Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65970 | A09 | 60509511 | C | T | missense_variant | MODERATE | c.1768G>A|p.Asp590Asn |
S294 |
2 | BAA09g65970 | A09 | 60511736 | C | T | upstream_gene_variant | MODIFIER | c.-244G>A| |
S59 |
3 | BAA09g65970 | A09 | 60512502 | G | A | upstream_gene_variant | MODIFIER | c.-1010C>T| |
S166 |
4 | BAA09g65970 | A09 | 60512532 | G | A | upstream_gene_variant | MODIFIER | c.-1040C>T| |
S216 S241 S39 |
5 | BAA09g65970 | A09 | 60513023 | G | A | upstream_gene_variant | MODIFIER | c.-1531C>T| |
S291 |
6 | BAA09g65970 | A09 | 60514748 | G | A | upstream_gene_variant | MODIFIER | c.-3256C>T| |
S286 |
7 | BAA09g65970 | A09 | 60515631 | C | T | upstream_gene_variant | MODIFIER | c.-4139G>A| |
S292 |