| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 159651 | BAA02g07000 | A02 | 2998878 | G | A | upstream_gene_variant | MODIFIER | c.-2318C>T| |
S206 S26 |
| 159652 | BAA02g07000 | A02 | 2999865 | C | T | upstream_gene_variant | MODIFIER | c.-3305G>A| |
S250 |
| 159653 | BAA02g07000 | A02 | 3000015 | G | A | upstream_gene_variant | MODIFIER | c.-3455C>T| |
S126 |
| 159654 | BAA02g07000 | A02 | 3000041 | C | T | upstream_gene_variant | MODIFIER | c.-3481G>A| |
S174 S216 S39 |
| 159655 | BAA02g07000 | A02 | 3000466 | G | A | upstream_gene_variant | MODIFIER | c.-3906C>T| |
S177 |
| 159656 | BAA02g07000 | A02 | 3001346 | G | T | upstream_gene_variant | MODIFIER | c.-4786C>A| |
S164 |
| 159657 | BAA02g07010 | A02 | 3001846 | G | A | missense_variant | MODERATE | c.322G>A|p.Glu108Lys |
S256 |
| 159658 | BAA02g07020 | A02 | 3001987 | C | T | upstream_gene_variant | MODIFIER | c.-164C>T| |
S230 |
| 159659 | BAA02g07020 | A02 | 3002238 | G | A | missense_variant | MODERATE | c.88G>A|p.Ala30Thr |
S68 |
| 159660 | BAA02g07020 | A02 | 3002592 | C | T | missense_variant | MODERATE | c.442C>T|p.Leu148Phe |
S124 |
| 159661 | BAA02g07020 | A02 | 3002712 | G | A | missense_variant | MODERATE | c.562G>A|p.Val188Ile |
S64 |
| 159662 | BAA02g07030 | A02 | 3004017 | C | T | upstream_gene_variant | MODIFIER | c.-3195C>T| |
S257 |
| 159663 | BAA02g07030 | A02 | 3004210 | G | A | upstream_gene_variant | MODIFIER | c.-3002G>A| |
S143 |
| 159664 | BAA02g07030 | A02 | 3004247 | G | A | upstream_gene_variant | MODIFIER | c.-2965G>A| |
S61 |
| 159665 | BAA02g07030 | A02 | 3004760 | C | T | upstream_gene_variant | MODIFIER | c.-2452C>T| |
S277 |
| 159666 | BAA02g07030 | A02 | 3005225 | C | T | upstream_gene_variant | MODIFIER | c.-1987C>T| |
S19 |
| 159667 | BAA02g07030 | A02 | 3005589 | G | A | upstream_gene_variant | MODIFIER | c.-1623G>A| |
S288 |
| 159668 | BAA02g07030 | A02 | 3005853 | G | A | upstream_gene_variant | MODIFIER | c.-1359G>A| |
S61 |
| 159669 | BAA02g07030 | A02 | 3006064 | G | A | upstream_gene_variant | MODIFIER | c.-1148G>A| |
S139 |
| 159670 | BAA02g07030 | A02 | 3007291 | C | T | missense_variant | MODERATE | c.80C>T|p.Ser27Phe |
S240 |
| 159671 | BAA02g07030 | A02 | 3007349 | G | A | stop_gained | HIGH | c.138G>A|p.Trp46* |
S110 |
| 159672 | BAA02g07030 | A02 | 3007454 | C | T | synonymous_variant | LOW | c.243C>T|p.Ile81Ile |
S123 |
| 159673 | BAA02g07030 | A02 | 3008475 | C | T | intron_variant | MODIFIER | c.1249+15C>T| |
S230 |
| 159674 | BAA02g07030 | A02 | 3008494 | G | A | intron_variant | MODIFIER | c.1249+34G>A| |
S89 |
| 159675 | BAA02g07030 | A02 | 3010274 | G | A | downstream_gene_variant | MODIFIER | c.*941G>A| |
S237 |