| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 197001 | BAA02g29080-BAA02g29090 | A02 | 16589770 | C | T | intergenic_region | MODIFIER | n.16589770C>T| |
S118 |
| 197002 | BAA02g29080-BAA02g29090 | A02 | 16590028 | G | A | intergenic_region | MODIFIER | n.16590028G>A| |
S97 |
| 197003 | BAA02g29090 | A02 | 16590430 | C | T | upstream_gene_variant | MODIFIER | c.-4633C>T| |
S284 |
| 197004 | BAA02g29090 | A02 | 16590757 | C | T | upstream_gene_variant | MODIFIER | c.-4306C>T| |
S203 |
| 197005 | BAA02g29090 | A02 | 16591772 | G | A | upstream_gene_variant | MODIFIER | c.-3291G>A| |
S48 |
| 197006 | BAA02g29090 | A02 | 16592290 | C | T | upstream_gene_variant | MODIFIER | c.-2773C>T| |
S177 |
| 197007 | BAA02g29090 | A02 | 16593218 | T | A | upstream_gene_variant | MODIFIER | c.-1845T>A| |
S130 |
| 197008 | BAA02g29090 | A02 | 16593311 | C | T | upstream_gene_variant | MODIFIER | c.-1752C>T| |
S2 |
| 197009 | BAA02g29090 | A02 | 16593519 | C | T | upstream_gene_variant | MODIFIER | c.-1544C>T| |
S83 S88 |
| 197010 | BAA02g29090 | A02 | 16593625 | G | A | upstream_gene_variant | MODIFIER | c.-1438G>A| |
S246 |
| 197011 | BAA02g29090 | A02 | 16594807 | C | T | upstream_gene_variant | MODIFIER | c.-256C>T| |
S118 |
| 197012 | BAA02g29110 | A02 | 16595750 | C | T | upstream_gene_variant | MODIFIER | c.-3490C>T| |
S77 S82 |
| 197013 | BAA02g29090 | A02 | 16596199 | G | A | missense_variant | MODERATE | c.878G>A|p.Arg293Lys |
S7 |
| 197014 | BAA02g29110 | A02 | 16596402 | C | T | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S182 |
| 197015 | BAA02g29110 | A02 | 16596867 | C | T | upstream_gene_variant | MODIFIER | c.-2373C>T| |
S234 |
| 197016 | BAA02g29110 | A02 | 16597146 | G | A | upstream_gene_variant | MODIFIER | c.-2094G>A| |
S202 |
| 197017 | BAA02g29100 | A02 | 16597443 | C | T | synonymous_variant | LOW | c.582G>A|p.Leu194Leu |
S77 |
| 197018 | BAA02g29100 | A02 | 16597449 | C | T | synonymous_variant | LOW | c.576G>A|p.Val192Val |
S112 |
| 197019 | BAA02g29100 | A02 | 16597742 | C | T | missense_variant | MODERATE | c.283G>A|p.Gly95Arg |
S119 |
| 197020 | BAA02g29100 | A02 | 16597751 | C | T | missense_variant | MODERATE | c.274G>A|p.Val92Ile |
S301 S304 |
| 197021 | BAA02g29100 | A02 | 16597766 | C | T | missense_variant | MODERATE | c.259G>A|p.Glu87Lys |
S140 |
| 197022 | BAA02g29100 | A02 | 16598505 | G | A | upstream_gene_variant | MODIFIER | c.-481C>T| |
S187 |
| 197023 | BAA02g29100 | A02 | 16599218 | C | T | upstream_gene_variant | MODIFIER | c.-1194G>A| |
S233 |
| 197024 | BAA02g29110 | A02 | 16599675 | G | A | missense_variant | MODERATE | c.283G>A|p.Asp95Asn |
S4 |
| 197025 | BAA02g29100 | A02 | 16599717 | C | T | upstream_gene_variant | MODIFIER | c.-1693G>A| |
S112 |