| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g15190 | A01 | 7279597 | C | T | upstream_gene_variant | MODIFIER | c.-3188C>T| |
S10 |
| 2 | BAA01g15190 | A01 | 7279848 | C | T | upstream_gene_variant | MODIFIER | c.-2937C>T| |
S247 |
| 3 | BAA01g15190 | A01 | 7279959 | G | A | upstream_gene_variant | MODIFIER | c.-2826G>A| |
S133 |
| 4 | BAA01g15190 | A01 | 7280873 | C | T | upstream_gene_variant | MODIFIER | c.-1912C>T| |
S249 |
| 5 | BAA01g15190 | A01 | 7281518 | G | A | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S174 S216 S241 S27 S39 |
| 6 | BAA01g15190 | A01 | 7282507 | G | A | upstream_gene_variant | MODIFIER | c.-278G>A| |
S238 |
| 7 | BAA01g15190 | A01 | 7282980 | G | A | missense_variant | MODERATE | c.196G>A|p.Asp66Asn |
S142 |
| 8 | BAA01g15190 | A01 | 7283268 | C | T | missense_variant | MODERATE | c.484C>T|p.Pro162Ser |
S159 S243 |
| 9 | BAA01g15190 | A01 | 7283774 | G | A | missense_variant | MODERATE | c.755G>A|p.Gly252Asp |
S9 |
| 10 | BAA01g15190 | A01 | 7283990 | G | A | stop_gained&splice_region_variant | HIGH | c.813G>A|p.Trp271* |
S229 |
| 11 | BAA01g15190 | A01 | 7286497 | C | T | downstream_gene_variant | MODIFIER | c.*2471C>T| |
S63 |
| 12 | BAA01g15190 | A01 | 7287009 | G | A | downstream_gene_variant | MODIFIER | c.*2983G>A| |
S209 |
| 13 | BAA01g15190 | A01 | 7287931 | C | T | downstream_gene_variant | MODIFIER | c.*3905C>T| |
S148 S30 S31 |
| 14 | BAA01g15190 | A01 | 7288338 | G | A | downstream_gene_variant | MODIFIER | c.*4312G>A| |
S115 |