| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 195451 | BAA02g28540 | A02 | 16047504 | C | T | missense_variant | MODERATE | c.118C>T|p.Pro40Ser |
S293 |
| 195452 | BAA02g28540 | A02 | 16047784 | C | T | missense_variant | MODERATE | c.398C>T|p.Thr133Ile |
S9 |
| 195453 | BAA02g28540 | A02 | 16048489 | G | A | missense_variant | MODERATE | c.932G>A|p.Gly311Asp |
S13 S140 S168 S279 S64 |
| 195454 | BAA02g28540 | A02 | 16048582 | C | T | missense_variant | MODERATE | c.1025C>T|p.Ser342Phe |
S9 |
| 195455 | BAA02g28540 | A02 | 16048759 | G | A | missense_variant | MODERATE | c.1202G>A|p.Gly401Glu |
S5 |
| 195456 | BAA02g28540 | A02 | 16049181 | G | A | missense_variant | MODERATE | c.1624G>A|p.Gly542Ser |
S80 |
| 195457 | BAA02g28540 | A02 | 16049219 | G | A | synonymous_variant | LOW | c.1662G>A|p.Ala554Ala |
S33 |
| 195458 | BAA02g28560 | A02 | 16050406 | C | T | upstream_gene_variant | MODIFIER | c.-4397C>T| |
S244 |
| 195459 | BAA02g28550 | A02 | 16051356 | G | A | upstream_gene_variant | MODIFIER | c.-470C>T| |
S134 |
| 195460 | BAA02g28550 | A02 | 16052552 | C | T | upstream_gene_variant | MODIFIER | c.-1666G>A| |
S107 |
| 195461 | BAA02g28550 | A02 | 16052659 | C | T | upstream_gene_variant | MODIFIER | c.-1773G>A| |
S231 |
| 195462 | BAA02g28550 | A02 | 16052914 | G | A | upstream_gene_variant | MODIFIER | c.-2028C>T| |
S38 |
| 195463 | BAA02g28550 | A02 | 16053779 | G | A | upstream_gene_variant | MODIFIER | c.-2893C>T| |
S136 |
| 195464 | BAA02g28560 | A02 | 16055395 | C | T | missense_variant | MODERATE | c.308C>T|p.Ala103Val |
S181 |
| 195465 | BAA02g28550 | A02 | 16055623 | C | T | upstream_gene_variant | MODIFIER | c.-4737G>A| |
S296 |
| 195466 | BAA02g28570 | A02 | 16056159 | C | T | downstream_gene_variant | MODIFIER | c.*4089G>A| |
S185 |
| 195467 | BAA02g28570 | A02 | 16056680 | C | T | downstream_gene_variant | MODIFIER | c.*3568G>A| |
S207 |
| 195468 | BAA02g28560 | A02 | 16056730 | G | A | missense_variant | MODERATE | c.1039G>A|p.Glu347Lys |
S271 |
| 195469 | BAA02g28560 | A02 | 16056733 | C | T | missense_variant | MODERATE | c.1042C>T|p.Leu348Phe |
S268 |
| 195470 | BAA02g28570 | A02 | 16056848 | G | A | downstream_gene_variant | MODIFIER | c.*3400C>T| |
S48 |
| 195471 | BAA02g28570 | A02 | 16057886 | G | A | downstream_gene_variant | MODIFIER | c.*2362C>T| |
S306 S308 |
| 195472 | BAA02g28570 | A02 | 16058012 | G | A | downstream_gene_variant | MODIFIER | c.*2236C>T| |
S45 |
| 195473 | BAA02g28560 | A02 | 16059341 | G | A | downstream_gene_variant | MODIFIER | c.*706G>A| |
S37 |
| 195474 | BAA02g28560 | A02 | 16059369 | G | A | downstream_gene_variant | MODIFIER | c.*734G>A| |
S159 S243 |
| 195475 | BAA02g28560 | A02 | 16059722 | G | A | downstream_gene_variant | MODIFIER | c.*1087G>A| |
S136 |