| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g46750 | A09 | 51389491 | G | A | upstream_gene_variant | MODIFIER | c.-4849G>A| |
S16 |
| 2 | BAA09g46750 | A09 | 51390522 | G | A | upstream_gene_variant | MODIFIER | c.-3818G>A| |
S158 |
| 3 | BAA09g46750 | A09 | 51390933 | G | A | upstream_gene_variant | MODIFIER | c.-3407G>A| |
S10 |
| 4 | BAA09g46750 | A09 | 51393555 | G | A | upstream_gene_variant | MODIFIER | c.-785G>A| |
S290 |
| 5 | BAA09g46750 | A09 | 51394281 | C | T | upstream_gene_variant | MODIFIER | c.-59C>T| |
S260 |
| 6 | BAA09g46750 | A09 | 51395725 | C | T | missense_variant | MODERATE | c.862C>T|p.Leu288Phe |
S295 |
| 7 | BAA09g46750 | A09 | 51396330 | C | T | synonymous_variant | LOW | c.1248C>T|p.Phe416Phe |
S58 |
| 8 | BAA09g46750 | A09 | 51396556 | C | T | synonymous_variant | LOW | c.1321C>T|p.Leu441Leu |
S280 |
| 9 | BAA09g46750 | A09 | 51397515 | G | A | missense_variant | MODERATE | c.1855G>A|p.Asp619Asn |
S184 |
| 10 | BAA09g46750 | A09 | 51397971 | C | T | synonymous_variant | LOW | c.2149C>T|p.Leu717Leu |
S142 |