Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13200 | A09 | 7578438 | G | A | missense_variant | MODERATE | c.355C>T|p.Leu119Phe |
S218 |
2 | BAA09g13200 | A09 | 7580104 | C | T | upstream_gene_variant | MODIFIER | c.-1100G>A| |
S71 |
3 | BAA09g13200 | A09 | 7580269 | C | T | upstream_gene_variant | MODIFIER | c.-1265G>A| |
S230 |
4 | BAA09g13200 | A09 | 7580953 | C | T | upstream_gene_variant | MODIFIER | c.-1949G>A| |
S8 |
5 | BAA09g13200 | A09 | 7581127 | C | T | upstream_gene_variant | MODIFIER | c.-2123G>A| |
S17 |
6 | BAA09g13200 | A09 | 7582822 | C | T | upstream_gene_variant | MODIFIER | c.-3818G>A| |
S17 |
7 | BAA09g13200 | A09 | 7583199 | G | A | upstream_gene_variant | MODIFIER | c.-4195C>T| |
S247 |