Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38190 | A09 | 46175151 | G | A | missense_variant | MODERATE | c.785C>T|p.Ala262Val |
S298 |
2 | BAA09g38190 | A09 | 46177803 | G | A | synonymous_variant | LOW | c.84C>T|p.Leu28Leu |
S226 |
3 | BAA09g38190 | A09 | 46178166 | G | A | upstream_gene_variant | MODIFIER | c.-280C>T| |
S160 |
4 | BAA09g38190 | A09 | 46178909 | G | T | upstream_gene_variant | MODIFIER | c.-1023C>A| |
S133 |
5 | BAA09g38190 | A09 | 46179139 | G | A | upstream_gene_variant | MODIFIER | c.-1253C>T| |
S35 |
6 | BAA09g38190 | A09 | 46181264 | G | A | upstream_gene_variant | MODIFIER | c.-3378C>T| |
S167 |
7 | BAA09g38190 | A09 | 46182011 | C | T | upstream_gene_variant | MODIFIER | c.-4125G>A| |
S187 |
8 | BAA09g38190 | A09 | 46182063 | C | T | upstream_gene_variant | MODIFIER | c.-4177G>A| |
S124 |
9 | BAA09g38190 | A09 | 46182389 | C | T | upstream_gene_variant | MODIFIER | c.-4503G>A| |
S186 |