| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 167801 | BAA02g13430 | A02 | 6113729 | C | T | missense_variant | MODERATE | c.3014G>A|p.Gly1005Glu |
S289 S290 |
| 167802 | BAA02g13430 | A02 | 6116033 | C | T | missense_variant | MODERATE | c.2203G>A|p.Glu735Lys |
S135 |
| 167803 | BAA02g13430 | A02 | 6116158 | G | A | missense_variant | MODERATE | c.2078C>T|p.Ala693Val |
S282 |
| 167804 | BAA02g13420 | A02 | 6117249 | G | A | upstream_gene_variant | MODIFIER | c.-4590C>T| |
S244 |
| 167805 | BAA02g13420 | A02 | 6117455 | G | A | upstream_gene_variant | MODIFIER | c.-4796C>T| |
S168 |
| 167806 | BAA02g13420 | A02 | 6117487 | C | T | upstream_gene_variant | MODIFIER | c.-4828G>A| |
S1 S90 |
| 167807 | BAA02g13430 | A02 | 6117701 | C | T | intron_variant | MODIFIER | c.1392-769G>A| |
S289 S290 |
| 167808 | BAA02g13430 | A02 | 6118197 | G | A | intron_variant | MODIFIER | c.1391+842C>T| |
S59 |
| 167809 | BAA02g13430 | A02 | 6119126 | C | T | missense_variant | MODERATE | c.1304G>A|p.Arg435Gln |
S94 |
| 167810 | BAA02g13430 | A02 | 6119141 | A | C | missense_variant | MODERATE | c.1289T>G|p.Met430Arg |
S112 S178 |
| 167811 | BAA02g13430 | A02 | 6119566 | G | A | synonymous_variant | LOW | c.864C>T|p.Ser288Ser |
S271 |
| 167812 | BAA02g13430 | A02 | 6120018 | G | A | stop_gained | HIGH | c.412C>T|p.Gln138* |
S169 |
| 167813 | BAA02g13430 | A02 | 6122002 | C | T | upstream_gene_variant | MODIFIER | c.-1474G>A| |
S201 |
| 167814 | BAA02g13430 | A02 | 6122109 | C | T | upstream_gene_variant | MODIFIER | c.-1581G>A| |
S267 |
| 167815 | BAA02g13430 | A02 | 6122224 | G | A | upstream_gene_variant | MODIFIER | c.-1696C>T| |
S25 |
| 167816 | BAA02g13430 | A02 | 6123134 | C | T | upstream_gene_variant | MODIFIER | c.-2606G>A| |
S292 |
| 167817 | BAA02g13430 | A02 | 6123170 | G | A | upstream_gene_variant | MODIFIER | c.-2642C>T| |
S191 |
| 167818 | BAA02g13430-BAA02g13440 | A02 | 6125767 | C | T | intergenic_region | MODIFIER | n.6125767C>T| |
S216 |
| 167819 | BAA02g13430-BAA02g13440 | A02 | 6126152 | G | A | intergenic_region | MODIFIER | n.6126152G>A| |
S153 S213 |
| 167820 | BAA02g13430-BAA02g13440 | A02 | 6126704 | C | T | intergenic_region | MODIFIER | n.6126704C>T| |
S15 S3 |
| 167821 | BAA02g13430-BAA02g13440 | A02 | 6126834 | G | A | intergenic_region | MODIFIER | n.6126834G>A| |
S229 |
| 167822 | BAA02g13430-BAA02g13440 | A02 | 6126854 | G | A | intergenic_region | MODIFIER | n.6126854G>A| |
S193 |
| 167823 | BAA02g13430-BAA02g13440 | A02 | 6126870 | C | T | intergenic_region | MODIFIER | n.6126870C>T| |
S130 |
| 167824 | BAA02g13430-BAA02g13440 | A02 | 6127417 | C | T | intergenic_region | MODIFIER | n.6127417C>T| |
S103 |
| 167825 | BAA02g13430-BAA02g13440 | A02 | 6127620 | G | A | intergenic_region | MODIFIER | n.6127620G>A| |
S202 |