Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10160 | A09 | 5601998 | C | T | upstream_gene_variant | MODIFIER | c.-3265C>T| |
S202 |
2 | BAA09g10160 | A09 | 5602381 | G | A | upstream_gene_variant | MODIFIER | c.-2882G>A| |
S178 |
3 | BAA09g10160 | A09 | 5602908 | G | A | upstream_gene_variant | MODIFIER | c.-2355G>A| |
S159 S299 |
4 | BAA09g10160 | A09 | 5603285 | G | A | upstream_gene_variant | MODIFIER | c.-1978G>A| |
S228 |
5 | BAA09g10160 | A09 | 5603583 | G | A | upstream_gene_variant | MODIFIER | c.-1680G>A| |
S142 |
6 | BAA09g10160 | A09 | 5603700 | G | A | upstream_gene_variant | MODIFIER | c.-1563G>A| |
S306 S308 |
7 | BAA09g10160 | A09 | 5604440 | C | T | upstream_gene_variant | MODIFIER | c.-823C>T| |
S156 |
8 | BAA09g10160 | A09 | 5604912 | C | T | upstream_gene_variant | MODIFIER | c.-351C>T| |
S17 S59 |
9 | BAA09g10160 | A09 | 5605713 | C | T | synonymous_variant | LOW | c.367C>T|p.Leu123Leu |
S104 S52 |
10 | BAA09g10160 | A09 | 5606308 | C | T | missense_variant | MODERATE | c.638C>T|p.Ser213Leu |
S302 |
11 | BAA09g10160 | A09 | 5606325 | C | T | missense_variant | MODERATE | c.655C>T|p.Pro219Ser |
S33 |
12 | BAA09g10160 | A09 | 5606335 | C | T | missense_variant | MODERATE | c.665C>T|p.Thr222Ile |
S280 |
13 | BAA09g10160 | A09 | 5606706 | C | T | synonymous_variant | LOW | c.774C>T|p.Val258Val |
S135 S203 S68 |
14 | BAA09g10160 | A09 | 5607106 | G | A | missense_variant | MODERATE | c.902G>A|p.Gly301Glu |
S57 |