Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00240 | A07 | 113103 | C | T | missense_variant | MODERATE | c.208G>A|p.Ala70Thr |
S18 |
2 | BAA07g00240 | A07 | 113225 | G | A | synonymous_variant | LOW | c.186C>T|p.Phe62Phe |
S208 S219 |
3 | BAA07g00240 | A07 | 113432 | C | T | upstream_gene_variant | MODIFIER | c.-22G>A| |
S32 |
4 | BAA07g00240 | A07 | 113564 | G | A | upstream_gene_variant | MODIFIER | c.-154C>T| |
S245 |
5 | BAA07g00240 | A07 | 113598 | C | T | upstream_gene_variant | MODIFIER | c.-188G>A| |
S155 S211 |
6 | BAA07g00240 | A07 | 116247 | G | A | upstream_gene_variant | MODIFIER | c.-2837C>T| |
S30 S31 |
7 | BAA07g00240 | A07 | 116848 | C | T | upstream_gene_variant | MODIFIER | c.-3438G>A| |
S142 |
8 | BAA07g00240 | A07 | 116910 | C | T | upstream_gene_variant | MODIFIER | c.-3500G>A| |
S247 |
9 | BAA07g00240 | A07 | 117102 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S167 |
10 | BAA07g00240 | A07 | 117676 | C | T | upstream_gene_variant | MODIFIER | c.-4266G>A| |
S305 |