Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g47770 | A03 | 22921571 | G | A | missense_variant | MODERATE | c.211G>A|p.Glu71Lys |
S261 |
2 | BAA03g47770 | A03 | 22924218 | C | T | missense_variant | MODERATE | c.368C>T|p.Thr123Ile |
S206 S26 |
3 | BAA03g47770 | A03 | 22924341 | C | T | missense_variant | MODERATE | c.491C>T|p.Ser164Phe |
S206 S26 |
4 | BAA03g47770 | A03 | 22924704 | C | T | missense_variant | MODERATE | c.854C>T|p.Pro285Leu |
S2 |
5 | BAA03g47770 | A03 | 22927476 | G | T | downstream_gene_variant | MODIFIER | c.*1976G>T| |
S145 S195 S221 S230 S247 S33 |
6 | BAA03g47770 | A03 | 22927647 | C | T | downstream_gene_variant | MODIFIER | c.*2147C>T| |
S142 |
7 | BAA03g47770 | A03 | 22928067 | C | T | downstream_gene_variant | MODIFIER | c.*2567C>T| |
S183 S198 |
8 | BAA03g47770 | A03 | 22928549 | C | T | downstream_gene_variant | MODIFIER | c.*3049C>T| |
S108 |
9 | BAA03g47770 | A03 | 22928567 | G | A | downstream_gene_variant | MODIFIER | c.*3067G>A| |
S56 |
10 | BAA03g47770 | A03 | 22928606 | G | A | downstream_gene_variant | MODIFIER | c.*3106G>A| |
S109 |
11 | BAA03g47770 | A03 | 22929758 | G | A | downstream_gene_variant | MODIFIER | c.*4258G>A| |
S6 |