| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g13180 | A09 | 7570417 | C | A | upstream_gene_variant | MODIFIER | c.-1775C>A| |
S96 |
| 2 | BAA09g13180 | A09 | 7572555 | C | T | missense_variant | MODERATE | c.266C>T|p.Thr89Ile |
S263 |
| 3 | BAA09g13180 | A09 | 7572916 | G | A | splice_region_variant&intron_variant | LOW | c.531+5G>A| |
S172 |
| 4 | BAA09g13180 | A09 | 7573530 | G | A | missense_variant | MODERATE | c.925G>A|p.Glu309Lys |
S8 |
| 5 | BAA09g13180 | A09 | 7574263 | C | T | missense_variant | MODERATE | c.1496C>T|p.Ser499Phe |
S82 S92 |
| 6 | BAA09g13180 | A09 | 7574265 | C | T | missense_variant | MODERATE | c.1498C>T|p.Leu500Phe |
S132 S137 S215 |
| 7 | BAA09g13180 | A09 | 7576933 | G | A | downstream_gene_variant | MODIFIER | c.*2591G>A| |
S228 |
| 8 | BAA09g13180 | A09 | 7577006 | T | G | downstream_gene_variant | MODIFIER | c.*2664T>G| |
S146 S148 S157 S167 S193 S211 S222 S239 S244 S283 S89 |
| 9 | BAA09g13180 | A09 | 7577239 | G | A | downstream_gene_variant | MODIFIER | c.*2897G>A| |
S288 |