Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00270 | A01 | 128052 | G | A | missense_variant | MODERATE | c.1315C>T|p.Pro439Ser |
S152 |
2 | BAA01g00270 | A01 | 129042 | G | A | missense_variant | MODERATE | c.664C>T|p.His222Tyr |
S262 |
3 | BAA01g00270 | A01 | 129065 | G | A | missense_variant | MODERATE | c.641C>T|p.Ser214Phe |
S11 |
4 | BAA01g00270 | A01 | 132822 | G | A | upstream_gene_variant | MODIFIER | c.-2609C>T| |
S5 |
5 | BAA01g00270 | A01 | 133870 | G | A | upstream_gene_variant | MODIFIER | c.-3657C>T| |
S11 |
6 | BAA01g00270 | A01 | 135135 | G | A | upstream_gene_variant | MODIFIER | c.-4922C>T| |
S105 S106 |