Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43930 | A02 | 36278105 | G | A | missense_variant | MODERATE | c.1249C>T|p.Pro417Ser |
S184 |
2 | BAA02g43930 | A02 | 36278405 | C | T | missense_variant | MODERATE | c.1091G>A|p.Gly364Glu |
S63 |
3 | BAA02g43930 | A02 | 36278510 | C | T | missense_variant&splice_region_variant | MODERATE | c.1061G>A|p.Gly354Glu |
S159 S243 |
4 | BAA02g43930 | A02 | 36279792 | G | A | missense_variant | MODERATE | c.385C>T|p.Arg129Trp |
S5 |
5 | BAA02g43930 | A02 | 36282186 | G | A | upstream_gene_variant | MODIFIER | c.-1365C>T| |
S155 S211 |
6 | BAA02g43930 | A02 | 36284595 | G | A | upstream_gene_variant | MODIFIER | c.-3774C>T| |
S43 |
7 | BAA02g43930 | A02 | 36285014 | C | T | upstream_gene_variant | MODIFIER | c.-4193G>A| |
S299 |
8 | BAA02g43930 | A02 | 36285144 | G | A | upstream_gene_variant | MODIFIER | c.-4323C>T| |
S66 |