Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44610 | A09 | 50192997 | G | A | missense_variant | MODERATE | c.508C>T|p.Arg170Cys |
S167 |
2 | BAA09g44610 | A09 | 50193134 | T | A | synonymous_variant | LOW | c.441A>T|p.Leu147Leu |
S39 |
3 | BAA09g44610 | A09 | 50193980 | G | A | synonymous_variant | LOW | c.81C>T|p.Leu27Leu |
S262 |
4 | BAA09g44610 | A09 | 50194046 | G | A | synonymous_variant | LOW | c.15C>T|p.Leu5Leu |
S98 |
5 | BAA09g44610 | A09 | 50197741 | C | T | upstream_gene_variant | MODIFIER | c.-3681G>A| |
S56 |
6 | BAA09g44610 | A09 | 50198156 | G | A | upstream_gene_variant | MODIFIER | c.-4096C>T| |
S98 |
7 | BAA09g44610 | A09 | 50198455 | C | T | upstream_gene_variant | MODIFIER | c.-4395G>A| |
S259 |
8 | BAA09g44610 | A09 | 50198634 | G | A | upstream_gene_variant | MODIFIER | c.-4574C>T| |
S202 |
9 | BAA09g44610 | A09 | 50198637 | G | A | upstream_gene_variant | MODIFIER | c.-4577C>T| |
S246 |