| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g18500 | A05 | 10631534 | C | T | upstream_gene_variant | MODIFIER | c.-4522C>T| |
S38 |
| 2 | BAA05g18500 | A05 | 10632503 | C | T | upstream_gene_variant | MODIFIER | c.-3553C>T| |
S8 |
| 3 | BAA05g18500 | A05 | 10632864 | C | T | upstream_gene_variant | MODIFIER | c.-3192C>T| |
S262 |
| 4 | BAA05g18500 | A05 | 10634773 | C | T | upstream_gene_variant | MODIFIER | c.-1283C>T| |
S237 |
| 5 | BAA05g18500 | A05 | 10635855 | G | A | upstream_gene_variant | MODIFIER | c.-201G>A| |
S266 |
| 6 | BAA05g18500 | A05 | 10636309 | C | T | missense_variant | MODERATE | c.254C>T|p.Pro85Leu |
S240 |
| 7 | BAA05g18500 | A05 | 10637261 | G | A | splice_region_variant&intron_variant | LOW | c.910-6G>A| |
S120 |
| 8 | BAA05g18500 | A05 | 10637677 | G | A | missense_variant&splice_region_variant | MODERATE | c.1231G>A|p.Asp411Asn |
S25 |
| 9 | BAA05g18500 | A05 | 10638008 | C | T | missense_variant | MODERATE | c.1562C>T|p.Ser521Phe |
S256 |
| 10 | BAA05g18500 | A05 | 10640224 | C | T | downstream_gene_variant | MODIFIER | c.*2164C>T| |
S256 |
| 11 | BAA05g18500 | A05 | 10640785 | C | T | downstream_gene_variant | MODIFIER | c.*2725C>T| |
S133 |
| 12 | BAA05g18500 | A05 | 10642315 | G | A | downstream_gene_variant | MODIFIER | c.*4255G>A| |
S15 |
| 13 | BAA05g18500 | A05 | 10642335 | G | A | downstream_gene_variant | MODIFIER | c.*4275G>A| |
S174 S241 S39 |