Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g60600 | A09 | 58089723 | G | A | upstream_gene_variant | MODIFIER | c.-2944G>A| |
S187 |
2 | BAA09g60600 | A09 | 58092757 | C | T | missense_variant | MODERATE | c.91C>T|p.Pro31Ser |
S156 |
3 | BAA09g60600 | A09 | 58092803 | C | T | missense_variant | MODERATE | c.137C>T|p.Pro46Leu |
S136 |
4 | BAA09g60600 | A09 | 58092976 | C | T | missense_variant | MODERATE | c.310C>T|p.Pro104Ser |
S201 |
5 | BAA09g60600 | A09 | 58093695 | G | A | missense_variant | MODERATE | c.755G>A|p.Arg252Lys |
S274 |
6 | BAA09g60600 | A09 | 58094188 | C | T | splice_region_variant&synonymous_variant | LOW | c.789C>T|p.Val263Val |
S168 |
7 | BAA09g60600 | A09 | 58094421 | C | T | missense_variant | MODERATE | c.1022C>T|p.Ser341Phe |
S13 |
8 | BAA09g60600 | A09 | 58094486 | C | T | stop_gained | HIGH | c.1087C>T|p.Gln363* |
S265 |