Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13600 | A02 | 6302702 | G | A | upstream_gene_variant | MODIFIER | c.-2203G>A| |
S168 |
2 | BAA02g13600 | A02 | 6305814 | C | T | missense_variant | MODERATE | c.472C>T|p.Pro158Ser |
S94 |
3 | BAA02g13600 | A02 | 6306012 | C | T | missense_variant | MODERATE | c.575C>T|p.Pro192Leu |
S283 |
4 | BAA02g13600 | A02 | 6306293 | C | T | missense_variant | MODERATE | c.769C>T|p.Pro257Ser |
S81 |
5 | BAA02g13600 | A02 | 6306543 | C | T | missense_variant | MODERATE | c.935C>T|p.Pro312Leu |
S255 |
6 | BAA02g13600 | A02 | 6306843 | C | T | stop_gained | HIGH | c.1156C>T|p.Gln386* |
S200 |
7 | BAA02g13600 | A02 | 6306882 | C | T | missense_variant | MODERATE | c.1195C>T|p.Leu399Phe |
S1 S90 |
8 | BAA02g13600 | A02 | 6306890 | C | T | synonymous_variant | LOW | c.1203C>T|p.Asp401Asp |
S221 |
9 | BAA02g13600 | A02 | 6307232 | G | A | synonymous_variant | LOW | c.1545G>A|p.Gly515Gly |
S237 |
10 | BAA02g13600 | A02 | 6307298 | G | A | synonymous_variant | LOW | c.1611G>A|p.Lys537Lys |
S25 |
11 | BAA02g13600 | A02 | 6308041 | G | A | intron_variant | MODIFIER | c.2008+209G>A| |
S218 S267 S268 S269 |
12 | BAA02g13600 | A02 | 6314224 | G | A | synonymous_variant | LOW | c.2388G>A|p.Glu796Glu |
S263 |
13 | BAA02g13600 | A02 | 6314239 | G | A | stop_gained | HIGH | c.2403G>A|p.Trp801* |
S59 |
14 | BAA02g13600 | A02 | 6314895 | C | T | downstream_gene_variant | MODIFIER | c.*128C>T| |
S103 |
15 | BAA02g13600 | A02 | 6318500 | G | A | downstream_gene_variant | MODIFIER | c.*3733G>A| |
S295 |
16 | BAA02g13600 | A02 | 6318717 | G | A | downstream_gene_variant | MODIFIER | c.*3950G>A| |
S289 S290 |
17 | BAA02g13600 | A02 | 6318932 | G | A | downstream_gene_variant | MODIFIER | c.*4165G>A| |
S190 |