Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09630 | A02 | 4231790 | G | A | missense_variant | MODERATE | c.530C>T|p.Pro177Leu |
S143 |
2 | BAA02g09630 | A02 | 4232049 | C | T | missense_variant | MODERATE | c.271G>A|p.Val91Ile |
S233 |
3 | BAA02g09630 | A02 | 4232084 | G | A | missense_variant | MODERATE | c.236C>T|p.Ala79Val |
S7 |
4 | BAA02g09630 | A02 | 4233955 | C | T | upstream_gene_variant | MODIFIER | c.-1636G>A| |
S230 |
5 | BAA02g09630 | A02 | 4234023 | C | T | upstream_gene_variant | MODIFIER | c.-1704G>A| |
S157 |
6 | BAA02g09630 | A02 | 4234970 | G | A | upstream_gene_variant | MODIFIER | c.-2651C>T| |
S207 |
7 | BAA02g09630 | A02 | 4235942 | G | A | upstream_gene_variant | MODIFIER | c.-3623C>T| |
S282 |