Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18530 | A02 | 9439970 | C | T | stop_gained | HIGH | c.58C>T|p.Gln20* |
S283 |
2 | BAA02g18530 | A02 | 9440324 | C | T | splice_region_variant&synonymous_variant | LOW | c.208C>T|p.Leu70Leu |
S105 S106 |
3 | BAA02g18530 | A02 | 9442105 | C | A | missense_variant | MODERATE | c.1474C>A|p.Leu492Met |
S252 |
4 | BAA02g18530 | A02 | 9442107 | G | A | synonymous_variant | LOW | c.1476G>A|p.Leu492Leu |
S122 |
5 | BAA02g18530 | A02 | 9442304 | C | T | missense_variant | MODERATE | c.1673C>T|p.Ala558Val |
S124 |
6 | BAA02g18530 | A02 | 9442909 | C | T | missense_variant | MODERATE | c.2215C>T|p.Leu739Phe |
S6 |
7 | BAA02g18530 | A02 | 9444166 | G | A | downstream_gene_variant | MODIFIER | c.*1249G>A| |
S132 S137 S215 |
8 | BAA02g18530 | A02 | 9444774 | G | A | downstream_gene_variant | MODIFIER | c.*1857G>A| |
S202 |
9 | BAA02g18530 | A02 | 9445657 | C | T | downstream_gene_variant | MODIFIER | c.*2740C>T| |
S9 |
10 | BAA02g18530 | A02 | 9445792 | G | A | downstream_gene_variant | MODIFIER | c.*2875G>A| |
S43 |
11 | BAA02g18530 | A02 | 9446911 | G | A | downstream_gene_variant | MODIFIER | c.*3994G>A| |
S297 |