Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65660 | A09 | 60382133 | G | A | missense_variant | MODERATE | c.812C>T|p.Pro271Leu |
S189 |
2 | BAA09g65660 | A09 | 60384958 | C | T | upstream_gene_variant | MODIFIER | c.-1815G>A| |
S131 |
3 | BAA09g65660 | A09 | 60386647 | G | A | upstream_gene_variant | MODIFIER | c.-3504C>T| |
S291 |
4 | BAA09g65660 | A09 | 60387340 | C | T | upstream_gene_variant | MODIFIER | c.-4197G>A| |
S153 S213 |
5 | BAA09g65660 | A09 | 60387674 | C | T | upstream_gene_variant | MODIFIER | c.-4531G>A| |
S67 |
6 | BAA09g65660 | A09 | 60387857 | C | T | upstream_gene_variant | MODIFIER | c.-4714G>A| |
S27 |