| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 155801 | BAA02g03860 | A02 | 1701635 | C | T | upstream_gene_variant | MODIFIER | c.-2832G>A| |
S186 |
| 155802 | BAA02g03860 | A02 | 1701754 | G | A | upstream_gene_variant | MODIFIER | c.-2951C>T| |
S148 S210 S30 S31 |
| 155803 | BAA02g03880 | A02 | 1702556 | C | T | missense_variant | MODERATE | c.995G>A|p.Gly332Glu |
S306 S308 |
| 155804 | BAA02g03880 | A02 | 1703387 | G | A | missense_variant | MODERATE | c.256C>T|p.Pro86Ser |
S129 |
| 155805 | BAA02g03890 | A02 | 1709126 | G | A | missense_variant&splice_region_variant | MODERATE | c.505G>A|p.Glu169Lys |
S205 |
| 155806 | BAA02g03900 | A02 | 1709583 | G | A | upstream_gene_variant | MODIFIER | c.-375G>A| |
S221 |
| 155807 | BAA02g03900 | A02 | 1710445 | G | A | missense_variant | MODERATE | c.488G>A|p.Arg163Lys |
S98 |
| 155808 | BAA02g03900 | A02 | 1710566 | G | A | synonymous_variant | LOW | c.609G>A|p.Arg203Arg |
S136 |
| 155809 | BAA02g03900 | A02 | 1711189 | C | T | synonymous_variant | LOW | c.1041C>T|p.Cys347Cys |
S23 |
| 155810 | BAA02g03930 | A02 | 1713046 | G | A | upstream_gene_variant | MODIFIER | c.-2557G>A| |
S266 |
| 155811 | BAA02g03920 | A02 | 1713737 | G | A | synonymous_variant | LOW | c.1140C>T|p.Phe380Phe |
S295 |
| 155812 | BAA02g03920 | A02 | 1713741 | G | A | missense_variant | MODERATE | c.1136C>T|p.Ser379Phe |
S35 |
| 155813 | BAA02g03920 | A02 | 1713956 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.922-1G>A| |
S289 S290 |
| 155814 | BAA02g03920 | A02 | 1714377 | C | T | missense_variant | MODERATE | c.694G>A|p.Gly232Arg |
S130 |
| 155815 | BAA02g03920 | A02 | 1714398 | G | A | missense_variant | MODERATE | c.673C>T|p.Pro225Ser |
S279 |
| 155816 | BAA02g03920 | A02 | 1714512 | C | T | missense_variant | MODERATE | c.638G>A|p.Gly213Glu |
S221 |
| 155817 | BAA02g03920 | A02 | 1714924 | C | T | missense_variant | MODERATE | c.226G>A|p.Asp76Asn |
S193 |
| 155818 | BAA02g03930 | A02 | 1715907 | C | T | missense_variant | MODERATE | c.223C>T|p.Pro75Ser |
S186 |
| 155819 | BAA02g03930 | A02 | 1716137 | G | A | synonymous_variant | LOW | c.453G>A|p.Gln151Gln |
S45 |
| 155820 | BAA02g03940 | A02 | 1717120 | C | T | missense_variant | MODERATE | c.1479G>A|p.Met493Ile |
S255 |
| 155821 | BAA02g03940 | A02 | 1717330 | G | A | synonymous_variant | LOW | c.1269C>T|p.Ile423Ile |
S161 |
| 155822 | BAA02g03940 | A02 | 1717626 | G | A | missense_variant | MODERATE | c.973C>T|p.Leu325Phe |
S45 |
| 155823 | BAA02g03940 | A02 | 1718158 | C | T | missense_variant | MODERATE | c.587G>A|p.Gly196Glu |
S111 |
| 155824 | BAA02g03920 | A02 | 1719092 | G | A | upstream_gene_variant | MODIFIER | c.-3943C>T| |
S171 |
| 155825 | BAA02g03920 | A02 | 1719583 | G | A | upstream_gene_variant | MODIFIER | c.-4434C>T| |
S143 |