| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g46990 | A09 | 51495982 | C | T | missense_variant | MODERATE | c.850G>A|p.Asp284Asn |
S121 |
| 2 | BAA09g46990 | A09 | 51497327 | G | A | missense_variant | MODERATE | c.251C>T|p.Ser84Phe |
S216 |
| 3 | BAA09g46990 | A09 | 51497342 | G | A | missense_variant | MODERATE | c.236C>T|p.Ser79Phe |
S233 |
| 4 | BAA09g46990 | A09 | 51497474 | G | A | missense_variant | MODERATE | c.104C>T|p.Ser35Phe |
S116 |
| 5 | BAA09g46990 | A09 | 51499243 | G | A | upstream_gene_variant | MODIFIER | c.-1666C>T| |
S150 |
| 6 | BAA09g46990 | A09 | 51499821 | C | T | upstream_gene_variant | MODIFIER | c.-2244G>A| |
S277 |
| 7 | BAA09g46990 | A09 | 51502566 | G | A | upstream_gene_variant | MODIFIER | c.-4989C>T| |
S132 |