Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07830 | A02 | 3369055 | C | T | missense_variant | MODERATE | c.1535G>A|p.Gly512Glu |
S174 S216 S265 S39 |
2 | BAA02g07830 | A02 | 3369625 | G | A | missense_variant | MODERATE | c.965C>T|p.Ser322Leu |
S206 S26 |
3 | BAA02g07830 | A02 | 3369677 | C | T | missense_variant | MODERATE | c.913G>A|p.Glu305Lys |
S185 |
4 | BAA02g07830 | A02 | 3369726 | C | T | synonymous_variant | LOW | c.864G>A|p.Lys288Lys |
S183 S198 |
5 | BAA02g07830 | A02 | 3370736 | G | A | upstream_gene_variant | MODIFIER | c.-147C>T| |
S164 |
6 | BAA02g07830 | A02 | 3370961 | C | T | upstream_gene_variant | MODIFIER | c.-372G>A| |
S39 |
7 | BAA02g07830 | A02 | 3374099 | G | A | upstream_gene_variant | MODIFIER | c.-3510C>T| |
S259 |
8 | BAA02g07830 | A02 | 3374779 | G | A | upstream_gene_variant | MODIFIER | c.-4190C>T| |
S173 |
9 | BAA02g07830 | A02 | 3375034 | C | T | upstream_gene_variant | MODIFIER | c.-4445G>A| |
S100 |