Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34160 | A02 | 29289902 | C | T | splice_region_variant&intron_variant | LOW | c.1307+5G>A| |
S104 S52 |
2 | BAA02g34160 | A02 | 29290120 | G | A | missense_variant | MODERATE | c.1094C>T|p.Pro365Leu |
S25 |
3 | BAA02g34160 | A02 | 29290121 | G | A | missense_variant | MODERATE | c.1093C>T|p.Pro365Ser |
S114 |
4 | BAA02g34160 | A02 | 29291465 | G | A | missense_variant | MODERATE | c.119C>T|p.Pro40Leu |
S148 S210 S30 S31 |
5 | BAA02g34160 | A02 | 29292164 | G | A | upstream_gene_variant | MODIFIER | c.-581C>T| |
S306 S308 |
6 | BAA02g34160 | A02 | 29292304 | C | T | upstream_gene_variant | MODIFIER | c.-721G>A| |
S100 |
7 | BAA02g34160 | A02 | 29293347 | G | A | upstream_gene_variant | MODIFIER | c.-1764C>T| |
S136 |
8 | BAA02g34160 | A02 | 29293539 | G | A | upstream_gene_variant | MODIFIER | c.-1956C>T| |
S25 |
9 | BAA02g34160 | A02 | 29293548 | C | T | upstream_gene_variant | MODIFIER | c.-1965G>A| |
S75 |
10 | BAA02g34160 | A02 | 29293580 | C | T | upstream_gene_variant | MODIFIER | c.-1997G>A| |
S162 |
11 | BAA02g34160 | A02 | 29294061 | G | A | upstream_gene_variant | MODIFIER | c.-2478C>T| |
S142 |
12 | BAA02g34160 | A02 | 29294413 | G | A | upstream_gene_variant | MODIFIER | c.-2830C>T| |
S136 |
13 | BAA02g34160 | A02 | 29294817 | C | T | upstream_gene_variant | MODIFIER | c.-3234G>A| |
S195 |
14 | BAA02g34160 | A02 | 29295222 | G | A | upstream_gene_variant | MODIFIER | c.-3639C>T| |
S17 |
15 | BAA02g34160 | A02 | 29295441 | G | A | upstream_gene_variant | MODIFIER | c.-3858C>T| |
S188 |
16 | BAA02g34160 | A02 | 29295499 | G | A | upstream_gene_variant | MODIFIER | c.-3916C>T| |
S37 |
17 | BAA02g34160 | A02 | 29295616 | G | A | upstream_gene_variant | MODIFIER | c.-4033C>T| |
S245 |