Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00160 | A08 | 110649 | G | A | missense_variant | MODERATE | c.244C>T|p.Leu82Phe |
S208 |
2 | BAA08g00160 | A08 | 114777 | G | A | upstream_gene_variant | MODIFIER | c.-3229C>T| |
S199 |
3 | BAA08g00160 | A08 | 115170 | G | A | upstream_gene_variant | MODIFIER | c.-3622C>T| |
S124 |
4 | BAA08g00160 | A08 | 115296 | C | T | upstream_gene_variant | MODIFIER | c.-3748G>A| |
S162 |
5 | BAA08g00160 | A08 | 115727 | G | A | upstream_gene_variant | MODIFIER | c.-4179C>T| |
S87 |
6 | BAA08g00160 | A08 | 116065 | C | T | upstream_gene_variant | MODIFIER | c.-4517G>A| |
S163 |
7 | BAA08g00160 | A08 | 116254 | C | T | upstream_gene_variant | MODIFIER | c.-4706G>A| |
S7 |