| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g08560 | A06 | 4393631 | C | T | missense_variant | MODERATE | c.2068G>A|p.Asp690Asn |
S282 |
| 2 | BAA06g08560 | A06 | 4394685 | C | T | missense_variant | MODERATE | c.1327G>A|p.Ala443Thr |
S134 |
| 3 | BAA06g08560 | A06 | 4394849 | G | A | missense_variant | MODERATE | c.1234C>T|p.Leu412Phe |
S69 |
| 4 | BAA06g08560 | A06 | 4395354 | G | A | synonymous_variant | LOW | c.729C>T|p.Ser243Ser |
S159 S299 |
| 5 | BAA06g08560 | A06 | 4395657 | C | T | synonymous_variant | LOW | c.426G>A|p.Lys142Lys |
S206 S26 |
| 6 | BAA06g08560 | A06 | 4397774 | C | T | upstream_gene_variant | MODIFIER | c.-1692G>A| |
S134 |
| 7 | BAA06g08560 | A06 | 4398899 | G | A | upstream_gene_variant | MODIFIER | c.-2817C>T| |
S176 |
| 8 | BAA06g08560 | A06 | 4399683 | C | T | upstream_gene_variant | MODIFIER | c.-3601G>A| |
S116 |