Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00980 | A02 | 456963 | C | T | splice_region_variant&intron_variant | LOW | c.807-6G>A| |
S65 |
2 | BAA02g00980 | A02 | 457314 | G | A | synonymous_variant | LOW | c.525C>T|p.Leu175Leu |
S80 |
3 | BAA02g00980 | A02 | 458692 | C | T | upstream_gene_variant | MODIFIER | c.-188G>A| |
S144 |
4 | BAA02g00980 | A02 | 458777 | G | A | upstream_gene_variant | MODIFIER | c.-273C>T| |
S95 |
5 | BAA02g00980 | A02 | 459010 | C | T | upstream_gene_variant | MODIFIER | c.-506G>A| |
S306 S308 |
6 | BAA02g00980 | A02 | 460743 | C | T | upstream_gene_variant | MODIFIER | c.-2239G>A| |
S201 |
7 | BAA02g00980 | A02 | 461473 | G | A | upstream_gene_variant | MODIFIER | c.-2969C>T| |
S238 |
8 | BAA02g00980 | A02 | 463044 | G | A | upstream_gene_variant | MODIFIER | c.-4540C>T| |
S259 |