Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35660 | A02 | 30740052 | G | A | missense_variant | MODERATE | c.455C>T|p.Ser152Phe |
S86 |
2 | BAA02g35660 | A02 | 30740558 | G | A | missense_variant | MODERATE | c.31C>T|p.Pro11Ser |
S5 |
3 | BAA02g35660 | A02 | 30743695 | G | A | upstream_gene_variant | MODIFIER | c.-3107C>T| |
S197 |
4 | BAA02g35660 | A02 | 30743781 | G | A | upstream_gene_variant | MODIFIER | c.-3193C>T| |
S187 |
5 | BAA02g35660 | A02 | 30743851 | G | A | upstream_gene_variant | MODIFIER | c.-3263C>T| |
S11 |
6 | BAA02g35660 | A02 | 30744097 | G | A | upstream_gene_variant | MODIFIER | c.-3509C>T| |
S247 |
7 | BAA02g35660 | A02 | 30744199 | G | A | upstream_gene_variant | MODIFIER | c.-3611C>T| |
S225 S73 |
8 | BAA02g35660 | A02 | 30744656 | C | T | upstream_gene_variant | MODIFIER | c.-4068G>A| |
S139 |