Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g40130 | A05 | 38915151 | G | A | missense_variant | MODERATE | c.221C>T|p.Thr74Ile |
S301 S304 |
2 | BAA05g40130 | A05 | 38915887 | G | A | upstream_gene_variant | MODIFIER | c.-196C>T| |
S226 |
3 | BAA05g40130 | A05 | 38918851 | G | A | upstream_gene_variant | MODIFIER | c.-3160C>T| |
S75 S81 |
4 | BAA05g40130 | A05 | 38918974 | C | T | upstream_gene_variant | MODIFIER | c.-3283G>A| |
S192 |
5 | BAA05g40130 | A05 | 38919467 | C | T | upstream_gene_variant | MODIFIER | c.-3776G>A| |
S238 |
6 | BAA05g40130 | A05 | 38919569 | T | A | upstream_gene_variant | MODIFIER | c.-3878A>T| |
S26 |
7 | BAA05g40130 | A05 | 38919570 | C | T | upstream_gene_variant | MODIFIER | c.-3879G>A| |
S26 |
8 | BAA05g40130 | A05 | 38920584 | G | A | upstream_gene_variant | MODIFIER | c.-4893C>T| |
S107 |
9 | BAA05g40130 | A05 | 38920586 | G | A | upstream_gene_variant | MODIFIER | c.-4895C>T| |
S30 S31 |