Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18710 | A02 | 9614136 | T | A | intron_variant | MODIFIER | c.691+9A>T| |
S283 |
2 | BAA02g18710 | A02 | 9614207 | G | A | missense_variant | MODERATE | c.629C>T|p.Pro210Leu |
S298 |
3 | BAA02g18710 | A02 | 9618202 | C | T | upstream_gene_variant | MODIFIER | c.-596G>A| |
S255 S283 |
4 | BAA02g18710 | A02 | 9618593 | G | A | upstream_gene_variant | MODIFIER | c.-987C>T| |
S240 |
5 | BAA02g18710 | A02 | 9618655 | G | A | upstream_gene_variant | MODIFIER | c.-1049C>T| |
S169 |
6 | BAA02g18710 | A02 | 9619355 | G | A | upstream_gene_variant | MODIFIER | c.-1749C>T| |
S169 |
7 | BAA02g18710 | A02 | 9619428 | C | T | upstream_gene_variant | MODIFIER | c.-1822G>A| |
S266 |
8 | BAA02g18710 | A02 | 9621271 | G | A | upstream_gene_variant | MODIFIER | c.-3665C>T| |
S162 |
9 | BAA02g18710 | A02 | 9622262 | C | T | upstream_gene_variant | MODIFIER | c.-4656G>A| |
S58 |