Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11000 | A01 | 5071434 | G | A | missense_variant | MODERATE | c.1237C>T|p.Pro413Ser |
S121 |
2 | BAA01g11000 | A01 | 5072104 | G | A | synonymous_variant | LOW | c.567C>T|p.Phe189Phe |
S133 |
3 | BAA01g11000 | A01 | 5073424 | G | A | upstream_gene_variant | MODIFIER | c.-754C>T| |
S122 |
4 | BAA01g11000 | A01 | 5074705 | G | A | upstream_gene_variant | MODIFIER | c.-2035C>T| |
S306 S308 |
5 | BAA01g11000 | A01 | 5075323 | G | A | upstream_gene_variant | MODIFIER | c.-2653C>T| |
S298 |
6 | BAA01g11000 | A01 | 5075402 | G | A | upstream_gene_variant | MODIFIER | c.-2732C>T| |
S259 |
7 | BAA01g11000 | A01 | 5075478 | G | A | upstream_gene_variant | MODIFIER | c.-2808C>T| |
S173 |
8 | BAA01g11000 | A01 | 5076575 | G | A | upstream_gene_variant | MODIFIER | c.-3905C>T| |
S176 S67 |