| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g11960 | A10 | 13515798 | G | A | missense_variant | MODERATE | c.484C>T|p.Leu162Phe |
S125 |
| 2 | BAA10g11960 | A10 | 13516099 | C | T | synonymous_variant | LOW | c.183G>A|p.Glu61Glu |
S157 |
| 3 | BAA10g11960 | A10 | 13516622 | G | A | upstream_gene_variant | MODIFIER | c.-341C>T| |
S125 |
| 4 | BAA10g11960 | A10 | 13516728 | C | T | upstream_gene_variant | MODIFIER | c.-447G>A| |
S110 |
| 5 | BAA10g11960 | A10 | 13518096 | G | A | upstream_gene_variant | MODIFIER | c.-1815C>T| |
S293 |
| 6 | BAA10g11960 | A10 | 13519432 | C | T | upstream_gene_variant | MODIFIER | c.-3151G>A| |
S116 |
| 7 | BAA10g11960 | A10 | 13519674 | G | A | upstream_gene_variant | MODIFIER | c.-3393C>T| |
S174 S216 S241 S265 S39 |
| 8 | BAA10g11960 | A10 | 13520186 | G | A | upstream_gene_variant | MODIFIER | c.-3905C>T| |
S262 |
| 9 | BAA10g11960 | A10 | 13520190 | G | A | upstream_gene_variant | MODIFIER | c.-3909C>T| |
S45 |
| 10 | BAA10g11960 | A10 | 13520947 | C | T | upstream_gene_variant | MODIFIER | c.-4666G>A| |
S42 |