| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 174401 | BAA02g17280 | A02 | 8608167 | C | T | missense_variant | MODERATE | c.1130C>T|p.Ala377Val |
S9 |
| 174402 | BAA02g17280 | A02 | 8609721 | C | T | downstream_gene_variant | MODIFIER | c.*509C>T| |
S94 |
| 174403 | BAA02g17290 | A02 | 8610050 | G | A | upstream_gene_variant | MODIFIER | c.-4934G>A| |
S153 S213 |
| 174404 | BAA02g17290 | A02 | 8611662 | C | T | upstream_gene_variant | MODIFIER | c.-3322C>T| |
S63 |
| 174405 | BAA02g17290 | A02 | 8611784 | G | A | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S240 |
| 174406 | BAA02g17290 | A02 | 8611847 | G | A | upstream_gene_variant | MODIFIER | c.-3137G>A| |
S240 |
| 174407 | BAA02g17290 | A02 | 8612669 | C | T | upstream_gene_variant | MODIFIER | c.-2315C>T| |
S88 |
| 174408 | BAA02g17290 | A02 | 8612812 | G | A | upstream_gene_variant | MODIFIER | c.-2172G>A| |
S223 |
| 174409 | BAA02g17290 | A02 | 8612821 | C | T | upstream_gene_variant | MODIFIER | c.-2163C>T| |
S144 |
| 174410 | BAA02g17290 | A02 | 8613078 | G | A | upstream_gene_variant | MODIFIER | c.-1906G>A| |
S187 |
| 174411 | BAA02g17290 | A02 | 8613413 | G | A | upstream_gene_variant | MODIFIER | c.-1571G>A| |
S202 |
| 174412 | BAA02g17290 | A02 | 8615650 | C | T | missense_variant | MODERATE | c.401C>T|p.Pro134Leu |
S160 |
| 174413 | BAA02g17290 | A02 | 8616645 | C | T | missense_variant | MODERATE | c.863C>T|p.Pro288Leu |
S200 |
| 174414 | BAA02g17300 | A02 | 8616790 | G | A | upstream_gene_variant | MODIFIER | c.-3756G>A| |
S81 S85 |
| 174415 | BAA02g17290 | A02 | 8617026 | G | A | missense_variant | MODERATE | c.1000G>A|p.Asp334Asn |
S303 |
| 174416 | BAA02g17300 | A02 | 8618544 | G | A | upstream_gene_variant | MODIFIER | c.-2002G>A| |
S183 |
| 174417 | BAA02g17300 | A02 | 8619339 | C | T | upstream_gene_variant | MODIFIER | c.-1207C>T| |
S284 |
| 174418 | BAA02g17300 | A02 | 8619834 | G | A | upstream_gene_variant | MODIFIER | c.-712G>A| |
S237 |
| 174419 | BAA02g17300 | A02 | 8620668 | G | A | synonymous_variant | LOW | c.123G>A|p.Pro41Pro |
S116 |
| 174420 | BAA02g17290 | A02 | 8620939 | G | A | downstream_gene_variant | MODIFIER | c.*2649G>A| |
S20 |
| 174421 | BAA02g17300 | A02 | 8621307 | G | A | missense_variant | MODERATE | c.590G>A|p.Arg197Lys |
S187 |
| 174422 | BAA02g17300 | A02 | 8621857 | C | T | synonymous_variant | LOW | c.1140C>T|p.Phe380Phe |
S233 |
| 174423 | BAA02g17310 | A02 | 8623187 | C | T | upstream_gene_variant | MODIFIER | c.-3153C>T| |
S179 |
| 174424 | BAA02g17310 | A02 | 8624512 | G | A | upstream_gene_variant | MODIFIER | c.-1828G>A| |
S303 |
| 174425 | BAA02g17310 | A02 | 8625332 | C | T | upstream_gene_variant | MODIFIER | c.-1008C>T| |
S81 S85 |