Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01290 | A02 | 596139 | G | A | upstream_gene_variant | MODIFIER | c.-2122G>A| |
S283 |
2 | BAA02g01290 | A02 | 596881 | G | A | upstream_gene_variant | MODIFIER | c.-1380G>A| |
S265 |
3 | BAA02g01290 | A02 | 596883 | G | A | upstream_gene_variant | MODIFIER | c.-1378G>A| |
S162 |
4 | BAA02g01290 | A02 | 598252 | C | T | upstream_gene_variant | MODIFIER | c.-9C>T| |
S144 |
5 | BAA02g01290 | A02 | 598495 | C | T | missense_variant | MODERATE | c.124C>T|p.Leu42Phe |
S73 S91 |
6 | BAA02g01290 | A02 | 599372 | C | T | missense_variant | MODERATE | c.820C>T|p.Pro274Ser |
S19 |
7 | BAA02g01290 | A02 | 599617 | C | T | synonymous_variant | LOW | c.963C>T|p.Thr321Thr |
S116 |
8 | BAA02g01290 | A02 | 599712 | G | A | missense_variant | MODERATE | c.1058G>A|p.Gly353Glu |
S184 |
9 | BAA02g01290 | A02 | 599725 | T | C | synonymous_variant | LOW | c.1071T>C|p.Asp357Asp |
S17 |