Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11920 | A10 | 13478490 | G | A | downstream_gene_variant | MODIFIER | c.*4674C>T| |
S125 |
2 | BAA10g11920 | A10 | 13478977 | G | A | downstream_gene_variant | MODIFIER | c.*4187C>T| |
S240 |
3 | BAA10g11920 | A10 | 13479827 | G | A | downstream_gene_variant | MODIFIER | c.*3337C>T| |
S125 |
4 | BAA10g11920 | A10 | 13479833 | C | T | downstream_gene_variant | MODIFIER | c.*3331G>A| |
S40 S49 |
5 | BAA10g11920 | A10 | 13480762 | C | T | downstream_gene_variant | MODIFIER | c.*2402G>A| |
S25 |
6 | BAA10g11920 | A10 | 13481030 | C | T | downstream_gene_variant | MODIFIER | c.*2134G>A| |
S130 |
7 | BAA10g11920 | A10 | 13484243 | G | A | intron_variant | MODIFIER | c.96+165C>T| |
S138 |
8 | BAA10g11920 | A10 | 13488530 | C | T | upstream_gene_variant | MODIFIER | c.-4027G>A| |
S42 |
9 | BAA10g11920 | A10 | 13488716 | C | T | upstream_gene_variant | MODIFIER | c.-4213G>A| |
S173 |