| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157001 | BAA02g04840 | A02 | 2102736 | C | T | upstream_gene_variant | MODIFIER | c.-1708C>T| |
S292 |
| 157002 | BAA02g04840 | A02 | 2102761 | C | T | upstream_gene_variant | MODIFIER | c.-1683C>T| |
S152 |
| 157003 | BAA02g04840 | A02 | 2103617 | G | A | upstream_gene_variant | MODIFIER | c.-827G>A| |
S177 |
| 157004 | BAA02g04840 | A02 | 2105163 | G | A | synonymous_variant | LOW | c.720G>A|p.Lys240Lys |
S67 |
| 157005 | BAA02g04840 | A02 | 2105318 | C | T | missense_variant | MODERATE | c.875C>T|p.Ala292Val |
S15 S3 |
| 157006 | BAA02g04840 | A02 | 2105576 | G | A | missense_variant | MODERATE | c.1133G>A|p.Gly378Asp |
S177 |
| 157007 | BAA02g04840 | A02 | 2105597 | C | T | missense_variant | MODERATE | c.1154C>T|p.Pro385Leu |
S46 |
| 157008 | BAA02g04840 | A02 | 2105630 | C | T | missense_variant | MODERATE | c.1187C>T|p.Pro396Leu |
S270 |
| 157009 | BAA02g04840 | A02 | 2106249 | G | A | synonymous_variant | LOW | c.1806G>A|p.Leu602Leu |
S291 |
| 157010 | BAA02g04840 | A02 | 2106452 | C | T | downstream_gene_variant | MODIFIER | c.*125C>T| |
S54 |
| 157011 | BAA02g04840 | A02 | 2106690 | G | A | downstream_gene_variant | MODIFIER | c.*363G>A| |
S202 |
| 157012 | BAA02g04840 | A02 | 2106815 | G | A | downstream_gene_variant | MODIFIER | c.*488G>A| |
S166 |
| 157013 | BAA02g04840 | A02 | 2108203 | T | G | downstream_gene_variant | MODIFIER | c.*1876T>G| |
S124 |
| 157014 | BAA02g04840 | A02 | 2108616 | G | A | downstream_gene_variant | MODIFIER | c.*2289G>A| |
S59 |
| 157015 | BAA02g04850 | A02 | 2110986 | G | A | stop_gained | HIGH | c.154C>T|p.Gln52* |
S128 |
| 157016 | BAA02g04850 | A02 | 2111247 | G | A | upstream_gene_variant | MODIFIER | c.-108C>T| |
S246 |
| 157017 | BAA02g04850 | A02 | 2111273 | A | G | upstream_gene_variant | MODIFIER | c.-134T>C| |
S221 |
| 157018 | BAA02g04850 | A02 | 2111530 | C | T | upstream_gene_variant | MODIFIER | c.-391G>A| |
S18 |
| 157019 | BAA02g04850 | A02 | 2111767 | G | A | upstream_gene_variant | MODIFIER | c.-628C>T| |
S52 |
| 157020 | BAA02g04850 | A02 | 2111963 | G | A | upstream_gene_variant | MODIFIER | c.-824C>T| |
S293 |
| 157021 | BAA02g04850 | A02 | 2112316 | A | G | upstream_gene_variant | MODIFIER | c.-1177T>C| |
S81 S85 |
| 157022 | BAA02g04850 | A02 | 2112630 | G | A | upstream_gene_variant | MODIFIER | c.-1491C>T| |
S67 |
| 157023 | BAA02g04850 | A02 | 2112790 | C | T | upstream_gene_variant | MODIFIER | c.-1651G>A| |
S99 |
| 157024 | BAA02g04850 | A02 | 2113006 | G | A | upstream_gene_variant | MODIFIER | c.-1867C>T| |
S82 S92 |
| 157025 | BAA02g04850 | A02 | 2113751 | C | T | upstream_gene_variant | MODIFIER | c.-2612G>A| |
S278 |