| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g45500 | A06 | 29019359 | C | T | upstream_gene_variant | MODIFIER | c.-4194C>T| |
S259 |
| 2 | BAA06g45500 | A06 | 29020988 | G | A | upstream_gene_variant | MODIFIER | c.-2565G>A| |
S274 S9 |
| 3 | BAA06g45500 | A06 | 29023168 | C | T | upstream_gene_variant | MODIFIER | c.-385C>T| |
S236 |
| 4 | BAA06g45500 | A06 | 29023352 | C | T | upstream_gene_variant | MODIFIER | c.-201C>T| |
S149 |
| 5 | BAA06g45500 | A06 | 29023745 | C | T | missense_variant | MODERATE | c.193C>T|p.Leu65Phe |
S69 |
| 6 | BAA06g45500 | A06 | 29023751 | C | T | missense_variant | MODERATE | c.199C>T|p.Pro67Ser |
S62 |
| 7 | BAA06g45500 | A06 | 29023752 | C | T | missense_variant | MODERATE | c.200C>T|p.Pro67Leu |
S262 |
| 8 | BAA06g45500 | A06 | 29023766 | G | A | missense_variant | MODERATE | c.214G>A|p.Ala72Thr |
S262 |
| 9 | BAA06g45500 | A06 | 29024148 | G | A | missense_variant | MODERATE | c.456G>A|p.Met152Ile |
S221 |
| 10 | BAA06g45500 | A06 | 29024366 | C | T | missense_variant | MODERATE | c.674C>T|p.Pro225Leu |
S217 |
| 11 | BAA06g45500 | A06 | 29024423 | C | T | missense_variant | MODERATE | c.731C>T|p.Ala244Val |
S262 |
| 12 | BAA06g45500 | A06 | 29024597 | C | T | missense_variant | MODERATE | c.905C>T|p.Ser302Phe |
S80 |
| 13 | BAA06g45500 | A06 | 29024631 | C | T | synonymous_variant | LOW | c.939C>T|p.Ser313Ser |
S105 S106 |
| 14 | BAA06g45500 | A06 | 29024765 | G | A | missense_variant | MODERATE | c.1073G>A|p.Gly358Asp |
S209 |
| 15 | BAA06g45500 | A06 | 29024897 | G | A | missense_variant | MODERATE | c.1205G>A|p.Arg402His |
S210 S225 |
| 16 | BAA06g45500 | A06 | 29024937 | C | T | synonymous_variant | LOW | c.1245C>T|p.Phe415Phe |
S94 |