Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38350 | A09 | 46256600 | C | T | missense_variant | MODERATE | c.464G>A|p.Gly155Asp |
S267 |
2 | BAA09g38350 | A09 | 46257325 | C | T | upstream_gene_variant | MODIFIER | c.-262G>A| |
S112 |
3 | BAA09g38350 | A09 | 46261695 | C | T | upstream_gene_variant | MODIFIER | c.-4632G>A| |
S114 |
4 | BAA09g38350 | A09 | 46261875 | G | A | upstream_gene_variant | MODIFIER | c.-4812C>T| |
S53 |
5 | BAA09g38350 | A09 | 46261896 | C | T | upstream_gene_variant | MODIFIER | c.-4833G>A| |
S56 |
6 | BAA09g38350 | A09 | 46262042 | C | T | upstream_gene_variant | MODIFIER | c.-4979G>A| |
S153 |