| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g47160 | A01 | 31369765 | C | T | missense_variant | MODERATE | c.755G>A|p.Arg252Lys |
S79 S91 |
| 2 | BAA01g47160 | A01 | 31369898 | G | A | splice_region_variant&intron_variant | LOW | c.625-3C>T| |
S39 |
| 3 | BAA01g47160 | A01 | 31370266 | G | A | synonymous_variant | LOW | c.429C>T|p.Phe143Phe |
S120 |
| 4 | BAA01g47160 | A01 | 31372301 | G | A | upstream_gene_variant | MODIFIER | c.-911C>T| |
S72 S78 |
| 5 | BAA01g47160 | A01 | 31372574 | G | A | upstream_gene_variant | MODIFIER | c.-1184C>T| |
S200 |
| 6 | BAA01g47160 | A01 | 31373261 | C | T | upstream_gene_variant | MODIFIER | c.-1871G>A| |
S139 |
| 7 | BAA01g47160 | A01 | 31373481 | C | T | upstream_gene_variant | MODIFIER | c.-2091G>A| |
S194 |
| 8 | BAA01g47160 | A01 | 31376001 | G | A | upstream_gene_variant | MODIFIER | c.-4611C>T| |
S210 S225 |