Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04750 | A02 | 2061522 | C | T | missense_variant | MODERATE | c.956G>A|p.Gly319Glu |
S272 |
2 | BAA02g04750 | A02 | 2061907 | C | T | intron_variant | MODIFIER | c.829+122G>A| |
S138 |
3 | BAA02g04750 | A02 | 2062329 | C | T | missense_variant | MODERATE | c.529G>A|p.Ala177Thr |
S301 S304 |
4 | BAA02g04750 | A02 | 2063075 | C | T | upstream_gene_variant | MODIFIER | c.-218G>A| |
S240 |
5 | BAA02g04750 | A02 | 2063096 | G | A | upstream_gene_variant | MODIFIER | c.-239C>T| |
S259 |
6 | BAA02g04750 | A02 | 2063100 | C | T | upstream_gene_variant | MODIFIER | c.-243G>A| |
S152 |
7 | BAA02g04750 | A02 | 2063283 | C | T | upstream_gene_variant | MODIFIER | c.-426G>A| |
S212 |
8 | BAA02g04750 | A02 | 2064058 | G | A | upstream_gene_variant | MODIFIER | c.-1201C>T| |
S52 |
9 | BAA02g04750 | A02 | 2065616 | G | A | upstream_gene_variant | MODIFIER | c.-2759C>T| |
S28 |
10 | BAA02g04750 | A02 | 2066348 | C | T | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S226 |
11 | BAA02g04750 | A02 | 2066387 | C | T | upstream_gene_variant | MODIFIER | c.-3530G>A| |
S202 |