| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 170401 | BAA02g15060-BAA02g15070 | A02 | 7187172 | C | T | intergenic_region | MODIFIER | n.7187172C>T| |
S75 S81 |
| 170402 | BAA02g15070 | A02 | 7189954 | G | A | upstream_gene_variant | MODIFIER | c.-3930G>A| |
S69 |
| 170403 | BAA02g15070 | A02 | 7191458 | C | T | upstream_gene_variant | MODIFIER | c.-2426C>T| |
S38 |
| 170404 | BAA02g15070 | A02 | 7191625 | G | A | upstream_gene_variant | MODIFIER | c.-2259G>A| |
S228 |
| 170405 | BAA02g15070 | A02 | 7191805 | G | A | upstream_gene_variant | MODIFIER | c.-2079G>A| |
S159 S243 |
| 170406 | BAA02g15070 | A02 | 7191920 | G | A | upstream_gene_variant | MODIFIER | c.-1964G>A| |
S149 |
| 170407 | BAA02g15070 | A02 | 7192443 | G | A | upstream_gene_variant | MODIFIER | c.-1441G>A| |
S296 |
| 170408 | BAA02g15080 | A02 | 7194754 | T | C | downstream_gene_variant | MODIFIER | c.*4883A>G| |
S221 |
| 170409 | BAA02g15080 | A02 | 7195699 | C | T | downstream_gene_variant | MODIFIER | c.*3938G>A| |
S180 |
| 170410 | BAA02g15070 | A02 | 7196573 | C | T | synonymous_variant | LOW | c.1563C>T|p.Arg521Arg |
S216 |
| 170411 | BAA02g15070 | A02 | 7196949 | G | A | missense_variant | MODERATE | c.1763G>A|p.Arg588Lys |
S62 |
| 170412 | BAA02g15080 | A02 | 7197019 | G | A | downstream_gene_variant | MODIFIER | c.*2618C>T| |
S281 |
| 170413 | BAA02g15070 | A02 | 7197140 | C | T | synonymous_variant | LOW | c.1881C>T|p.Ile627Ile |
S183 S198 |
| 170414 | BAA02g15080 | A02 | 7197245 | C | T | downstream_gene_variant | MODIFIER | c.*2392G>A| |
S270 |
| 170415 | BAA02g15070 | A02 | 7197976 | G | A | missense_variant | MODERATE | c.2444G>A|p.Gly815Glu |
S251 |
| 170416 | BAA02g15070 | A02 | 7198796 | G | A | missense_variant | MODERATE | c.3019G>A|p.Glu1007Lys |
S281 |
| 170417 | BAA02g15070 | A02 | 7198815 | G | A | missense_variant | MODERATE | c.3038G>A|p.Arg1013Lys |
S298 |
| 170418 | BAA02g15070 | A02 | 7199074 | C | T | missense_variant | MODERATE | c.3215C>T|p.Ser1072Leu |
S112 |
| 170419 | BAA02g15070 | A02 | 7199292 | G | A | missense_variant | MODERATE | c.3433G>A|p.Val1145Ile |
S148 S210 S30 S31 |
| 170420 | BAA02g15070 | A02 | 7199301 | G | A | missense_variant | MODERATE | c.3442G>A|p.Glu1148Lys |
S209 |
| 170421 | BAA02g15070 | A02 | 7199322 | C | T | stop_gained | HIGH | c.3463C>T|p.Gln1155* |
S100 |
| 170422 | BAA02g15080 | A02 | 7201299 | C | T | upstream_gene_variant | MODIFIER | c.-806G>A| |
S105 S106 |
| 170423 | BAA02g15080 | A02 | 7202125 | G | A | upstream_gene_variant | MODIFIER | c.-1632C>T| |
S139 |
| 170424 | BAA02g15080 | A02 | 7204024 | T | C | upstream_gene_variant | MODIFIER | c.-3531A>G| |
S149 |
| 170425 | BAA02g15080 | A02 | 7204186 | C | T | upstream_gene_variant | MODIFIER | c.-3693G>A| |
S224 |