Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46720 | A01 | 31145766 | G | A | missense_variant | MODERATE | c.85C>T|p.Pro29Ser |
S259 |
2 | BAA01g46720 | A01 | 31145964 | C | T | upstream_gene_variant | MODIFIER | c.-114G>A| |
S256 |
3 | BAA01g46720 | A01 | 31146617 | G | A | upstream_gene_variant | MODIFIER | c.-767C>T| |
S244 |
4 | BAA01g46720 | A01 | 31146672 | G | A | upstream_gene_variant | MODIFIER | c.-822C>T| |
S152 |
5 | BAA01g46720 | A01 | 31146772 | G | A | upstream_gene_variant | MODIFIER | c.-922C>T| |
S223 |
6 | BAA01g46720 | A01 | 31146956 | C | T | upstream_gene_variant | MODIFIER | c.-1106G>A| |
S8 |
7 | BAA01g46720 | A01 | 31148334 | G | A | upstream_gene_variant | MODIFIER | c.-2484C>T| |
S202 |
8 | BAA01g46720 | A01 | 31148516 | C | T | upstream_gene_variant | MODIFIER | c.-2666G>A| |
S200 |
9 | BAA01g46720 | A01 | 31148624 | C | T | upstream_gene_variant | MODIFIER | c.-2774G>A| |
S16 |
10 | BAA01g46720 | A01 | 31149124 | C | T | upstream_gene_variant | MODIFIER | c.-3274G>A| |
S166 |
11 | BAA01g46720 | A01 | 31149623 | C | T | upstream_gene_variant | MODIFIER | c.-3773G>A| |
S239 |
12 | BAA01g46720 | A01 | 31150663 | C | T | upstream_gene_variant | MODIFIER | c.-4813G>A| |
S153 S213 |