Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00930 | A02 | 434083 | C | T | upstream_gene_variant | MODIFIER | c.-4472C>T| |
S278 |
2 | BAA02g00930 | A02 | 436086 | G | T | upstream_gene_variant | MODIFIER | c.-2469G>T| |
S134 S179 |
3 | BAA02g00930 | A02 | 436176 | C | T | upstream_gene_variant | MODIFIER | c.-2379C>T| |
S278 |
4 | BAA02g00930 | A02 | 436700 | G | A | upstream_gene_variant | MODIFIER | c.-1855G>A| |
S64 |
5 | BAA02g00930 | A02 | 436841 | G | A | upstream_gene_variant | MODIFIER | c.-1714G>A| |
S43 |
6 | BAA02g00930 | A02 | 437898 | C | T | upstream_gene_variant | MODIFIER | c.-657C>T| |
S159 |
7 | BAA02g00930 | A02 | 438447 | G | A | upstream_gene_variant | MODIFIER | c.-108G>A| |
S259 |
8 | BAA02g00930 | A02 | 439138 | G | A | synonymous_variant | LOW | c.492G>A|p.Gly164Gly |
S23 |
9 | BAA02g00930 | A02 | 439537 | C | T | splice_region_variant&synonymous_variant | LOW | c.654C>T|p.Phe218Phe |
S55 |
10 | BAA02g00930 | A02 | 440095 | G | A | missense_variant&splice_region_variant | MODERATE | c.932G>A|p.Gly311Glu |
S173 |