| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157701 | BAA02g05340 | A02 | 2331033 | G | A | synonymous_variant | LOW | c.903C>T|p.Thr301Thr |
S126 |
| 157702 | BAA02g05340 | A02 | 2332314 | C | T | upstream_gene_variant | MODIFIER | c.-284G>A| |
S159 S187 S188 S243 S276 S299 |
| 157703 | BAA02g05340 | A02 | 2332377 | G | A | upstream_gene_variant | MODIFIER | c.-347C>T| |
S265 |
| 157704 | BAA02g05340 | A02 | 2333139 | C | T | upstream_gene_variant | MODIFIER | c.-1109G>A| |
S116 |
| 157705 | BAA02g05340 | A02 | 2333442 | G | A | upstream_gene_variant | MODIFIER | c.-1412C>T| |
S247 |
| 157706 | BAA02g05340 | A02 | 2333887 | C | T | upstream_gene_variant | MODIFIER | c.-1857G>A| |
S1 S90 |
| 157707 | BAA02g05350 | A02 | 2334078 | C | T | missense_variant | MODERATE | c.52C>T|p.His18Tyr |
S219 S72 |
| 157708 | BAA02g05350 | A02 | 2334713 | C | T | missense_variant | MODERATE | c.530C>T|p.Thr177Ile |
S87 |
| 157709 | BAA02g05350 | A02 | 2334926 | C | T | missense_variant | MODERATE | c.743C>T|p.Ser248Phe |
S263 |
| 157710 | BAA02g05350 | A02 | 2336067 | C | T | missense_variant | MODERATE | c.1589C>T|p.Thr530Ile |
S183 S198 |
| 157711 | BAA02g05340 | A02 | 2336353 | C | T | upstream_gene_variant | MODIFIER | c.-4323G>A| |
S182 |
| 157712 | BAA02g05340 | A02 | 2336565 | C | T | upstream_gene_variant | MODIFIER | c.-4535G>A| |
S46 |
| 157713 | BAA02g05350 | A02 | 2337318 | C | T | downstream_gene_variant | MODIFIER | c.*1157C>T| |
S274 |
| 157714 | BAA02g05360 | A02 | 2338156 | G | A | upstream_gene_variant | MODIFIER | c.-57C>T| |
S34 |
| 157715 | BAA02g05360 | A02 | 2340564 | G | A | upstream_gene_variant | MODIFIER | c.-2465C>T| |
S139 |
| 157716 | BAA02g05380 | A02 | 2343085 | G | A | synonymous_variant | LOW | c.375G>A|p.Gln125Gln |
S204 |
| 157717 | BAA02g05370 | A02 | 2343265 | G | A | upstream_gene_variant | MODIFIER | c.-2850C>T| |
S110 |
| 157718 | BAA02g05380 | A02 | 2344158 | C | T | missense_variant | MODERATE | c.745C>T|p.Pro249Ser |
S160 |
| 157719 | BAA02g05380 | A02 | 2344695 | G | A | missense_variant | MODERATE | c.1114G>A|p.Gly372Ser |
S266 |
| 157720 | BAA02g05380 | A02 | 2345864 | G | A | synonymous_variant | LOW | c.1602G>A|p.Lys534Lys |
S202 |
| 157721 | BAA02g05380 | A02 | 2345877 | C | T | missense_variant | MODERATE | c.1615C>T|p.Pro539Ser |
S275 |
| 157722 | BAA02g05380 | A02 | 2345968 | G | A | missense_variant | MODERATE | c.1706G>A|p.Gly569Glu |
S17 |
| 157723 | BAA02g05380 | A02 | 2346005 | G | A | missense_variant | MODERATE | c.1743G>A|p.Met581Ile |
S10 |
| 157724 | BAA02g05400 | A02 | 2347527 | G | A | upstream_gene_variant | MODIFIER | c.-3565G>A| |
S210 S225 |
| 157725 | BAA02g05390 | A02 | 2348090 | G | A | synonymous_variant | LOW | c.588G>A|p.Glu196Glu |
S190 |