| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g05280 | A07 | 4659857 | C | T | upstream_gene_variant | MODIFIER | c.-4945C>T| |
S100 |
| 2 | BAA07g05280 | A07 | 4661173 | C | T | upstream_gene_variant | MODIFIER | c.-3629C>T| |
S116 |
| 3 | BAA07g05280 | A07 | 4663535 | G | A | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S264 |
| 4 | BAA07g05280 | A07 | 4663636 | C | T | upstream_gene_variant | MODIFIER | c.-1166C>T| |
S297 |
| 5 | BAA07g05280 | A07 | 4664667 | G | A | upstream_gene_variant | MODIFIER | c.-135G>A| |
S92 |
| 6 | BAA07g05280 | A07 | 4664811 | C | T | missense_variant | MODERATE | c.10C>T|p.Pro4Ser |
S242 |
| 7 | BAA07g05280 | A07 | 4666374 | G | A | synonymous_variant | LOW | c.837G>A|p.Glu279Glu |
S5 |
| 8 | BAA07g05280 | A07 | 4666501 | G | A | missense_variant | MODERATE | c.964G>A|p.Ala322Thr |
S142 |
| 9 | BAA07g05280 | A07 | 4666511 | G | A | missense_variant | MODERATE | c.974G>A|p.Gly325Glu |
S210 S225 |
| 10 | BAA07g05280 | A07 | 4666595 | G | A | missense_variant | MODERATE | c.1058G>A|p.Gly353Glu |
S183 |
| 11 | BAA07g05280 | A07 | 4666913 | G | A | synonymous_variant | LOW | c.1284G>A|p.Lys428Lys |
S65 |
| 12 | BAA07g05280 | A07 | 4667008 | C | T | missense_variant | MODERATE | c.1379C>T|p.Pro460Leu |
S138 |
| 13 | BAA07g05280 | A07 | 4669533 | C | T | downstream_gene_variant | MODIFIER | c.*2329C>T| |
S121 |
| 14 | BAA07g05280 | A07 | 4669977 | C | T | downstream_gene_variant | MODIFIER | c.*2773C>T| |
S279 |
| 15 | BAA07g05280 | A07 | 4671339 | G | A | downstream_gene_variant | MODIFIER | c.*4135G>A| |
S62 |
| 16 | BAA07g05280 | A07 | 4671757 | C | T | downstream_gene_variant | MODIFIER | c.*4553C>T| |
S289 S290 |
| 17 | BAA07g05280 | A07 | 4671920 | C | T | downstream_gene_variant | MODIFIER | c.*4716C>T| |
S133 |