| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g18980 | A08 | 15048878 | G | A | synonymous_variant | LOW | c.1245C>T|p.Arg415Arg |
S122 |
| 2 | BAA08g18980 | A08 | 15049127 | G | A | missense_variant | MODERATE | c.1082C>T|p.Pro361Leu |
S282 |
| 3 | BAA08g18980 | A08 | 15049133 | G | A | missense_variant | MODERATE | c.1076C>T|p.Pro359Leu |
S99 |
| 4 | BAA08g18980 | A08 | 15050128 | C | T | missense_variant | MODERATE | c.601G>A|p.Glu201Lys |
S197 |
| 5 | BAA08g18980 | A08 | 15050753 | G | A | missense_variant | MODERATE | c.452C>T|p.Pro151Leu |
S66 |
| 6 | BAA08g18980 | A08 | 15051821 | G | A | upstream_gene_variant | MODIFIER | c.-617C>T| |
S292 |
| 7 | BAA08g18980 | A08 | 15052067 | C | T | upstream_gene_variant | MODIFIER | c.-863G>A| |
S293 |
| 8 | BAA08g18980 | A08 | 15052418 | C | T | upstream_gene_variant | MODIFIER | c.-1214G>A| |
S276 |
| 9 | BAA08g18980 | A08 | 15052542 | C | T | upstream_gene_variant | MODIFIER | c.-1338G>A| |
S156 |
| 10 | BAA08g18980 | A08 | 15052560 | G | A | upstream_gene_variant | MODIFIER | c.-1356C>T| |
S116 |
| 11 | BAA08g18980 | A08 | 15052799 | C | T | upstream_gene_variant | MODIFIER | c.-1595G>A| |
S183 S198 |
| 12 | BAA08g18980 | A08 | 15052977 | G | A | upstream_gene_variant | MODIFIER | c.-1773C>T| |
S122 |
| 13 | BAA08g18980 | A08 | 15053502 | G | A | upstream_gene_variant | MODIFIER | c.-2298C>T| |
S153 |
| 14 | BAA08g18980 | A08 | 15054003 | G | A | upstream_gene_variant | MODIFIER | c.-2799C>T| |
S37 |