Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38530 | A02 | 32821446 | G | A | upstream_gene_variant | MODIFIER | c.-4783G>A| |
S291 |
2 | BAA02g38530 | A02 | 32822117 | G | A | upstream_gene_variant | MODIFIER | c.-4112G>A| |
S221 |
3 | BAA02g38530 | A02 | 32822164 | G | A | upstream_gene_variant | MODIFIER | c.-4065G>A| |
S132 S137 S215 S89 |
4 | BAA02g38530 | A02 | 32826415 | C | T | missense_variant | MODERATE | c.187C>T|p.Pro63Ser |
S168 |
5 | BAA02g38530 | A02 | 32826515 | A | C | missense_variant | MODERATE | c.287A>C|p.His96Pro |
S94 |
6 | BAA02g38530 | A02 | 32826758 | C | T | missense_variant | MODERATE | c.530C>T|p.Ser177Phe |
S255 |
7 | BAA02g38530 | A02 | 32827102 | T | C | missense_variant | MODERATE | c.874T>C|p.Phe292Leu |
S96 |
8 | BAA02g38530 | A02 | 32827107 | C | T | synonymous_variant | LOW | c.879C>T|p.Tyr293Tyr |
S48 |
9 | BAA02g38530 | A02 | 32827207 | G | A | missense_variant | MODERATE | c.979G>A|p.Asp327Asn |
S251 |
10 | BAA02g38530 | A02 | 32829547 | G | T | downstream_gene_variant | MODIFIER | c.*1957G>T| |
S149 |
11 | BAA02g38530 | A02 | 32829690 | G | A | downstream_gene_variant | MODIFIER | c.*2100G>A| |
S187 |
12 | BAA02g38530 | A02 | 32830367 | G | A | downstream_gene_variant | MODIFIER | c.*2777G>A| |
S279 |
13 | BAA02g38530 | A02 | 32830414 | C | T | downstream_gene_variant | MODIFIER | c.*2824C>T| |
S87 |
14 | BAA02g38530 | A02 | 32831133 | C | T | downstream_gene_variant | MODIFIER | c.*3543C>T| |
S208 S219 |
15 | BAA02g38530 | A02 | 32831890 | G | A | downstream_gene_variant | MODIFIER | c.*4300G>A| |
S279 |