Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g05840 | A09 | 3302825 | G | A | missense_variant | MODERATE | c.611G>A|p.Cys204Tyr |
S188 |
2 | BAA09g05840 | A09 | 3302990 | C | T | missense_variant | MODERATE | c.776C>T|p.Ala259Val |
S217 S248 |
3 | BAA09g05840 | A09 | 3303912 | C | T | missense_variant | MODERATE | c.1196C>T|p.Ala399Val |
S278 |
4 | BAA09g05840 | A09 | 3304110 | G | A | missense_variant | MODERATE | c.1318G>A|p.Glu440Lys |
S170 |
5 | BAA09g05840 | A09 | 3305446 | G | A | missense_variant | MODERATE | c.1961G>A|p.Arg654Lys |
S108 |
6 | BAA09g05840 | A09 | 3306240 | C | T | downstream_gene_variant | MODIFIER | c.*443C>T| |
S148 |
7 | BAA09g05840 | A09 | 3306689 | G | A | downstream_gene_variant | MODIFIER | c.*892G>A| |
S1 S90 |
8 | BAA09g05840 | A09 | 3306956 | C | T | downstream_gene_variant | MODIFIER | c.*1159C>T| |
S302 |
9 | BAA09g05840 | A09 | 3307415 | G | A | downstream_gene_variant | MODIFIER | c.*1618G>A| |
S308 |
10 | BAA09g05840 | A09 | 3308380 | G | A | downstream_gene_variant | MODIFIER | c.*2583G>A| |
S266 |
11 | BAA09g05840 | A09 | 3310618 | G | A | downstream_gene_variant | MODIFIER | c.*4821G>A| |
S289 S290 |