| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g25280 | A01 | 13626090 | G | A | upstream_gene_variant | MODIFIER | c.-3739G>A| |
S59 |
| 2 | BAA01g25280 | A01 | 13630024 | C | T | missense_variant | MODERATE | c.125C>T|p.Ala42Val |
S182 |
| 3 | BAA01g25280 | A01 | 13632623 | G | A | missense_variant | MODERATE | c.1156G>A|p.Ala386Thr |
S71 |
| 4 | BAA01g25280 | A01 | 13632840 | G | A | intron_variant | MODIFIER | c.1324-42G>A| |
S275 |
| 5 | BAA01g25280 | A01 | 13634055 | G | A | missense_variant | MODERATE | c.2081G>A|p.Arg694Lys |
S299 |
| 6 | BAA01g25280 | A01 | 13634332 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2268-1G>A| |
S197 |
| 7 | BAA01g25280 | A01 | 13634534 | C | T | synonymous_variant | LOW | c.2469C>T|p.Phe823Phe |
S133 |
| 8 | BAA01g25280 | A01 | 13638869 | C | T | downstream_gene_variant | MODIFIER | c.*4140C>T| |
S206 |