| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 23101 | BAA01g16690 | A01 | 8131562 | G | A | upstream_gene_variant | MODIFIER | c.-224G>A| |
S296 |
| 23102 | BAA01g16690 | A01 | 8132309 | C | T | missense_variant | MODERATE | c.347C>T|p.Ala116Val |
S206 |
| 23103 | BAA01g16690 | A01 | 8132873 | G | A | missense_variant | MODERATE | c.911G>A|p.Gly304Glu |
S37 |
| 23104 | BAA01g16690 | A01 | 8133011 | C | T | missense_variant | MODERATE | c.1049C>T|p.Ala350Val |
S19 |
| 23105 | BAA01g16690 | A01 | 8133587 | C | T | missense_variant | MODERATE | c.1625C>T|p.Ser542Phe |
S68 |
| 23106 | BAA01g16690 | A01 | 8133625 | G | A | missense_variant | MODERATE | c.1663G>A|p.Val555Ile |
S274 |
| 23107 | BAA01g16690 | A01 | 8133704 | G | A | stop_gained | HIGH | c.1742G>A|p.Trp581* |
S256 |
| 23108 | BAA01g16690 | A01 | 8133769 | G | A | missense_variant | MODERATE | c.1807G>A|p.Val603Met |
S301 S304 |
| 23109 | BAA01g16700 | A01 | 8134495 | C | T | missense_variant | MODERATE | c.146C>T|p.Pro49Leu |
S14 |
| 23110 | BAA01g16700 | A01 | 8134545 | G | A | missense_variant | MODERATE | c.196G>A|p.Gly66Arg |
S95 |
| 23111 | BAA01g16700 | A01 | 8134741 | G | A | missense_variant | MODERATE | c.392G>A|p.Gly131Glu |
S105 S106 |
| 23112 | BAA01g16700 | A01 | 8134821 | C | T | missense_variant | MODERATE | c.472C>T|p.Pro158Ser |
S206 S26 |
| 23113 | BAA01g16700 | A01 | 8134919 | G | A | synonymous_variant | LOW | c.570G>A|p.Pro190Pro |
S236 S83 S88 |
| 23114 | BAA01g16700 | A01 | 8134957 | C | T | missense_variant | MODERATE | c.608C>T|p.Pro203Leu |
S198 |
| 23115 | BAA01g16690 | A01 | 8135958 | G | A | downstream_gene_variant | MODIFIER | c.*1863G>A| |
S224 |
| 23116 | BAA01g16710 | A01 | 8136639 | G | A | synonymous_variant | LOW | c.772C>T|p.Leu258Leu |
S95 |
| 23117 | BAA01g16710 | A01 | 8137893 | G | A | synonymous_variant | LOW | c.163C>T|p.Leu55Leu |
S259 |
| 23118 | BAA01g16720 | A01 | 8139758 | C | T | missense_variant | MODERATE | c.644G>A|p.Gly215Glu |
S46 |
| 23119 | BAA01g16720 | A01 | 8139787 | G | A | synonymous_variant | LOW | c.615C>T|p.Asp205Asp |
S174 |
| 23120 | BAA01g16710 | A01 | 8139834 | G | A | upstream_gene_variant | MODIFIER | c.-1680C>T| |
S296 |
| 23121 | BAA01g16720 | A01 | 8139909 | G | A | splice_region_variant&intron_variant | LOW | c.579+7C>T| |
S175 |
| 23122 | BAA01g16710 | A01 | 8140598 | G | A | upstream_gene_variant | MODIFIER | c.-2444C>T| |
S262 |
| 23123 | BAA01g16720 | A01 | 8140635 | C | T | missense_variant&splice_region_variant | MODERATE | c.214G>A|p.Ala72Thr |
S36 |
| 23124 | BAA01g16720 | A01 | 8141071 | C | T | synonymous_variant | LOW | c.15G>A|p.Ser5Ser |
S62 |
| 23125 | BAA01g16720 | A01 | 8141082 | C | T | missense_variant | MODERATE | c.4G>A|p.Ala2Thr |
S260 |