| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g12980 | A09 | 7462669 | G | A | missense_variant | MODERATE | c.1274C>T|p.Thr425Ile |
S271 |
| 2 | BAA09g12980 | A09 | 7462729 | G | A | missense_variant | MODERATE | c.1214C>T|p.Ser405Phe |
S42 |
| 3 | BAA09g12980 | A09 | 7463376 | C | T | missense_variant | MODERATE | c.649G>A|p.Gly217Arg |
S206 S26 |
| 4 | BAA09g12980 | A09 | 7463395 | G | A | synonymous_variant | LOW | c.630C>T|p.Leu210Leu |
S198 |
| 5 | BAA09g12980 | A09 | 7463756 | C | T | synonymous_variant | LOW | c.426G>A|p.Lys142Lys |
S30 S31 |
| 6 | BAA09g12980 | A09 | 7463978 | C | T | splice_region_variant&intron_variant | LOW | c.302-4G>A| |
S82 S92 |
| 7 | BAA09g12980 | A09 | 7464475 | G | A | synonymous_variant | LOW | c.25C>T|p.Leu9Leu |
S115 |
| 8 | BAA09g12980 | A09 | 7466332 | C | T | upstream_gene_variant | MODIFIER | c.-1833G>A| |
S13 S219 S278 S279 S72 |
| 9 | BAA09g12980 | A09 | 7467921 | G | A | upstream_gene_variant | MODIFIER | c.-3422C>T| |
S210 S225 |