Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11180 | A01 | 5165157 | G | A | missense_variant | MODERATE | c.2222C>T|p.Pro741Leu |
S172 S217 |
2 | BAA01g11180 | A01 | 5165419 | G | A | missense_variant | MODERATE | c.1960C>T|p.Pro654Ser |
S224 |
3 | BAA01g11180 | A01 | 5166326 | G | A | synonymous_variant | LOW | c.1053C>T|p.Phe351Phe |
S8 |
4 | BAA01g11180 | A01 | 5166433 | C | T | missense_variant | MODERATE | c.946G>A|p.Val316Ile |
S230 |
5 | BAA01g11180 | A01 | 5166520 | C | T | missense_variant | MODERATE | c.859G>A|p.Glu287Lys |
S170 |
6 | BAA01g11180 | A01 | 5166673 | C | T | missense_variant | MODERATE | c.706G>A|p.Glu236Lys |
S182 |
7 | BAA01g11180 | A01 | 5167987 | C | T | upstream_gene_variant | MODIFIER | c.-609G>A| |
S255 |
8 | BAA01g11180 | A01 | 5168059 | C | T | upstream_gene_variant | MODIFIER | c.-681G>A| |
S18 |
9 | BAA01g11180 | A01 | 5168646 | G | A | upstream_gene_variant | MODIFIER | c.-1268C>T| |
S209 |
10 | BAA01g11180 | A01 | 5168929 | G | A | upstream_gene_variant | MODIFIER | c.-1551C>T| |
S274 |
11 | BAA01g11180 | A01 | 5169158 | C | T | upstream_gene_variant | MODIFIER | c.-1780G>A| |
S242 |
12 | BAA01g11180 | A01 | 5170359 | C | T | upstream_gene_variant | MODIFIER | c.-2981G>A| |
S125 |
13 | BAA01g11180 | A01 | 5171516 | G | A | upstream_gene_variant | MODIFIER | c.-4138C>T| |
S274 |
14 | BAA01g11180 | A01 | 5171914 | C | T | upstream_gene_variant | MODIFIER | c.-4536G>A| |
S249 |