Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11640 | A02 | 5259127 | C | T | missense_variant | MODERATE | c.1715G>A|p.Gly572Glu |
S299 |
2 | BAA02g11640 | A02 | 5259921 | G | A | missense_variant | MODERATE | c.1187C>T|p.Thr396Ile |
S89 |
3 | BAA02g11640 | A02 | 5260183 | G | A | synonymous_variant | LOW | c.1005C>T|p.Leu335Leu |
S148 S210 S30 S31 |
4 | BAA02g11640 | A02 | 5264163 | C | T | upstream_gene_variant | MODIFIER | c.-1830G>A| |
S272 |
5 | BAA02g11640 | A02 | 5264556 | G | A | upstream_gene_variant | MODIFIER | c.-2223C>T| |
S189 |
6 | BAA02g11640 | A02 | 5265579 | G | A | upstream_gene_variant | MODIFIER | c.-3246C>T| |
S295 |
7 | BAA02g11640 | A02 | 5266561 | G | A | upstream_gene_variant | MODIFIER | c.-4228C>T| |
S146 |
8 | BAA02g11640 | A02 | 5267012 | C | T | upstream_gene_variant | MODIFIER | c.-4679G>A| |
S15 S3 |