene_variant | MODIFIER | c.-414G>A| |
S150 |
| 156765 | BAA02g04710 | A02 | 2045380 | C | T | upstream_gene_variant | MODIFIER | c.-544G>A| |
S117 |
| 156766 | BAA02g04710 | A02 | 2046821 | G | A | upstream_gene_variant | MODIFIER | c.-1985C>T| |
S291 |
| 156767 | BAA02g04720 | A02 | 2047078 | G | A | synonymous_variant | LOW | c.81G>A|p.Leu27Leu |
S114 |
| 156768 | BAA02g04710 | A02 | 2049141 | G | A | upstream_gene_variant | MODIFIER | c.-4305C>T| |
S156 |
| 156769 | BAA02g04710 | A02 | 2049165 | G | A | upstream_gene_variant | MODIFIER | c.-4329C>T| |
S122 |
| 156770 | BAA02g04730 | A02 | 2049603 | C | T | missense_variant | MODERATE | c.1015G>A|p.Asp339Asn |
S255 |
| 156771 | BAA02g04730 | A02 | 2049866 | G | A | missense_variant | MODERATE | c.752C>T|p.Thr251Ile |
S192 |
| 156772 | BAA02g04720 | A02 | 2050503 | G | A | downstream_gene_variant | MODIFIER | c.*3149G>A| |
S67 |
| 156773 | BAA02g04730 | A02 | 2051377 | C | T | missense_variant | MODERATE | c.364G>A|p.Glu122Lys |
S103 |
| 156774 | BAA02g04730 | A02 | 2051470 | C | T | missense_variant | MODERATE | c.271G>A|p.Gly91Arg |
S243 S299 |
| 156775 | BAA02g04730 | A02 | 2052548 | G | A | upstream_gene_variant | MODIFIER | c.-808C>T| |
S273 |