| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g37960 | A05 | 37140265 | G | A | upstream_gene_variant | MODIFIER | c.-3107G>A| |
S132 S137 S89 |
| 2 | BAA05g37960 | A05 | 37147118 | C | T | missense_variant | MODERATE | c.2030C>T|p.Ala677Val |
S142 |
| 3 | BAA05g37960 | A05 | 37148468 | C | T | missense_variant | MODERATE | c.2920C>T|p.Leu974Phe |
S67 |
| 4 | BAA05g37960 | A05 | 37148548 | G | A | synonymous_variant | LOW | c.3000G>A|p.Glu1000Glu |
S150 |
| 5 | BAA05g37960 | A05 | 37149026 | G | A | missense_variant | MODERATE | c.3478G>A|p.Asp1160Asn |
S46 |
| 6 | BAA05g37960 | A05 | 37149143 | G | A | missense_variant | MODERATE | c.3595G>A|p.Glu1199Lys |
S164 |
| 7 | BAA05g37960 | A05 | 37150589 | G | A | synonymous_variant | LOW | c.4542G>A|p.Glu1514Glu |
S120 |
| 8 | BAA05g37960 | A05 | 37150615 | G | A | missense_variant | MODERATE | c.4568G>A|p.Arg1523His |
S271 |