| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 155151 | BAA02g03300 | A02 | 1470143 | G | A | upstream_gene_variant | MODIFIER | c.-4476C>T| |
S36 |
| 155152 | BAA02g03300 | A02 | 1470483 | C | A | upstream_gene_variant | MODIFIER | c.-4816G>T| |
S126 |
| 155153 | BAA02g03300 | A02 | 1470569 | C | T | upstream_gene_variant | MODIFIER | c.-4902G>A| |
S34 |
| 155154 | BAA02g03330 | A02 | 1471716 | C | T | missense_variant | MODERATE | c.740G>A|p.Arg247Lys |
S280 |
| 155155 | BAA02g03310 | A02 | 1472620 | G | A | upstream_gene_variant | MODIFIER | c.-4972C>T| |
S68 |
| 155156 | BAA02g03330 | A02 | 1472969 | G | A | missense_variant | MODERATE | c.209C>T|p.Ser70Phe |
S60 |
| 155157 | BAA02g03320 | A02 | 1473527 | G | A | upstream_gene_variant | MODIFIER | c.-3730C>T| |
S239 |
| 155158 | BAA02g03320 | A02 | 1473567 | G | A | upstream_gene_variant | MODIFIER | c.-3770C>T| |
S237 |
| 155159 | BAA02g03330 | A02 | 1475660 | G | A | upstream_gene_variant | MODIFIER | c.-2483C>T| |
S237 |
| 155160 | BAA02g03340 | A02 | 1476675 | G | A | missense_variant | MODERATE | c.545C>T|p.Pro182Leu |
S84 S93 |
| 155161 | BAA02g03330 | A02 | 1478065 | C | T | upstream_gene_variant | MODIFIER | c.-4888G>A| |
S185 |
| 155162 | BAA02g03340 | A02 | 1479661 | C | T | upstream_gene_variant | MODIFIER | c.-2442G>A| |
S159 S187 S188 S243 S276 S299 |
| 155163 | BAA02g03340 | A02 | 1479814 | C | T | upstream_gene_variant | MODIFIER | c.-2595G>A| |
S251 |
| 155164 | BAA02g03340 | A02 | 1480374 | G | A | upstream_gene_variant | MODIFIER | c.-3155C>T| |
S114 |
| 155165 | BAA02g03340 | A02 | 1480763 | C | T | upstream_gene_variant | MODIFIER | c.-3544G>A| |
S298 |
| 155166 | BAA02g03350 | A02 | 1482060 | C | T | synonymous_variant | LOW | c.21C>T|p.Leu7Leu |
S71 |
| 155167 | BAA02g03350 | A02 | 1482433 | C | T | missense_variant | MODERATE | c.394C>T|p.Leu132Phe |
S186 |
| 155168 | BAA02g03350 | A02 | 1484028 | C | T | missense_variant | MODERATE | c.1487C>T|p.Pro496Leu |
S42 |
| 155169 | BAA02g03350 | A02 | 1484109 | C | T | missense_variant | MODERATE | c.1568C>T|p.Ser523Phe |
S250 |
| 155170 | BAA02g03350 | A02 | 1484806 | G | A | downstream_gene_variant | MODIFIER | c.*588G>A| |
S23 |
| 155171 | BAA02g03350 | A02 | 1484900 | G | A | downstream_gene_variant | MODIFIER | c.*682G>A| |
S206 S26 |
| 155172 | BAA02g03370 | A02 | 1485321 | C | T | upstream_gene_variant | MODIFIER | c.-4768C>T| |
S85 |
| 155173 | BAA02g03360 | A02 | 1486348 | G | A | synonymous_variant | LOW | c.924C>T|p.Leu308Leu |
S139 |
| 155174 | BAA02g03360 | A02 | 1486593 | C | T | missense_variant | MODERATE | c.746G>A|p.Arg249Gln |
S40 S49 |
| 155175 | BAA02g03370 | A02 | 1486995 | C | T | upstream_gene_variant | MODIFIER | c.-3094C>T| |
S251 |