Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66060 | A03 | 40346643 | G | A | upstream_gene_variant | MODIFIER | c.-553G>A| |
S135 |
2 | BAA03g66060 | A03 | 40347258 | G | A | synonymous_variant | LOW | c.63G>A|p.Arg21Arg |
S138 |
3 | BAA03g66060 | A03 | 40347507 | G | A | synonymous_variant | LOW | c.312G>A|p.Glu104Glu |
S286 |
4 | BAA03g66060 | A03 | 40348061 | G | A | missense_variant | MODERATE | c.866G>A|p.Gly289Glu |
S81 S85 |
5 | BAA03g66060 | A03 | 40348192 | C | T | missense_variant | MODERATE | c.997C>T|p.Leu333Phe |
S237 |
6 | BAA03g66060 | A03 | 40348570 | G | A | missense_variant | MODERATE | c.1375G>A|p.Glu459Lys |
S234 |
7 | BAA03g66060 | A03 | 40348671 | C | T | synonymous_variant | LOW | c.1476C>T|p.Leu492Leu |
S153 |
8 | BAA03g66060 | A03 | 40348689 | G | C | missense_variant | MODERATE | c.1494G>C|p.Met498Ile |
S47 |
9 | BAA03g66060 | A03 | 40348953 | G | A | stop_gained | HIGH | c.1758G>A|p.Trp586* |
S270 |
10 | BAA03g66060 | A03 | 40349187 | G | A | synonymous_variant | LOW | c.1992G>A|p.Glu664Glu |
S296 |
11 | BAA03g66060 | A03 | 40349286 | C | T | synonymous_variant | LOW | c.2091C>T|p.Arg697Arg |
S205 |
12 | BAA03g66060 | A03 | 40349541 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2248-1G>A| |
S133 |
13 | BAA03g66060 | A03 | 40349819 | G | A | missense_variant | MODERATE | c.2525G>A|p.Arg842His |
S296 |
14 | BAA03g66060 | A03 | 40350700 | G | A | downstream_gene_variant | MODIFIER | c.*664G>A| |
S135 |
15 | BAA03g66060 | A03 | 40351033 | G | A | downstream_gene_variant | MODIFIER | c.*997G>A| |
S177 |
16 | BAA03g66060 | A03 | 40351778 | G | A | downstream_gene_variant | MODIFIER | c.*1742G>A| |
S255 |
17 | BAA03g66060 | A03 | 40352462 | G | A | downstream_gene_variant | MODIFIER | c.*2426G>A| |
S69 |
18 | BAA03g66060 | A03 | 40353023 | G | A | downstream_gene_variant | MODIFIER | c.*2987G>A| |
S202 |
19 | BAA03g66060 | A03 | 40353659 | C | T | downstream_gene_variant | MODIFIER | c.*3623C>T| |
S94 |
20 | BAA03g66060 | A03 | 40354790 | G | A | downstream_gene_variant | MODIFIER | c.*4754G>A| |
S146 |