Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15130 | A01 | 7242143 | C | T | missense_variant | MODERATE | c.442G>A|p.Val148Ile |
S105 S106 |
2 | BAA01g15130 | A01 | 7244067 | C | T | upstream_gene_variant | MODIFIER | c.-1306G>A| |
S61 |
3 | BAA01g15130 | A01 | 7244396 | G | A | upstream_gene_variant | MODIFIER | c.-1635C>T| |
S194 |
4 | BAA01g15130 | A01 | 7244928 | C | T | upstream_gene_variant | MODIFIER | c.-2167G>A| |
S151 S263 |
5 | BAA01g15130 | A01 | 7245022 | C | T | upstream_gene_variant | MODIFIER | c.-2261G>A| |
S289 S290 |
6 | BAA01g15130 | A01 | 7245074 | G | A | upstream_gene_variant | MODIFIER | c.-2313C>T| |
S116 |
7 | BAA01g15130 | A01 | 7245241 | C | T | upstream_gene_variant | MODIFIER | c.-2480G>A| |
S33 |
8 | BAA01g15130 | A01 | 7245346 | G | A | upstream_gene_variant | MODIFIER | c.-2585C>T| |
S126 |
9 | BAA01g15130 | A01 | 7246263 | C | T | upstream_gene_variant | MODIFIER | c.-3502G>A| |
S223 |