Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20490 | A10 | 18416457 | G | A | upstream_gene_variant | MODIFIER | c.-3920G>A| |
S85 |
2 | BAA10g20490 | A10 | 18416538 | G | A | upstream_gene_variant | MODIFIER | c.-3839G>A| |
S75 S81 |
3 | BAA10g20490 | A10 | 18416674 | G | A | upstream_gene_variant | MODIFIER | c.-3703G>A| |
S9 |
4 | BAA10g20490 | A10 | 18416718 | C | T | upstream_gene_variant | MODIFIER | c.-3659C>T| |
S23 |
5 | BAA10g20490 | A10 | 18418510 | G | A | upstream_gene_variant | MODIFIER | c.-1867G>A| |
S191 |
6 | BAA10g20490 | A10 | 18418679 | C | T | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S199 |
7 | BAA10g20490 | A10 | 18420029 | C | T | upstream_gene_variant | MODIFIER | c.-348C>T| |
S221 |
8 | BAA10g20490 | A10 | 18421686 | A | C | downstream_gene_variant | MODIFIER | c.*581A>C| |
S92 |
9 | BAA10g20490 | A10 | 18422201 | C | T | downstream_gene_variant | MODIFIER | c.*1096C>T| |
S152 |
10 | BAA10g20490 | A10 | 18422270 | C | T | downstream_gene_variant | MODIFIER | c.*1165C>T| |
S148 S30 S31 |