Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47330 | A09 | 51668003 | C | T | downstream_gene_variant | MODIFIER | c.*4051G>A| |
S206 S26 |
2 | BAA09g47330 | A09 | 51669855 | G | A | downstream_gene_variant | MODIFIER | c.*2199C>T| |
S42 |
3 | BAA09g47330 | A09 | 51670282 | G | A | downstream_gene_variant | MODIFIER | c.*1772C>T| |
S38 |
4 | BAA09g47330 | A09 | 51670947 | G | A | downstream_gene_variant | MODIFIER | c.*1107C>T| |
S184 |
5 | BAA09g47330 | A09 | 51672075 | C | T | synonymous_variant | LOW | c.2523G>A|p.Lys841Lys |
S223 |
6 | BAA09g47330 | A09 | 51672228 | C | T | missense_variant | MODERATE | c.2471G>A|p.Gly824Glu |
S6 |
7 | BAA09g47330 | A09 | 51672255 | C | T | missense_variant | MODERATE | c.2444G>A|p.Gly815Glu |
S130 |
8 | BAA09g47330 | A09 | 51672990 | G | A | missense_variant | MODERATE | c.2069C>T|p.Pro690Leu |
S221 |
9 | BAA09g47330 | A09 | 51673008 | C | T | missense_variant | MODERATE | c.2051G>A|p.Gly684Glu |
S61 |
10 | BAA09g47330 | A09 | 51675459 | G | A | missense_variant | MODERATE | c.563C>T|p.Thr188Ile |
S236 |
11 | BAA09g47330 | A09 | 51678856 | C | T | upstream_gene_variant | MODIFIER | c.-2534G>A| |
S279 |
12 | BAA09g47330 | A09 | 51680080 | C | T | upstream_gene_variant | MODIFIER | c.-3758G>A| |
S297 |
13 | BAA09g47330 | A09 | 51680887 | C | T | upstream_gene_variant | MODIFIER | c.-4565G>A| |
S195 |
14 | BAA09g47330 | A09 | 51681050 | T | C | upstream_gene_variant | MODIFIER | c.-4728A>G| |
S181 |
15 | BAA09g47330 | A09 | 51681317 | G | A | upstream_gene_variant | MODIFIER | c.-4995C>T| |
S4 |