| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g22740 | A03 | 10365001 | C | T | downstream_gene_variant | MODIFIER | c.*1639G>A| |
S265 |
| 2 | BAA03g22740 | A03 | 10366583 | C | T | downstream_gene_variant | MODIFIER | c.*57G>A| |
S8 |
| 3 | BAA03g22740 | A03 | 10366604 | G | A | downstream_gene_variant | MODIFIER | c.*36C>T| |
S17 |
| 4 | BAA03g22740 | A03 | 10366658 | C | T | synonymous_variant | LOW | c.1323G>A|p.Arg441Arg |
S11 |
| 5 | BAA03g22740 | A03 | 10366716 | C | T | missense_variant | MODERATE | c.1265G>A|p.Gly422Glu |
S61 |
| 6 | BAA03g22740 | A03 | 10366843 | C | T | missense_variant | MODERATE | c.1138G>A|p.Glu380Lys |
S176 |
| 7 | BAA03g22740 | A03 | 10366938 | C | T | missense_variant | MODERATE | c.1043G>A|p.Gly348Glu |
S305 |
| 8 | BAA03g22740 | A03 | 10367192 | G | A | splice_region_variant&intron_variant | LOW | c.929-4C>T| |
S88 |
| 9 | BAA03g22740 | A03 | 10367261 | C | T | intron_variant | MODIFIER | c.929-73G>A| |
S113 S117 S120 S266 S297 S9 |
| 10 | BAA03g22740 | A03 | 10371701 | G | A | synonymous_variant | LOW | c.258C>T|p.Ile86Ile |
S70 |
| 11 | BAA03g22740 | A03 | 10374635 | G | A | upstream_gene_variant | MODIFIER | c.-2677C>T| |
S4 |