| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g19390 | A05 | 11427487 | G | A | missense_variant | MODERATE | c.635C>T|p.Ser212Phe |
S152 |
| 2 | BAA05g19390 | A05 | 11427650 | G | A | missense_variant | MODERATE | c.472C>T|p.Pro158Ser |
S40 S49 |
| 3 | BAA05g19390 | A05 | 11427998 | C | T | missense_variant | MODERATE | c.188G>A|p.Arg63Lys |
S36 |
| 4 | BAA05g19390 | A05 | 11428113 | C | T | missense_variant | MODERATE | c.73G>A|p.Asp25Asn |
S30 S31 |
| 5 | BAA05g19390 | A05 | 11428163 | C | T | missense_variant | MODERATE | c.23G>A|p.Gly8Glu |
S153 S213 |
| 6 | BAA05g19390 | A05 | 11428337 | C | T | upstream_gene_variant | MODIFIER | c.-152G>A| |
S188 |
| 7 | BAA05g19390 | A05 | 11428351 | C | T | upstream_gene_variant | MODIFIER | c.-166G>A| |
S13 |
| 8 | BAA05g19390 | A05 | 11431867 | G | A | upstream_gene_variant | MODIFIER | c.-3682C>T| |
S150 |
| 9 | BAA05g19390 | A05 | 11433158 | T | A | upstream_gene_variant | MODIFIER | c.-4973A>T| |
S118 |