Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02090 | A02 | 924734 | C | T | missense_variant | MODERATE | c.953G>A|p.Gly318Asp |
S8 |
2 | BAA02g02090 | A02 | 926227 | G | A | missense_variant | MODERATE | c.140C>T|p.Ser47Phe |
S280 |
3 | BAA02g02090 | A02 | 926265 | G | A | synonymous_variant | LOW | c.102C>T|p.Leu34Leu |
S162 |
4 | BAA02g02090 | A02 | 926270 | G | A | missense_variant | MODERATE | c.97C>T|p.Leu33Phe |
S296 |
5 | BAA02g02090 | A02 | 928504 | C | A | upstream_gene_variant | MODIFIER | c.-2138G>T| |
S68 |
6 | BAA02g02090 | A02 | 929635 | G | A | upstream_gene_variant | MODIFIER | c.-3269C>T| |
S237 |
7 | BAA02g02090 | A02 | 930380 | C | T | upstream_gene_variant | MODIFIER | c.-4014G>A| |
S111 |