Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g33710 | A02 | 28839435 | C | T | missense_variant | MODERATE | c.2867G>A|p.Gly956Glu |
S48 |
2 | BAA02g33710 | A02 | 28839574 | C | T | missense_variant | MODERATE | c.2728G>A|p.Gly910Arg |
S183 S198 |
3 | BAA02g33710 | A02 | 28839998 | C | T | synonymous_variant | LOW | c.2304G>A|p.Gln768Gln |
S51 |
4 | BAA02g33710 | A02 | 28840535 | C | T | synonymous_variant | LOW | c.1767G>A|p.Glu589Glu |
S33 |
5 | BAA02g33710 | A02 | 28841447 | G | A | synonymous_variant | LOW | c.855C>T|p.Thr285Thr |
S251 |
6 | BAA02g33710 | A02 | 28841693 | G | A | synonymous_variant | LOW | c.609C>T|p.Phe203Phe |
S47 |
7 | BAA02g33710 | A02 | 28841758 | C | T | missense_variant | MODERATE | c.544G>A|p.Gly182Ser |
S189 |
8 | BAA02g33710 | A02 | 28841887 | G | A | stop_gained | HIGH | c.415C>T|p.Gln139* |
S136 |
9 | BAA02g33710 | A02 | 28843165 | G | A | upstream_gene_variant | MODIFIER | c.-864C>T| |
S288 |
10 | BAA02g33710 | A02 | 28843469 | G | A | upstream_gene_variant | MODIFIER | c.-1168C>T| |
S228 |
11 | BAA02g33710 | A02 | 28843527 | G | A | upstream_gene_variant | MODIFIER | c.-1226C>T| |
S288 |
12 | BAA02g33710 | A02 | 28844720 | G | A | upstream_gene_variant | MODIFIER | c.-2419C>T| |
S113 |
13 | BAA02g33710 | A02 | 28844956 | T | A | upstream_gene_variant | MODIFIER | c.-2655A>T| |
S18 |
14 | BAA02g33710 | A02 | 28845328 | G | A | upstream_gene_variant | MODIFIER | c.-3027C>T| |
S298 |
15 | BAA02g33710 | A02 | 28846491 | C | T | upstream_gene_variant | MODIFIER | c.-4190G>A| |
S219 S72 |