| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164901 | BAA02g11200 | A02 | 5066901 | G | A | upstream_gene_variant | MODIFIER | c.-3421C>T| |
S50 |
| 164902 | BAA02g11200 | A02 | 5067008 | G | A | upstream_gene_variant | MODIFIER | c.-3528C>T| |
S107 |
| 164903 | BAA02g11220 | A02 | 5067624 | C | T | synonymous_variant | LOW | c.495G>A|p.Glu165Glu |
S51 S85 |
| 164904 | BAA02g11220 | A02 | 5068392 | C | T | missense_variant | MODERATE | c.325G>A|p.Asp109Asn |
S219 |
| 164905 | BAA02g11220 | A02 | 5068556 | G | A | missense_variant | MODERATE | c.161C>T|p.Pro54Leu |
S271 |
| 164906 | BAA02g11210 | A02 | 5069517 | G | A | upstream_gene_variant | MODIFIER | c.-3030C>T| |
S19 |
| 164907 | BAA02g11230 | A02 | 5070061 | G | A | missense_variant | MODERATE | c.377G>A|p.Ser126Asn |
S136 |
| 164908 | BAA02g11230 | A02 | 5070100 | G | A | missense_variant | MODERATE | c.416G>A|p.Ser139Asn |
S132 S137 S215 |
| 164909 | BAA02g11210 | A02 | 5070377 | G | A | upstream_gene_variant | MODIFIER | c.-3890C>T| |
S294 |
| 164910 | BAA02g11240 | A02 | 5072312 | G | A | missense_variant | MODERATE | c.656C>T|p.Pro219Leu |
S221 |
| 164911 | BAA02g11240 | A02 | 5072738 | G | A | missense_variant | MODERATE | c.230C>T|p.Ser77Phe |
S11 S282 |
| 164912 | BAA02g11220 | A02 | 5073298 | C | T | upstream_gene_variant | MODIFIER | c.-4582G>A| |
S178 |
| 164913 | BAA02g11220 | A02 | 5073365 | C | T | upstream_gene_variant | MODIFIER | c.-4649G>A| |
S120 |
| 164914 | BAA02g11240 | A02 | 5074318 | G | A | upstream_gene_variant | MODIFIER | c.-1351C>T| |
S4 |
| 164915 | BAA02g11250 | A02 | 5074652 | G | A | missense_variant | MODERATE | c.208G>A|p.Glu70Lys |
S169 |
| 164916 | BAA02g11250 | A02 | 5075163 | G | A | missense_variant | MODERATE | c.719G>A|p.Gly240Asp |
S247 |
| 164917 | BAA02g11250 | A02 | 5075312 | G | A | missense_variant | MODERATE | c.868G>A|p.Ala290Thr |
S198 |
| 164918 | BAA02g11250 | A02 | 5076161 | C | T | missense_variant | MODERATE | c.1661C>T|p.Pro554Leu |
S117 |
| 164919 | BAA02g11250 | A02 | 5076247 | C | T | missense_variant | MODERATE | c.1747C>T|p.Pro583Ser |
S90 |
| 164920 | BAA02g11250 | A02 | 5076319 | G | A | missense_variant | MODERATE | c.1819G>A|p.Gly607Arg |
S51 |
| 164921 | BAA02g11240 | A02 | 5076662 | G | A | upstream_gene_variant | MODIFIER | c.-3695C>T| |
S165 |
| 164922 | BAA02g11260 | A02 | 5078754 | G | A | missense_variant&splice_region_variant | MODERATE | c.20G>A|p.Arg7Lys |
S81 S85 |
| 164923 | BAA02g11250 | A02 | 5078874 | G | A | downstream_gene_variant | MODIFIER | c.*2436G>A| |
S166 |
| 164924 | BAA02g11260 | A02 | 5079062 | C | T | stop_gained | HIGH | c.31C>T|p.Gln11* |
S200 |
| 164925 | BAA02g11260 | A02 | 5079130 | C | T | synonymous_variant | LOW | c.99C>T|p.Asp33Asp |
S292 |