| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 194951 | BAA02g28270 | A02 | 15892273 | G | A | upstream_gene_variant | MODIFIER | c.-1758C>T| |
S261 |
| 194952 | BAA02g28270 | A02 | 15892386 | C | T | upstream_gene_variant | MODIFIER | c.-1871G>A| |
S163 |
| 194953 | BAA02g28270 | A02 | 15892485 | G | A | upstream_gene_variant | MODIFIER | c.-1970C>T| |
S43 |
| 194954 | BAA02g28270 | A02 | 15893122 | C | T | upstream_gene_variant | MODIFIER | c.-2607G>A| |
S195 |
| 194955 | BAA02g28270 | A02 | 15893254 | C | T | upstream_gene_variant | MODIFIER | c.-2739G>A| |
S167 |
| 194956 | BAA02g28270 | A02 | 15893608 | C | T | upstream_gene_variant | MODIFIER | c.-3093G>A| |
S164 |
| 194957 | BAA02g28270 | A02 | 15893613 | G | A | upstream_gene_variant | MODIFIER | c.-3098C>T| |
S7 |
| 194958 | BAA02g28270 | A02 | 15894328 | G | A | upstream_gene_variant | MODIFIER | c.-3813C>T| |
S80 |
| 194959 | BAA02g28280 | A02 | 15895652 | G | A | upstream_gene_variant | MODIFIER | c.-2071C>T| |
S249 |
| 194960 | BAA02g28290 | A02 | 15895957 | C | T | missense_variant | MODERATE | c.139C>T|p.Leu47Phe |
S53 |
| 194961 | BAA02g28290 | A02 | 15896220 | C | T | synonymous_variant | LOW | c.402C>T|p.Phe134Phe |
S172 S217 |
| 194962 | BAA02g28280 | A02 | 15896915 | G | A | upstream_gene_variant | MODIFIER | c.-3334C>T| |
S292 |
| 194963 | BAA02g28300 | A02 | 15897085 | C | T | missense_variant | MODERATE | c.1171G>A|p.Ala391Thr |
S9 |
| 194964 | BAA02g28300 | A02 | 15897140 | G | A | synonymous_variant | LOW | c.1116C>T|p.Asp372Asp |
S34 |
| 194965 | BAA02g28300 | A02 | 15898001 | C | T | synonymous_variant | LOW | c.597G>A|p.Arg199Arg |
S305 |
| 194966 | BAA02g28300 | A02 | 15898747 | C | T | missense_variant&splice_region_variant | MODERATE | c.314G>A|p.Gly105Asp |
S178 |
| 194967 | BAA02g28300 | A02 | 15899554 | G | A | upstream_gene_variant | MODIFIER | c.-213C>T| |
S23 |
| 194968 | BAA02g28310 | A02 | 15900391 | A | C | missense_variant | MODERATE | c.1000T>G|p.Ser334Ala |
S273 |
| 194969 | BAA02g28310 | A02 | 15900595 | C | T | splice_region_variant&intron_variant | LOW | c.883+5G>A| |
S282 |
| 194970 | BAA02g28300 | A02 | 15901359 | G | A | upstream_gene_variant | MODIFIER | c.-2018C>T| |
S68 |
| 194971 | BAA02g28300 | A02 | 15902686 | A | T | upstream_gene_variant | MODIFIER | c.-3345T>A| |
S159 S243 |
| 194972 | BAA02g28300 | A02 | 15903174 | G | A | upstream_gene_variant | MODIFIER | c.-3833C>T| |
S247 |
| 194973 | BAA02g28310 | A02 | 15906028 | C | T | upstream_gene_variant | MODIFIER | c.-3864G>A| |
S162 |
| 194974 | BAA02g28310 | A02 | 15907082 | C | T | upstream_gene_variant | MODIFIER | c.-4918G>A| |
S63 |
| 194975 | BAA02g28320 | A02 | 15907357 | C | T | downstream_gene_variant | MODIFIER | c.*2889C>T| |
S273 |