Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g03500 | A09 | 2091284 | G | A | upstream_gene_variant | MODIFIER | c.-1795G>A| |
S205 |
2 | BAA09g03500 | A09 | 2091447 | C | T | upstream_gene_variant | MODIFIER | c.-1632C>T| |
S244 |
3 | BAA09g03500 | A09 | 2091924 | G | A | upstream_gene_variant | MODIFIER | c.-1155G>A| |
S273 |
4 | BAA09g03500 | A09 | 2092155 | G | A | upstream_gene_variant | MODIFIER | c.-924G>A| |
S16 |
5 | BAA09g03500 | A09 | 2092635 | G | A | upstream_gene_variant | MODIFIER | c.-444G>A| |
S225 S73 |
6 | BAA09g03500 | A09 | 2093055 | G | A | upstream_gene_variant | MODIFIER | c.-24G>A| |
S23 |
7 | BAA09g03500 | A09 | 2093124 | G | A | missense_variant | MODERATE | c.46G>A|p.Ala16Thr |
S200 |
8 | BAA09g03500 | A09 | 2093147 | C | T | synonymous_variant | LOW | c.69C>T|p.Leu23Leu |
S239 |
9 | BAA09g03500 | A09 | 2093488 | G | A | missense_variant | MODERATE | c.152G>A|p.Gly51Glu |
S283 |
10 | BAA09g03500 | A09 | 2093514 | C | T | missense_variant | MODERATE | c.178C>T|p.Pro60Ser |
S211 S227 |
11 | BAA09g03500 | A09 | 2093841 | G | A | missense_variant | MODERATE | c.505G>A|p.Gly169Ser |
S108 |