| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 161651 | BAA02g08710 | A02 | 3855385 | C | T | missense_variant | MODERATE | c.356C>T|p.Ser119Phe |
S127 |
| 161652 | BAA02g08710 | A02 | 3855681 | C | T | synonymous_variant | LOW | c.652C>T|p.Leu218Leu |
S25 |
| 161653 | BAA02g08710 | A02 | 3855688 | G | A | missense_variant | MODERATE | c.659G>A|p.Ser220Asn |
S217 S248 |
| 161654 | BAA02g08710 | A02 | 3855978 | G | A | missense_variant | MODERATE | c.949G>A|p.Ala317Thr |
S13 S140 S168 S279 S64 |
| 161655 | BAA02g08710 | A02 | 3855995 | G | A | synonymous_variant | LOW | c.966G>A|p.Glu322Glu |
S229 |
| 161656 | BAA02g08720 | A02 | 3856415 | G | A | upstream_gene_variant | MODIFIER | c.-1656G>A| |
S11 |
| 161657 | BAA02g08720 | A02 | 3856780 | G | A | upstream_gene_variant | MODIFIER | c.-1291G>A| |
S156 |
| 161658 | BAA02g08720 | A02 | 3857177 | G | A | upstream_gene_variant | MODIFIER | c.-894G>A| |
S271 |
| 161659 | BAA02g08720 | A02 | 3857580 | G | T | upstream_gene_variant | MODIFIER | c.-491G>T| |
|
| 161660 | BAA02g08720 | A02 | 3857852 | C | T | upstream_gene_variant | MODIFIER | c.-219C>T| |
S272 |
| 161661 | BAA02g08720 | A02 | 3858119 | G | A | missense_variant | MODERATE | c.49G>A|p.Ala17Thr |
S295 |
| 161662 | BAA02g08720 | A02 | 3858257 | G | A | missense_variant | MODERATE | c.187G>A|p.Asp63Asn |
S296 |
| 161663 | BAA02g08730 | A02 | 3860951 | G | A | upstream_gene_variant | MODIFIER | c.-926C>T| |
S35 |
| 161664 | BAA02g08730 | A02 | 3862224 | G | A | upstream_gene_variant | MODIFIER | c.-2199C>T| |
S136 |
| 161665 | BAA02g08730 | A02 | 3862502 | C | T | upstream_gene_variant | MODIFIER | c.-2477G>A| |
S211 S227 |
| 161666 | BAA02g08740 | A02 | 3865569 | C | T | missense_variant | MODERATE | c.1355G>A|p.Ser452Asn |
S127 |
| 161667 | BAA02g08740 | A02 | 3865596 | G | A | missense_variant | MODERATE | c.1328C>T|p.Ala443Val |
S197 |
| 161668 | BAA02g08740 | A02 | 3866542 | C | T | missense_variant | MODERATE | c.746G>A|p.Gly249Asp |
S111 |
| 161669 | BAA02g08740 | A02 | 3866589 | C | T | synonymous_variant | LOW | c.699G>A|p.Glu233Glu |
S66 |
| 161670 | BAA02g08740 | A02 | 3866715 | G | A | synonymous_variant | LOW | c.573C>T|p.Asn191Asn |
S80 |
| 161671 | BAA02g08740 | A02 | 3866752 | G | A | missense_variant | MODERATE | c.536C>T|p.Ser179Phe |
S80 |
| 161672 | BAA02g08740 | A02 | 3868818 | C | T | upstream_gene_variant | MODIFIER | c.-1531G>A| |
S270 |
| 161673 | BAA02g08740 | A02 | 3869934 | G | A | upstream_gene_variant | MODIFIER | c.-2647C>T| |
S187 |
| 161674 | BAA02g08760 | A02 | 3870832 | G | A | missense_variant | MODERATE | c.1073C>T|p.Pro358Leu |
S1 |
| 161675 | BAA02g08740 | A02 | 3871916 | G | A | upstream_gene_variant | MODIFIER | c.-4629C>T| |
S37 |