Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28190 | A02 | 15851535 | G | A | missense_variant | MODERATE | c.1160C>T|p.Ser387Phe |
S17 |
2 | BAA02g28190 | A02 | 15852632 | G | A | splice_region_variant&intron_variant | LOW | c.430-3C>T| |
S155 |
3 | BAA02g28190 | A02 | 15852828 | C | T | missense_variant | MODERATE | c.310G>A|p.Gly104Arg |
S53 |
4 | BAA02g28190 | A02 | 15856247 | G | A | upstream_gene_variant | MODIFIER | c.-2862C>T| |
S38 |
5 | BAA02g28190 | A02 | 15856581 | G | A | upstream_gene_variant | MODIFIER | c.-3196C>T| |
S281 |
6 | BAA02g28190 | A02 | 15856728 | C | T | upstream_gene_variant | MODIFIER | c.-3343G>A| |
S6 |
7 | BAA02g28190 | A02 | 15858019 | C | T | upstream_gene_variant | MODIFIER | c.-4634G>A| |
S182 |