Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49640 | A09 | 52867741 | G | A | downstream_gene_variant | MODIFIER | c.*3799C>T| |
S270 |
2 | BAA09g49640 | A09 | 52867836 | C | T | downstream_gene_variant | MODIFIER | c.*3704G>A| |
S170 |
3 | BAA09g49640 | A09 | 52867898 | G | A | downstream_gene_variant | MODIFIER | c.*3642C>T| |
S262 |
4 | BAA09g49640 | A09 | 52869728 | C | T | downstream_gene_variant | MODIFIER | c.*1812G>A| |
S95 |
5 | BAA09g49640 | A09 | 52872726 | G | A | intron_variant | MODIFIER | c.1321-329C>T| |
S161 |
6 | BAA09g49640 | A09 | 52873333 | C | T | intron_variant | MODIFIER | c.1321-936G>A| |
S192 |
7 | BAA09g49640 | A09 | 52873746 | G | A | intron_variant | MODIFIER | c.1321-1349C>T| |
S283 |
8 | BAA09g49640 | A09 | 52874342 | C | T | intron_variant | MODIFIER | c.1321-1945G>A| |
S296 |
9 | BAA09g49640 | A09 | 52875698 | C | T | intron_variant | MODIFIER | c.1320+3204G>A| |
S13 |
10 | BAA09g49640 | A09 | 52875970 | G | A | intron_variant | MODIFIER | c.1320+2932C>T| |
S42 |
11 | BAA09g49640 | A09 | 52881646 | G | A | upstream_gene_variant | MODIFIER | c.-105C>T| |
S284 |