Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46690 | A09 | 51336379 | C | T | missense_variant | MODERATE | c.902G>A|p.Gly301Asp |
S230 |
2 | BAA09g46690 | A09 | 51336754 | C | T | missense_variant | MODERATE | c.527G>A|p.Arg176Lys |
S272 |
3 | BAA09g46690 | A09 | 51336833 | G | A | missense_variant | MODERATE | c.448C>T|p.Arg150Cys |
S135 |
4 | BAA09g46690 | A09 | 51336959 | G | A | missense_variant | MODERATE | c.322C>T|p.Leu108Phe |
S105 S106 |
5 | BAA09g46690 | A09 | 51339324 | G | A | upstream_gene_variant | MODIFIER | c.-2044C>T| |
S161 |
6 | BAA09g46690 | A09 | 51339379 | G | A | upstream_gene_variant | MODIFIER | c.-2099C>T| |
S69 |
7 | BAA09g46690 | A09 | 51339421 | G | A | upstream_gene_variant | MODIFIER | c.-2141C>T| |
S72 S78 |
8 | BAA09g46690 | A09 | 51340331 | C | T | upstream_gene_variant | MODIFIER | c.-3051G>A| |
S211 S227 |
9 | BAA09g46690 | A09 | 51340802 | G | A | upstream_gene_variant | MODIFIER | c.-3522C>T| |
S69 |
10 | BAA09g46690 | A09 | 51340858 | C | T | upstream_gene_variant | MODIFIER | c.-3578G>A| |
S297 |
11 | BAA09g46690 | A09 | 51342269 | G | A | upstream_gene_variant | MODIFIER | c.-4989C>T| |
S17 |