Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01400 | A09 | 1031569 | C | T | missense_variant | MODERATE | c.865G>A|p.Glu289Lys |
S150 |
2 | BAA09g01400 | A09 | 1031981 | G | A | synonymous_variant | LOW | c.579C>T|p.Leu193Leu |
S200 |
3 | BAA09g01400 | A09 | 1037097 | C | T | upstream_gene_variant | MODIFIER | c.-3775G>A| |
S247 |
4 | BAA09g01400 | A09 | 1037496 | G | A | upstream_gene_variant | MODIFIER | c.-4174C>T| |
S240 |
5 | BAA09g01400 | A09 | 1037520 | C | T | upstream_gene_variant | MODIFIER | c.-4198G>A| |
S270 |