Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09870 | A01 | 4423570 | C | T | missense_variant | MODERATE | c.2695G>A|p.Glu899Lys |
S25 |
2 | BAA01g09870 | A01 | 4424360 | C | T | missense_variant | MODERATE | c.1990G>A|p.Ala664Thr |
S135 |
3 | BAA01g09870 | A01 | 4424633 | C | T | missense_variant | MODERATE | c.1717G>A|p.Val573Ile |
S295 |
4 | BAA01g09870 | A01 | 4424795 | G | A | missense_variant | MODERATE | c.1555C>T|p.Arg519Cys |
S281 |
5 | BAA01g09870 | A01 | 4424811 | C | T | synonymous_variant | LOW | c.1539G>A|p.Glu513Glu |
S169 |
6 | BAA01g09870 | A01 | 4426447 | G | A | upstream_gene_variant | MODIFIER | c.-98C>T| |
S296 |
7 | BAA01g09870 | A01 | 4426653 | G | A | upstream_gene_variant | MODIFIER | c.-304C>T| |
S293 |
8 | BAA01g09870 | A01 | 4427421 | G | A | upstream_gene_variant | MODIFIER | c.-1072C>T| |
S10 |
9 | BAA01g09870 | A01 | 4430547 | C | T | upstream_gene_variant | MODIFIER | c.-4198G>A| |
S179 |
10 | BAA01g09870 | A01 | 4430862 | C | T | upstream_gene_variant | MODIFIER | c.-4513G>A| |
S282 |
11 | BAA01g09870 | A01 | 4431224 | G | A | upstream_gene_variant | MODIFIER | c.-4875C>T| |
S202 |