Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44120 | A09 | 49934107 | G | A | missense_variant | MODERATE | c.446C>T|p.Ser149Leu |
S284 |
2 | BAA09g44120 | A09 | 49936067 | C | A | upstream_gene_variant | MODIFIER | c.-1515G>T| |
S116 S123 S140 S151 S154 S173 S174 S179 S202 S205 S216 S217 S255 S269 S278 S44 S49 S54 S59 |
3 | BAA09g44120 | A09 | 49936088 | C | T | upstream_gene_variant | MODIFIER | c.-1536G>A| |
S28 |
4 | BAA09g44120 | A09 | 49936123 | G | A | upstream_gene_variant | MODIFIER | c.-1571C>T| |
S143 |
5 | BAA09g44120 | A09 | 49937100 | T | A | upstream_gene_variant | MODIFIER | c.-2548A>T| |
S268 |
6 | BAA09g44120 | A09 | 49939309 | C | T | upstream_gene_variant | MODIFIER | c.-4757G>A| |
S238 |