Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12700 | A08 | 11101016 | G | A | upstream_gene_variant | MODIFIER | c.-241G>A| |
S122 |
2 | BAA08g12700 | A08 | 11101062 | C | T | upstream_gene_variant | MODIFIER | c.-195C>T| |
S60 |
3 | BAA08g12700 | A08 | 11101383 | C | T | intron_variant | MODIFIER | c.31-51C>T| |
S256 |
4 | BAA08g12700 | A08 | 11101692 | C | T | missense_variant | MODERATE | c.193C>T|p.Leu65Phe |
S156 |
5 | BAA08g12700 | A08 | 11101896 | G | A | downstream_gene_variant | MODIFIER | c.*175G>A| |
S133 |
6 | BAA08g12700 | A08 | 11102233 | G | A | downstream_gene_variant | MODIFIER | c.*512G>A| |
S115 |
7 | BAA08g12700 | A08 | 11102385 | G | A | downstream_gene_variant | MODIFIER | c.*664G>A| |
S262 |
8 | BAA08g12700 | A08 | 11102694 | C | T | downstream_gene_variant | MODIFIER | c.*973C>T| |
S173 |
9 | BAA08g12700 | A08 | 11102730 | G | A | downstream_gene_variant | MODIFIER | c.*1009G>A| |
S281 |
10 | BAA08g12700 | A08 | 11104347 | G | A | downstream_gene_variant | MODIFIER | c.*2626G>A| |
S133 |