| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 163251 | BAA02g10050 | A02 | 4435666 | C | T | missense_variant | MODERATE | c.1669C>T|p.Leu557Phe |
S204 |
| 163252 | BAA02g10040 | A02 | 4435750 | C | T | upstream_gene_variant | MODIFIER | c.-4694G>A| |
S65 |
| 163253 | BAA02g10060 | A02 | 4436636 | G | A | downstream_gene_variant | MODIFIER | c.*2403C>T| |
S52 |
| 163254 | BAA02g10060 | A02 | 4437423 | G | A | downstream_gene_variant | MODIFIER | c.*1616C>T| |
S170 |
| 163255 | BAA02g10050 | A02 | 4437871 | G | A | downstream_gene_variant | MODIFIER | c.*164G>A| |
S148 S210 S30 S31 |
| 163256 | BAA02g10050 | A02 | 4438020 | C | T | downstream_gene_variant | MODIFIER | c.*313C>T| |
S185 |
| 163257 | BAA02g10050 | A02 | 4439021 | C | T | downstream_gene_variant | MODIFIER | c.*1314C>T| |
S280 |
| 163258 | BAA02g10060 | A02 | 4439872 | G | A | synonymous_variant | LOW | c.1942C>T|p.Leu648Leu |
S275 |
| 163259 | BAA02g10060 | A02 | 4440125 | G | A | synonymous_variant | LOW | c.1785C>T|p.Ser595Ser |
S126 |
| 163260 | BAA02g10060 | A02 | 4440670 | G | A | missense_variant | MODERATE | c.1406C>T|p.Thr469Ile |
S274 |
| 163261 | BAA02g10060 | A02 | 4441442 | C | T | missense_variant&splice_region_variant | MODERATE | c.937G>A|p.Val313Ile |
S116 |
| 163262 | BAA02g10060 | A02 | 4441581 | G | A | missense_variant | MODERATE | c.908C>T|p.Pro303Leu |
S197 |
| 163263 | BAA02g10070 | A02 | 4441665 | C | T | upstream_gene_variant | MODIFIER | c.-4020C>T| |
S117 |
| 163264 | BAA02g10070 | A02 | 4441673 | G | A | upstream_gene_variant | MODIFIER | c.-4012G>A| |
S67 |
| 163265 | BAA02g10060 | A02 | 4441917 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.689-1G>A| |
S119 |
| 163266 | BAA02g10060 | A02 | 4443537 | C | T | upstream_gene_variant | MODIFIER | c.-678G>A| |
S79 S84 |
| 163267 | BAA02g10060 | A02 | 4443788 | G | A | upstream_gene_variant | MODIFIER | c.-929C>T| |
S223 |
| 163268 | BAA02g10060 | A02 | 4445512 | C | T | upstream_gene_variant | MODIFIER | c.-2653G>A| |
S167 |
| 163269 | BAA02g10070 | A02 | 4445820 | G | A | missense_variant | MODERATE | c.136G>A|p.Gly46Ser |
S52 |
| 163270 | BAA02g10060 | A02 | 4446035 | G | C | upstream_gene_variant | MODIFIER | c.-3176C>G| |
S193 |
| 163271 | BAA02g10060 | A02 | 4446411 | C | T | upstream_gene_variant | MODIFIER | c.-3552G>A| |
S42 |
| 163272 | BAA02g10060 | A02 | 4446564 | C | T | upstream_gene_variant | MODIFIER | c.-3705G>A| |
S117 |
| 163273 | BAA02g10060 | A02 | 4447190 | C | T | upstream_gene_variant | MODIFIER | c.-4331G>A| |
S189 |
| 163274 | BAA02g10070 | A02 | 4447348 | G | A | missense_variant | MODERATE | c.673G>A|p.Asp225Asn |
S261 |
| 163275 | BAA02g10070 | A02 | 4447468 | G | A | missense_variant | MODERATE | c.793G>A|p.Glu265Lys |
S188 |