| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g08400 | A01 | 3696981 | G | A | missense_variant | MODERATE | c.2149C>T|p.Pro717Ser |
S280 |
| 2 | BAA01g08400 | A01 | 3697709 | G | A | synonymous_variant | LOW | c.1557C>T|p.Asp519Asp |
S271 |
| 3 | BAA01g08400 | A01 | 3698630 | C | T | missense_variant | MODERATE | c.989G>A|p.Gly330Glu |
S2 |
| 4 | BAA01g08400 | A01 | 3699526 | C | T | splice_donor_variant&intron_variant | HIGH | c.315+1G>A| |
S36 |
| 5 | BAA01g08400 | A01 | 3701427 | G | A | upstream_gene_variant | MODIFIER | c.-1491C>T| |
S262 |
| 6 | BAA01g08400 | A01 | 3701534 | C | T | upstream_gene_variant | MODIFIER | c.-1598G>A| |
S148 S210 S30 S31 |
| 7 | BAA01g08400 | A01 | 3701571 | G | A | upstream_gene_variant | MODIFIER | c.-1635C>T| |
S10 |
| 8 | BAA01g08400 | A01 | 3701986 | G | A | upstream_gene_variant | MODIFIER | c.-2050C>T| |
S297 |
| 9 | BAA01g08400 | A01 | 3703928 | C | T | upstream_gene_variant | MODIFIER | c.-3992G>A| |
S99 |
| 10 | BAA01g08400 | A01 | 3704209 | G | A | upstream_gene_variant | MODIFIER | c.-4273C>T| |
S209 |
| 11 | BAA01g08400 | A01 | 3704454 | G | A | upstream_gene_variant | MODIFIER | c.-4518C>T| |
S37 |
| 12 | BAA01g08400 | A01 | 3704849 | G | A | upstream_gene_variant | MODIFIER | c.-4913C>T| |
S183 S198 |