Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22500 | A02 | 12162712 | C | T | upstream_gene_variant | MODIFIER | c.-4184C>T| |
S144 |
2 | BAA02g22500 | A02 | 12162901 | G | A | upstream_gene_variant | MODIFIER | c.-3995G>A| |
S74 |
3 | BAA02g22500 | A02 | 12162958 | G | A | upstream_gene_variant | MODIFIER | c.-3938G>A| |
S303 |
4 | BAA02g22500 | A02 | 12163234 | C | T | upstream_gene_variant | MODIFIER | c.-3662C>T| |
S289 S290 |
5 | BAA02g22500 | A02 | 12167140 | G | A | missense_variant | MODERATE | c.167G>A|p.Gly56Glu |
S237 |
6 | BAA02g22500 | A02 | 12167240 | G | A | synonymous_variant | LOW | c.267G>A|p.Ser89Ser |
S263 |
7 | BAA02g22500 | A02 | 12167673 | G | A | missense_variant | MODERATE | c.463G>A|p.Ala155Thr |
S74 |
8 | BAA02g22500 | A02 | 12169043 | G | A | downstream_gene_variant | MODIFIER | c.*102G>A| |
S263 |
9 | BAA02g22500 | A02 | 12170117 | C | T | downstream_gene_variant | MODIFIER | c.*1176C>T| |
S233 |
10 | BAA02g22500 | A02 | 12170765 | G | A | downstream_gene_variant | MODIFIER | c.*1824G>A| |
S298 |
11 | BAA02g22500 | A02 | 12170844 | G | A | downstream_gene_variant | MODIFIER | c.*1903G>A| |
S188 |
12 | BAA02g22500 | A02 | 12172241 | G | A | downstream_gene_variant | MODIFIER | c.*3300G>A| |
S190 |
13 | BAA02g22500 | A02 | 12173674 | C | T | downstream_gene_variant | MODIFIER | c.*4733C>T| |
S87 |