Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g01540 | A01 | 689036 | C | T | upstream_gene_variant | MODIFIER | c.-2188C>T| |
S38 |
2 | BAA01g01540 | A01 | 689686 | G | A | upstream_gene_variant | MODIFIER | c.-1538G>A| |
S12 |
3 | BAA01g01540 | A01 | 689834 | C | T | upstream_gene_variant | MODIFIER | c.-1390C>T| |
S120 |
4 | BAA01g01540 | A01 | 689956 | T | C | upstream_gene_variant | MODIFIER | c.-1268T>C| |
S66 |
5 | BAA01g01540 | A01 | 690348 | C | T | upstream_gene_variant | MODIFIER | c.-876C>T| |
S135 |
6 | BAA01g01540 | A01 | 690564 | G | A | upstream_gene_variant | MODIFIER | c.-660G>A| |
S17 |
7 | BAA01g01540 | A01 | 690784 | C | T | upstream_gene_variant | MODIFIER | c.-440C>T| |
S208 |
8 | BAA01g01540 | A01 | 691631 | C | T | synonymous_variant | LOW | c.408C>T|p.Leu136Leu |
S264 |
9 | BAA01g01540 | A01 | 691662 | C | T | missense_variant | MODERATE | c.439C>T|p.Leu147Phe |
S139 |
10 | BAA01g01540 | A01 | 692000 | G | A | synonymous_variant | LOW | c.777G>A|p.Glu259Glu |
S230 |
11 | BAA01g01540 | A01 | 693669 | C | T | synonymous_variant | LOW | c.1510C>T|p.Leu504Leu |
S134 |