Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g23120 | A02 | 12597314 | C | T | missense_variant | MODERATE | c.916G>A|p.Glu306Lys |
S289 S290 |
2 | BAA02g23120 | A02 | 12597408 | C | T | intron_variant | MODIFIER | c.873+31G>A| |
S152 |
3 | BAA02g23120 | A02 | 12597620 | C | T | intron_variant | MODIFIER | c.721-29G>A| |
S283 |
4 | BAA02g23120 | A02 | 12599799 | G | A | upstream_gene_variant | MODIFIER | c.-889C>T| |
S37 |
5 | BAA02g23120 | A02 | 12600350 | G | A | upstream_gene_variant | MODIFIER | c.-1440C>T| |
S13 S261 |
6 | BAA02g23120 | A02 | 12601038 | C | T | upstream_gene_variant | MODIFIER | c.-2128G>A| |
S123 |
7 | BAA02g23120 | A02 | 12601591 | G | A | upstream_gene_variant | MODIFIER | c.-2681C>T| |
S111 |
8 | BAA02g23120 | A02 | 12602298 | G | A | upstream_gene_variant | MODIFIER | c.-3388C>T| |
S5 |