Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68930 | A09 | 61767431 | C | T | missense_variant | MODERATE | c.2056G>A|p.Val686Met |
S67 |
2 | BAA09g68930 | A09 | 61768221 | G | A | synonymous_variant | LOW | c.1446C>T|p.Asp482Asp |
S247 |
3 | BAA09g68930 | A09 | 61768996 | G | A | missense_variant | MODERATE | c.1009C>T|p.Leu337Phe |
S39 |
4 | BAA09g68930 | A09 | 61769357 | G | A | synonymous_variant | LOW | c.648C>T|p.Ile216Ile |
S116 |
5 | BAA09g68930 | A09 | 61770141 | G | A | synonymous_variant | LOW | c.33C>T|p.Thr11Thr |
S195 |
6 | BAA09g68930 | A09 | 61770705 | G | A | upstream_gene_variant | MODIFIER | c.-532C>T| |
S2 S276 |
7 | BAA09g68930 | A09 | 61771529 | G | A | upstream_gene_variant | MODIFIER | c.-1356C>T| |
S288 |
8 | BAA09g68930 | A09 | 61773156 | C | T | upstream_gene_variant | MODIFIER | c.-2983G>A| |
S155 |
9 | BAA09g68930 | A09 | 61773642 | C | T | upstream_gene_variant | MODIFIER | c.-3469G>A| |
S242 |