Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45430 | A09 | 50629292 | G | A | downstream_gene_variant | MODIFIER | c.*2161C>T| |
S90 |
2 | BAA09g45430 | A09 | 50631290 | C | T | downstream_gene_variant | MODIFIER | c.*163G>A| |
S211 S227 |
3 | BAA09g45430 | A09 | 50631570 | C | T | synonymous_variant | LOW | c.777G>A|p.Ala259Ala |
S144 |
4 | BAA09g45430 | A09 | 50632241 | C | T | stop_gained | HIGH | c.345G>A|p.Trp115* |
S261 |
5 | BAA09g45430 | A09 | 50632272 | C | T | missense_variant | MODERATE | c.314G>A|p.Arg105Lys |
S206 S26 |
6 | BAA09g45430 | A09 | 50632752 | C | T | missense_variant | MODERATE | c.142G>A|p.Val48Ile |
S192 |
7 | BAA09g45430 | A09 | 50632761 | G | A | missense_variant | MODERATE | c.133C>T|p.Pro45Ser |
S172 S217 |
8 | BAA09g45430 | A09 | 50632988 | C | T | upstream_gene_variant | MODIFIER | c.-15G>A| |
S179 |
9 | BAA09g45430 | A09 | 50633662 | G | A | upstream_gene_variant | MODIFIER | c.-689C>T| |
S11 |
10 | BAA09g45430 | A09 | 50633742 | C | T | upstream_gene_variant | MODIFIER | c.-769G>A| |
S115 |
11 | BAA09g45430 | A09 | 50633989 | C | T | upstream_gene_variant | MODIFIER | c.-1016G>A| |
S249 S43 |
12 | BAA09g45430 | A09 | 50634314 | C | T | upstream_gene_variant | MODIFIER | c.-1341G>A| |
S163 |
13 | BAA09g45430 | A09 | 50635548 | G | A | upstream_gene_variant | MODIFIER | c.-2575C>T| |
S244 |