| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 174101 | BAA02g17070 | A02 | 8503371 | G | A | missense_variant | MODERATE | c.35C>T|p.Ser12Phe |
S177 |
| 174102 | BAA02g17070 | A02 | 8503626 | G | A | upstream_gene_variant | MODIFIER | c.-221C>T| |
S166 |
| 174103 | BAA02g17070 | A02 | 8504461 | C | T | upstream_gene_variant | MODIFIER | c.-1056G>A| |
S32 |
| 174104 | BAA02g17070 | A02 | 8506048 | C | T | upstream_gene_variant | MODIFIER | c.-2643G>A| |
S208 S219 |
| 174105 | BAA02g17070 | A02 | 8506892 | G | A | upstream_gene_variant | MODIFIER | c.-3487C>T| |
S69 |
| 174106 | BAA02g17070 | A02 | 8508197 | C | T | upstream_gene_variant | MODIFIER | c.-4792G>A| |
S70 |
| 174107 | BAA02g17080 | A02 | 8509025 | G | A | upstream_gene_variant | MODIFIER | c.-520G>A| |
S153 S213 |
| 174108 | BAA02g17080 | A02 | 8509433 | G | A | upstream_gene_variant | MODIFIER | c.-112G>A| |
S296 |
| 174109 | BAA02g17090 | A02 | 8509952 | C | T | downstream_gene_variant | MODIFIER | c.*1707G>A| |
S186 |
| 174110 | BAA02g17080 | A02 | 8510105 | C | T | missense_variant | MODERATE | c.271C>T|p.Pro91Ser |
S18 |
| 174111 | BAA02g17080 | A02 | 8511177 | G | A | downstream_gene_variant | MODIFIER | c.*1043G>A| |
S122 |
| 174112 | BAA02g17080 | A02 | 8511363 | G | A | downstream_gene_variant | MODIFIER | c.*1229G>A| |
S150 |
| 174113 | BAA02g17090 | A02 | 8513455 | C | T | upstream_gene_variant | MODIFIER | c.-753G>A| |
S13 |
| 174114 | BAA02g17090 | A02 | 8513691 | G | A | upstream_gene_variant | MODIFIER | c.-989C>T| |
S297 |
| 174115 | BAA02g17090 | A02 | 8515776 | G | A | upstream_gene_variant | MODIFIER | c.-3074C>T| |
S265 |
| 174116 | BAA02g17090 | A02 | 8516291 | C | T | upstream_gene_variant | MODIFIER | c.-3589G>A| |
S87 |
| 174117 | BAA02g17090 | A02 | 8516770 | G | A | upstream_gene_variant | MODIFIER | c.-4068C>T| |
S291 |
| 174118 | BAA02g17100 | A02 | 8517793 | T | A | upstream_gene_variant | MODIFIER | c.-2516T>A| |
S181 |
| 174119 | BAA02g17100 | A02 | 8518185 | G | A | upstream_gene_variant | MODIFIER | c.-2124G>A| |
S28 S298 |
| 174120 | BAA02g17100 | A02 | 8520339 | G | A | missense_variant | MODERATE | c.31G>A|p.Asp11Asn |
S278 |
| 174121 | BAA02g17100 | A02 | 8521443 | C | T | synonymous_variant | LOW | c.510C>T|p.His170His |
S275 |
| 174122 | BAA02g17110 | A02 | 8521965 | C | T | downstream_gene_variant | MODIFIER | c.*1030G>A| |
S84 S93 |
| 174123 | BAA02g17110 | A02 | 8525505 | C | T | upstream_gene_variant | MODIFIER | c.-318G>A| |
S273 |
| 174124 | BAA02g17110 | A02 | 8525741 | C | T | upstream_gene_variant | MODIFIER | c.-554G>A| |
S177 S245 |
| 174125 | BAA02g17110 | A02 | 8525978 | C | T | upstream_gene_variant | MODIFIER | c.-791G>A| |
S202 |