| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g28840 | A08 | 19954839 | C | T | upstream_gene_variant | MODIFIER | c.-3323C>T| |
S299 |
| 2 | BAA08g28840 | A08 | 19955549 | C | T | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S32 |
| 3 | BAA08g28840 | A08 | 19956858 | G | A | upstream_gene_variant | MODIFIER | c.-1304G>A| |
S62 |
| 4 | BAA08g28840 | A08 | 19958553 | C | T | missense_variant | MODERATE | c.121C>T|p.Leu41Phe |
S57 |
| 5 | BAA08g28840 | A08 | 19961643 | C | T | missense_variant | MODERATE | c.2458C>T|p.Leu820Phe |
S262 |
| 6 | BAA08g28840 | A08 | 19961860 | G | A | missense_variant | MODERATE | c.2675G>A|p.Arg892Gln |
S122 |
| 7 | BAA08g28840 | A08 | 19962042 | C | T | missense_variant | MODERATE | c.2857C>T|p.Leu953Phe |
S19 |
| 8 | BAA08g28840 | A08 | 19962237 | C | T | missense_variant | MODERATE | c.2972C>T|p.Ala991Val |
S262 |
| 9 | BAA08g28840 | A08 | 19962284 | G | A | missense_variant | MODERATE | c.3019G>A|p.Val1007Ile |
S218 |
| 10 | BAA08g28840 | A08 | 19963833 | G | A | downstream_gene_variant | MODIFIER | c.*1505G>A| |
S42 |
| 11 | BAA08g28840 | A08 | 19964303 | G | A | downstream_gene_variant | MODIFIER | c.*1975G>A| |
S287 |
| 12 | BAA08g28840 | A08 | 19965620 | G | A | downstream_gene_variant | MODIFIER | c.*3292G>A| |
S42 |