Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12880 | A02 | 5760208 | C | T | missense_variant | MODERATE | c.2147G>A|p.Gly716Asp |
S112 |
2 | BAA02g12880 | A02 | 5760515 | G | A | missense_variant | MODERATE | c.1840C>T|p.Leu614Phe |
S288 |
3 | BAA02g12880 | A02 | 5761135 | C | T | synonymous_variant | LOW | c.1296G>A|p.Leu432Leu |
S299 |
4 | BAA02g12880 | A02 | 5761929 | G | A | missense_variant | MODERATE | c.667C>T|p.Pro223Ser |
S70 |
5 | BAA02g12880 | A02 | 5764735 | G | A | upstream_gene_variant | MODIFIER | c.-1302C>T| |
S209 |
6 | BAA02g12880 | A02 | 5765135 | C | T | upstream_gene_variant | MODIFIER | c.-1702G>A| |
S270 |
7 | BAA02g12880 | A02 | 5767105 | G | A | upstream_gene_variant | MODIFIER | c.-3672C>T| |
S238 |