| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 78801 | BAA01g41450 | A01 | 27549691 | C | A | upstream_gene_variant | MODIFIER | c.-3206C>A| |
S228 |
| 78802 | BAA01g41450 | A01 | 27549697 | G | A | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S113 |
| 78803 | BAA01g41450 | A01 | 27550234 | C | T | upstream_gene_variant | MODIFIER | c.-2663C>T| |
S210 S225 |
| 78804 | BAA01g41450 | A01 | 27552049 | G | A | upstream_gene_variant | MODIFIER | c.-848G>A| |
S86 |
| 78805 | BAA01g41440 | A01 | 27553381 | G | A | downstream_gene_variant | MODIFIER | c.*4668G>A| |
S267 |
| 78806 | BAA01g41450 | A01 | 27554222 | G | A | synonymous_variant | LOW | c.975G>A|p.Glu325Glu |
S191 |
| 78807 | BAA01g41450 | A01 | 27554710 | C | T | downstream_gene_variant | MODIFIER | c.*119C>T| |
S260 |
| 78808 | BAA01g41450 | A01 | 27554840 | C | T | downstream_gene_variant | MODIFIER | c.*249C>T| |
S205 |
| 78809 | BAA01g41460 | A01 | 27555392 | G | A | missense_variant | MODERATE | c.1625C>T|p.Ala542Val |
S71 |
| 78810 | BAA01g41460 | A01 | 27556065 | G | A | missense_variant | MODERATE | c.1325C>T|p.Ala442Val |
S104 |
| 78811 | BAA01g41460 | A01 | 27556230 | C | T | splice_region_variant&intron_variant | LOW | c.1248+3G>A| |
S210 S225 |
| 78812 | BAA01g41460 | A01 | 27556756 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.913-1G>A| |
S183 |
| 78813 | BAA01g41470 | A01 | 27557190 | G | A | upstream_gene_variant | MODIFIER | c.-3067G>A| |
S15 S3 |
| 78814 | BAA01g41470 | A01 | 27557504 | G | A | upstream_gene_variant | MODIFIER | c.-2753G>A| |
S202 |
| 78815 | BAA01g41460 | A01 | 27558455 | C | T | missense_variant | MODERATE | c.223G>A|p.Val75Ile |
S251 |
| 78816 | BAA01g41460 | A01 | 27559064 | C | T | upstream_gene_variant | MODIFIER | c.-307G>A| |
S269 |
| 78817 | BAA01g41460 | A01 | 27559303 | G | A | upstream_gene_variant | MODIFIER | c.-546C>T| |
S306 |
| 78818 | BAA01g41460 | A01 | 27559467 | G | A | upstream_gene_variant | MODIFIER | c.-710C>T| |
S123 |
| 78819 | BAA01g41460 | A01 | 27561866 | C | T | upstream_gene_variant | MODIFIER | c.-3109G>A| |
S118 |
| 78820 | BAA01g41480 | A01 | 27562320 | C | T | synonymous_variant | LOW | c.246C>T|p.Leu82Leu |
S100 |
| 78821 | BAA01g41480 | A01 | 27562493 | G | A | missense_variant | MODERATE | c.419G>A|p.Arg140Lys |
S33 |
| 78822 | BAA01g41460 | A01 | 27562771 | G | A | upstream_gene_variant | MODIFIER | c.-4014C>T| |
S190 |
| 78823 | BAA01g41490 | A01 | 27563712 | C | T | stop_gained | HIGH | c.1254G>A|p.Trp418* |
S64 |
| 78824 | BAA01g41490 | A01 | 27564634 | C | T | synonymous_variant | LOW | c.984G>A|p.Glu328Glu |
S54 |
| 78825 | BAA01g41500 | A01 | 27565656 | C | T | upstream_gene_variant | MODIFIER | c.-3666C>T| |
S62 |