| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 187101 | BAA02g24150 | A02 | 13158846 | C | T | downstream_gene_variant | MODIFIER | c.*525C>T| |
S87 |
| 187102 | BAA02g24150 | A02 | 13160227 | C | T | downstream_gene_variant | MODIFIER | c.*1906C>T| |
S1 S90 |
| 187103 | BAA02g24150 | A02 | 13160448 | C | T | downstream_gene_variant | MODIFIER | c.*2127C>T| |
S77 |
| 187104 | BAA02g24150 | A02 | 13161136 | G | A | downstream_gene_variant | MODIFIER | c.*2815G>A| |
S34 |
| 187105 | BAA02g24150 | A02 | 13161809 | G | A | downstream_gene_variant | MODIFIER | c.*3488G>A| |
S265 |
| 187106 | BAA02g24150 | A02 | 13163255 | C | T | downstream_gene_variant | MODIFIER | c.*4934C>T| |
S275 |
| 187107 | BAA02g24150-BAA02g24160 | A02 | 13164754 | C | T | intergenic_region | MODIFIER | n.13164754C>T| |
S276 |
| 187108 | BAA02g24160 | A02 | 13164901 | C | T | downstream_gene_variant | MODIFIER | c.*4962G>A| |
S5 |
| 187109 | BAA02g24160 | A02 | 13165671 | C | T | downstream_gene_variant | MODIFIER | c.*4192G>A| |
S271 |
| 187110 | BAA02g24160 | A02 | 13167245 | G | A | downstream_gene_variant | MODIFIER | c.*2618C>T| |
S37 |
| 187111 | BAA02g24160 | A02 | 13170481 | C | T | missense_variant | MODERATE | c.688G>A|p.Asp230Asn |
S192 |
| 187112 | BAA02g24160 | A02 | 13172807 | G | A | upstream_gene_variant | MODIFIER | c.-1384C>T| |
S288 |
| 187113 | BAA02g24160 | A02 | 13172831 | G | A | upstream_gene_variant | MODIFIER | c.-1408C>T| |
S38 |
| 187114 | BAA02g24160 | A02 | 13172997 | G | A | upstream_gene_variant | MODIFIER | c.-1574C>T| |
S20 |
| 187115 | BAA02g24160 | A02 | 13173354 | G | A | upstream_gene_variant | MODIFIER | c.-1931C>T| |
S146 |
| 187116 | BAA02g24170 | A02 | 13173973 | C | T | missense_variant | MODERATE | c.29C>T|p.Thr10Ile |
S296 |
| 187117 | BAA02g24170 | A02 | 13174088 | C | T | synonymous_variant | LOW | c.144C>T|p.Pro48Pro |
S221 |
| 187118 | BAA02g24170 | A02 | 13174091 | C | T | synonymous_variant | LOW | c.147C>T|p.Asn49Asn |
S80 |
| 187119 | BAA02g24160 | A02 | 13174664 | G | A | upstream_gene_variant | MODIFIER | c.-3241C>T| |
S183 S198 |
| 187120 | BAA02g24160 | A02 | 13174707 | C | T | upstream_gene_variant | MODIFIER | c.-3284G>A| |
S250 |
| 187121 | BAA02g24170 | A02 | 13175194 | C | T | synonymous_variant | LOW | c.904C>T|p.Leu302Leu |
S119 |
| 187122 | BAA02g24160 | A02 | 13176184 | C | T | upstream_gene_variant | MODIFIER | c.-4761G>A| |
S140 |
| 187123 | BAA02g24160 | A02 | 13176249 | G | A | upstream_gene_variant | MODIFIER | c.-4826C>T| |
S279 S67 |
| 187124 | BAA02g24180 | A02 | 13176326 | G | A | missense_variant | MODERATE | c.470C>T|p.Thr157Ile |
S156 |
| 187125 | BAA02g24180 | A02 | 13177617 | C | T | upstream_gene_variant | MODIFIER | c.-658G>A| |
S234 |