| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g24740 | A08 | 18020136 | G | A | missense_variant | MODERATE | c.1489C>T|p.Arg497Cys |
S289 S290 |
| 2 | BAA08g24740 | A08 | 18020466 | C | T | missense_variant | MODERATE | c.1159G>A|p.Val387Ile |
S11 |
| 3 | BAA08g24740 | A08 | 18021539 | A | G | synonymous_variant | LOW | c.516T>C|p.Ile172Ile |
S34 |
| 4 | BAA08g24740 | A08 | 18021838 | G | A | missense_variant | MODERATE | c.301C>T|p.Leu101Phe |
S188 |
| 5 | BAA08g24740 | A08 | 18022155 | G | A | synonymous_variant | LOW | c.192C>T|p.Val64Val |
S136 |
| 6 | BAA08g24740 | A08 | 18022353 | G | A | upstream_gene_variant | MODIFIER | c.-7C>T| |
S155 S211 |
| 7 | BAA08g24740 | A08 | 18023120 | G | A | upstream_gene_variant | MODIFIER | c.-774C>T| |
S275 |
| 8 | BAA08g24740 | A08 | 18023545 | G | A | upstream_gene_variant | MODIFIER | c.-1199C>T| |
S120 S266 S65 |
| 9 | BAA08g24740 | A08 | 18024439 | C | T | upstream_gene_variant | MODIFIER | c.-2093G>A| |
S224 |
| 10 | BAA08g24740 | A08 | 18024697 | C | T | upstream_gene_variant | MODIFIER | c.-2351G>A| |
S201 |
| 11 | BAA08g24740 | A08 | 18024788 | G | A | upstream_gene_variant | MODIFIER | c.-2442C>T| |
S116 |
| 12 | BAA08g24740 | A08 | 18024858 | C | T | upstream_gene_variant | MODIFIER | c.-2512G>A| |
S110 |
| 13 | BAA08g24740 | A08 | 18025462 | C | T | upstream_gene_variant | MODIFIER | c.-3116G>A| |
S6 |
| 14 | BAA08g24740 | A08 | 18025880 | C | T | upstream_gene_variant | MODIFIER | c.-3534G>A| |
S156 |