Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46970 | A02 | 38025486 | C | T | downstream_gene_variant | MODIFIER | c.*4165G>A| |
S173 |
2 | BAA02g46970 | A02 | 38025551 | G | A | downstream_gene_variant | MODIFIER | c.*4100C>T| |
S139 |
3 | BAA02g46970 | A02 | 38029859 | C | T | missense_variant | MODERATE | c.1538G>A|p.Gly513Glu |
S13 |
4 | BAA02g46970 | A02 | 38030301 | C | T | missense_variant | MODERATE | c.1096G>A|p.Val366Met |
S76 |
5 | BAA02g46970 | A02 | 38030482 | C | T | synonymous_variant | LOW | c.915G>A|p.Lys305Lys |
S273 |
6 | BAA02g46970 | A02 | 38030606 | C | T | stop_gained | HIGH | c.791G>A|p.Trp264* |
S133 |
7 | BAA02g46970 | A02 | 38031374 | G | A | missense_variant | MODERATE | c.23C>T|p.Pro8Leu |
S157 S163 |
8 | BAA02g46970 | A02 | 38032322 | G | A | upstream_gene_variant | MODIFIER | c.-926C>T| |
S132 S137 S215 S89 |
9 | BAA02g46970 | A02 | 38033468 | C | T | upstream_gene_variant | MODIFIER | c.-2072G>A| |
S201 |