| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g22660 | A08 | 16960346 | G | A | missense_variant | MODERATE | c.2525C>T|p.Ser842Phe |
S174 S39 |
| 2 | BAA08g22660 | A08 | 16960539 | C | T | missense_variant | MODERATE | c.2332G>A|p.Val778Ile |
S184 |
| 3 | BAA08g22660 | A08 | 16963259 | C | T | synonymous_variant | LOW | c.1746G>A|p.Leu582Leu |
S40 S49 |
| 4 | BAA08g22660 | A08 | 16964632 | C | T | missense_variant | MODERATE | c.1165G>A|p.Asp389Asn |
S156 |
| 5 | BAA08g22660 | A08 | 16965829 | G | A | missense_variant | MODERATE | c.521C>T|p.Ala174Val |
S203 |
| 6 | BAA08g22660 | A08 | 16966348 | C | T | missense_variant | MODERATE | c.203G>A|p.Gly68Glu |
S120 |
| 7 | BAA08g22660 | A08 | 16966504 | G | A | missense_variant | MODERATE | c.47C>T|p.Ser16Leu |
S41 |
| 8 | BAA08g22660 | A08 | 16966567 | G | A | upstream_gene_variant | MODIFIER | c.-17C>T| |
S125 |
| 9 | BAA08g22660 | A08 | 16968701 | G | A | upstream_gene_variant | MODIFIER | c.-2151C>T| |
S11 |
| 10 | BAA08g22660 | A08 | 16969794 | G | A | upstream_gene_variant | MODIFIER | c.-3244C>T| |
S282 |