Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59470 | A09 | 57580467 | C | T | upstream_gene_variant | MODIFIER | c.-16C>T| |
S168 |
2 | BAA09g59470 | A09 | 57580586 | G | A | missense_variant | MODERATE | c.104G>A|p.Cys35Tyr |
S262 |
3 | BAA09g59470 | A09 | 57580648 | G | A | missense_variant | MODERATE | c.166G>A|p.Asp56Asn |
S197 |
4 | BAA09g59470 | A09 | 57580709 | C | T | missense_variant | MODERATE | c.227C>T|p.Thr76Ile |
S278 |
5 | BAA09g59470 | A09 | 57580715 | G | A | missense_variant | MODERATE | c.233G>A|p.Gly78Glu |
S247 |
6 | BAA09g59470 | A09 | 57581353 | C | T | synonymous_variant | LOW | c.528C>T|p.Ile176Ile |
S28 |
7 | BAA09g59470 | A09 | 57581616 | G | A | missense_variant | MODERATE | c.791G>A|p.Ser264Asn |
S280 |
8 | BAA09g59470 | A09 | 57585982 | G | A | downstream_gene_variant | MODIFIER | c.*4344G>A| |
S63 |