Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01120 | A02 | 531765 | C | T | missense_variant | MODERATE | c.1858G>A|p.Asp620Asn |
S83 S88 |
2 | BAA02g01120 | A02 | 532756 | A | G | synonymous_variant | LOW | c.867T>C|p.Leu289Leu |
S142 |
3 | BAA02g01120 | A02 | 533080 | C | T | synonymous_variant | LOW | c.543G>A|p.Val181Val |
S112 |
4 | BAA02g01120 | A02 | 533392 | G | A | synonymous_variant | LOW | c.231C>T|p.Phe77Phe |
S153 S213 |
5 | BAA02g01120 | A02 | 533894 | G | A | upstream_gene_variant | MODIFIER | c.-272C>T| |
S162 |
6 | BAA02g01120 | A02 | 535052 | C | T | upstream_gene_variant | MODIFIER | c.-1430G>A| |
S177 |
7 | BAA02g01120 | A02 | 535358 | G | A | upstream_gene_variant | MODIFIER | c.-1736C>T| |
S238 |
8 | BAA02g01120 | A02 | 535530 | G | A | upstream_gene_variant | MODIFIER | c.-1908C>T| |
S292 |
9 | BAA02g01120 | A02 | 536689 | G | A | upstream_gene_variant | MODIFIER | c.-3067C>T| |
S166 |
10 | BAA02g01120 | A02 | 537769 | G | A | upstream_gene_variant | MODIFIER | c.-4147C>T| |
S41 |
11 | BAA02g01120 | A02 | 538364 | C | T | upstream_gene_variant | MODIFIER | c.-4742G>A| |
S135 |