| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g20440 | A02 | 10853977 | C | T | synonymous_variant | LOW | c.789G>A|p.Gly263Gly |
S75 S81 |
| 2 | BAA02g20440 | A02 | 10854712 | G | A | synonymous_variant | LOW | c.210C>T|p.Asp70Asp |
S92 |
| 3 | BAA02g20440 | A02 | 10854789 | C | T | missense_variant | MODERATE | c.133G>A|p.Asp45Asn |
S71 |
| 4 | BAA02g20440 | A02 | 10854833 | G | A | missense_variant | MODERATE | c.89C>T|p.Ser30Phe |
S157 |
| 5 | BAA02g20440 | A02 | 10855624 | G | A | upstream_gene_variant | MODIFIER | c.-703C>T| |
S146 |
| 6 | BAA02g20440 | A02 | 10856525 | C | T | upstream_gene_variant | MODIFIER | c.-1604G>A| |
S119 |
| 7 | BAA02g20440 | A02 | 10857969 | G | A | upstream_gene_variant | MODIFIER | c.-3048C>T| |
S33 |
| 8 | BAA02g20440 | A02 | 10858219 | C | T | upstream_gene_variant | MODIFIER | c.-3298G>A| |
S216 S241 S265 S39 |
| 9 | BAA02g20440 | A02 | 10859837 | G | A | upstream_gene_variant | MODIFIER | c.-4916C>T| |
S282 |