Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15070 | A02 | 7189954 | G | A | upstream_gene_variant | MODIFIER | c.-3930G>A| |
S69 |
2 | BAA02g15070 | A02 | 7191458 | C | T | upstream_gene_variant | MODIFIER | c.-2426C>T| |
S38 |
3 | BAA02g15070 | A02 | 7191625 | G | A | upstream_gene_variant | MODIFIER | c.-2259G>A| |
S228 |
4 | BAA02g15070 | A02 | 7191805 | G | A | upstream_gene_variant | MODIFIER | c.-2079G>A| |
S159 S243 |
5 | BAA02g15070 | A02 | 7191920 | G | A | upstream_gene_variant | MODIFIER | c.-1964G>A| |
S149 |
6 | BAA02g15070 | A02 | 7192443 | G | A | upstream_gene_variant | MODIFIER | c.-1441G>A| |
S296 |
7 | BAA02g15070 | A02 | 7196573 | C | T | synonymous_variant | LOW | c.1563C>T|p.Arg521Arg |
S216 |
8 | BAA02g15070 | A02 | 7196949 | G | A | missense_variant | MODERATE | c.1763G>A|p.Arg588Lys |
S62 |
9 | BAA02g15070 | A02 | 7197140 | C | T | synonymous_variant | LOW | c.1881C>T|p.Ile627Ile |
S183 S198 |
10 | BAA02g15070 | A02 | 7197976 | G | A | missense_variant | MODERATE | c.2444G>A|p.Gly815Glu |
S251 |
11 | BAA02g15070 | A02 | 7198796 | G | A | missense_variant | MODERATE | c.3019G>A|p.Glu1007Lys |
S281 |
12 | BAA02g15070 | A02 | 7198815 | G | A | missense_variant | MODERATE | c.3038G>A|p.Arg1013Lys |
S298 |
13 | BAA02g15070 | A02 | 7199074 | C | T | missense_variant | MODERATE | c.3215C>T|p.Ser1072Leu |
S112 |
14 | BAA02g15070 | A02 | 7199292 | G | A | missense_variant | MODERATE | c.3433G>A|p.Val1145Ile |
S148 S210 S30 S31 |
15 | BAA02g15070 | A02 | 7199301 | G | A | missense_variant | MODERATE | c.3442G>A|p.Glu1148Lys |
S209 |
16 | BAA02g15070 | A02 | 7199322 | C | T | stop_gained | HIGH | c.3463C>T|p.Gln1155* |
S100 |