Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15600 | A02 | 7534550 | G | A | upstream_gene_variant | MODIFIER | c.-3950G>A| |
S51 |
2 | BAA02g15600 | A02 | 7535629 | G | C | upstream_gene_variant | MODIFIER | c.-2871G>C| |
S125 |
3 | BAA02g15600 | A02 | 7535765 | G | A | upstream_gene_variant | MODIFIER | c.-2735G>A| |
S207 |
4 | BAA02g15600 | A02 | 7537906 | C | T | upstream_gene_variant | MODIFIER | c.-594C>T| |
S23 |
5 | BAA02g15600 | A02 | 7538161 | C | T | upstream_gene_variant | MODIFIER | c.-339C>T| |
S181 |
6 | BAA02g15600 | A02 | 7538362 | C | T | upstream_gene_variant | MODIFIER | c.-138C>T| |
S186 |
7 | BAA02g15600 | A02 | 7539175 | G | A | missense_variant | MODERATE | c.676G>A|p.Glu226Lys |
S264 |
8 | BAA02g15600 | A02 | 7539405 | C | T | synonymous_variant | LOW | c.906C>T|p.Val302Val |
S63 |
9 | BAA02g15600 | A02 | 7539427 | G | A | missense_variant | MODERATE | c.928G>A|p.Asp310Asn |
S187 |
10 | BAA02g15600 | A02 | 7539680 | C | T | missense_variant | MODERATE | c.1028C>T|p.Thr343Met |
S25 |
11 | BAA02g15600 | A02 | 7540818 | C | T | downstream_gene_variant | MODIFIER | c.*95C>T| |
S182 |
12 | BAA02g15600 | A02 | 7541509 | C | T | downstream_gene_variant | MODIFIER | c.*786C>T| |
S216 S241 S265 S39 |
13 | BAA02g15600 | A02 | 7542235 | G | A | downstream_gene_variant | MODIFIER | c.*1512G>A| |
S37 |
14 | BAA02g15600 | A02 | 7542375 | G | A | downstream_gene_variant | MODIFIER | c.*1652G>A| |
S62 |