Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g09010 | A09 | 5026332 | G | A | upstream_gene_variant | MODIFIER | c.-2142G>A| |
S236 |
2 | BAA09g09010 | A09 | 5026797 | G | A | upstream_gene_variant | MODIFIER | c.-1677G>A| |
S36 |
3 | BAA09g09010 | A09 | 5026798 | C | T | upstream_gene_variant | MODIFIER | c.-1676C>T| |
S117 |
4 | BAA09g09010 | A09 | 5027025 | C | T | upstream_gene_variant | MODIFIER | c.-1449C>T| |
S104 S52 |
5 | BAA09g09010 | A09 | 5027195 | C | T | upstream_gene_variant | MODIFIER | c.-1279C>T| |
S28 |
6 | BAA09g09010 | A09 | 5027545 | C | T | upstream_gene_variant | MODIFIER | c.-929C>T| |
S247 |
7 | BAA09g09010 | A09 | 5028448 | G | A | upstream_gene_variant | MODIFIER | c.-26G>A| |
S152 |
8 | BAA09g09010 | A09 | 5028883 | C | T | missense_variant | MODERATE | c.410C>T|p.Ser137Phe |
S305 |
9 | BAA09g09010 | A09 | 5030300 | C | T | missense_variant | MODERATE | c.971C>T|p.Thr324Ile |
S257 |