| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 14751 | BAA01g11440 | A01 | 5303797 | G | A | upstream_gene_variant | MODIFIER | c.-4874C>T| |
S228 |
| 14752 | BAA01g11450 | A01 | 5304332 | G | A | upstream_gene_variant | MODIFIER | c.-2367C>T| |
S74 |
| 14753 | BAA01g11450 | A01 | 5305274 | C | T | upstream_gene_variant | MODIFIER | c.-3309G>A| |
S226 |
| 14754 | BAA01g11450 | A01 | 5305310 | C | T | upstream_gene_variant | MODIFIER | c.-3345G>A| |
S249 |
| 14755 | BAA01g11450 | A01 | 5305425 | C | T | upstream_gene_variant | MODIFIER | c.-3460G>A| |
S301 S304 |
| 14756 | BAA01g11460 | A01 | 5306041 | G | A | synonymous_variant | LOW | c.417G>A|p.Arg139Arg |
S59 |
| 14757 | BAA01g11460 | A01 | 5306162 | G | A | missense_variant | MODERATE | c.538G>A|p.Gly180Arg |
S139 |
| 14758 | BAA01g11450 | A01 | 5306904 | C | T | upstream_gene_variant | MODIFIER | c.-4939G>A| |
S79 S84 |
| 14759 | BAA01g11460 | A01 | 5307917 | G | A | missense_variant | MODERATE | c.1586G>A|p.Cys529Tyr |
S263 |
| 14760 | BAA01g11460 | A01 | 5309325 | C | T | missense_variant | MODERATE | c.2323C>T|p.Pro775Ser |
S76 |
| 14761 | BAA01g11470 | A01 | 5309628 | G | A | downstream_gene_variant | MODIFIER | c.*2433C>T| |
S274 |
| 14762 | BAA01g11470 | A01 | 5309755 | C | T | downstream_gene_variant | MODIFIER | c.*2306G>A| |
S171 |
| 14763 | BAA01g11460 | A01 | 5310005 | C | T | synonymous_variant | LOW | c.2748C>T|p.Thr916Thr |
S203 |
| 14764 | BAA01g11470 | A01 | 5310548 | G | A | downstream_gene_variant | MODIFIER | c.*1513C>T| |
S157 S163 |
| 14765 | BAA01g11460 | A01 | 5311120 | C | T | synonymous_variant | LOW | c.3291C>T|p.Val1097Val |
S247 |
| 14766 | BAA01g11470 | A01 | 5312256 | C | T | splice_donor_variant&intron_variant | HIGH | c.2055+1G>A| |
S155 S211 |
| 14767 | BAA01g11470 | A01 | 5312763 | C | T | missense_variant | MODERATE | c.1724G>A|p.Gly575Glu |
S18 |
| 14768 | BAA01g11470 | A01 | 5313649 | G | A | missense_variant | MODERATE | c.1316C>T|p.Ser439Phe |
S275 |
| 14769 | BAA01g11460 | A01 | 5313842 | C | T | downstream_gene_variant | MODIFIER | c.*2587C>T| |
S71 |
| 14770 | BAA01g11470 | A01 | 5314028 | G | A | missense_variant | MODERATE | c.1028C>T|p.Pro343Leu |
S181 |
| 14771 | BAA01g11460 | A01 | 5314491 | C | T | downstream_gene_variant | MODIFIER | c.*3236C>T| |
S202 |
| 14772 | BAA01g11460 | A01 | 5314683 | G | A | downstream_gene_variant | MODIFIER | c.*3428G>A| |
S81 S85 |
| 14773 | BAA01g11470 | A01 | 5314978 | G | A | missense_variant | MODERATE | c.713C>T|p.Thr238Ile |
S165 |
| 14774 | BAA01g11460 | A01 | 5315057 | C | T | downstream_gene_variant | MODIFIER | c.*3802C>T| |
S260 S42 |
| 14775 | BAA01g11470 | A01 | 5316181 | G | A | synonymous_variant | LOW | c.345C>T|p.Ser115Ser |
S271 |