Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g30770 | A06 | 20942619 | C | A | upstream_gene_variant | MODIFIER | c.-4753C>A| |
S53 |
2 | BAA06g30770 | A06 | 20942717 | G | A | upstream_gene_variant | MODIFIER | c.-4655G>A| |
S40 S49 |
3 | BAA06g30770 | A06 | 20943127 | C | T | upstream_gene_variant | MODIFIER | c.-4245C>T| |
S280 |
4 | BAA06g30770 | A06 | 20943562 | G | A | upstream_gene_variant | MODIFIER | c.-3810G>A| |
S5 |
5 | BAA06g30770 | A06 | 20944778 | C | T | upstream_gene_variant | MODIFIER | c.-2594C>T| |
S242 |
6 | BAA06g30770 | A06 | 20945511 | G | A | upstream_gene_variant | MODIFIER | c.-1861G>A| |
S39 |
7 | BAA06g30770 | A06 | 20946244 | G | A | upstream_gene_variant | MODIFIER | c.-1128G>A| |
S161 S228 |
8 | BAA06g30770 | A06 | 20946334 | G | A | upstream_gene_variant | MODIFIER | c.-1038G>A| |
S94 |
9 | BAA06g30770 | A06 | 20946520 | C | T | upstream_gene_variant | MODIFIER | c.-852C>T| |
S9 |
10 | BAA06g30770 | A06 | 20948661 | C | T | intron_variant | MODIFIER | c.964+326C>T| |
S7 |
11 | BAA06g30770 | A06 | 20948792 | G | A | intron_variant | MODIFIER | c.964+457G>A| |
S235 |