Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44930 | A02 | 36900216 | C | T | downstream_gene_variant | MODIFIER | c.*4477G>A| |
S64 |
2 | BAA02g44930 | A02 | 36900539 | C | T | downstream_gene_variant | MODIFIER | c.*4154G>A| |
S1 S90 |
3 | BAA02g44930 | A02 | 36901361 | G | A | downstream_gene_variant | MODIFIER | c.*3332C>T| |
S264 |
4 | BAA02g44930 | A02 | 36901758 | G | A | downstream_gene_variant | MODIFIER | c.*2935C>T| |
S30 |
5 | BAA02g44930 | A02 | 36904787 | C | T | missense_variant | MODERATE | c.1949G>A|p.Cys650Tyr |
S189 |
6 | BAA02g44930 | A02 | 36904845 | G | A | missense_variant | MODERATE | c.1891C>T|p.Pro631Ser |
S207 |
7 | BAA02g44930 | A02 | 36905289 | G | A | missense_variant | MODERATE | c.1447C>T|p.Pro483Ser |
S67 |
8 | BAA02g44930 | A02 | 36905465 | C | T | missense_variant | MODERATE | c.1271G>A|p.Gly424Glu |
S168 |
9 | BAA02g44930 | A02 | 36905493 | G | A | missense_variant | MODERATE | c.1243C>T|p.Pro415Ser |
S36 |
10 | BAA02g44930 | A02 | 36906195 | G | A | missense_variant | MODERATE | c.541C>T|p.Pro181Ser |
S134 |
11 | BAA02g44930 | A02 | 36910986 | G | A | upstream_gene_variant | MODIFIER | c.-4251C>T| |
S28 |