Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g34070 | A09 | 42594917 | G | A | missense_variant | MODERATE | c.1747C>T|p.Leu583Phe |
S133 |
2 | BAA09g34070 | A09 | 42594932 | G | A | missense_variant | MODERATE | c.1732C>T|p.His578Tyr |
S20 |
3 | BAA09g34070 | A09 | 42595099 | C | T | missense_variant | MODERATE | c.1565G>A|p.Gly522Glu |
S237 |
4 | BAA09g34070 | A09 | 42596282 | C | T | missense_variant | MODERATE | c.382G>A|p.Glu128Lys |
S245 |
5 | BAA09g34070 | A09 | 42596463 | C | T | synonymous_variant | LOW | c.201G>A|p.Glu67Glu |
S68 |
6 | BAA09g34070 | A09 | 42598077 | G | A | upstream_gene_variant | MODIFIER | c.-1414C>T| |
S176 |
7 | BAA09g34070 | A09 | 42600467 | G | A | upstream_gene_variant | MODIFIER | c.-3804C>T| |
S238 |
8 | BAA09g34070 | A09 | 42601091 | G | A | upstream_gene_variant | MODIFIER | c.-4428C>T| |
S17 |
9 | BAA09g34070 | A09 | 42601407 | G | A | upstream_gene_variant | MODIFIER | c.-4744C>T| |
S16 |