| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 155651 | BAA02g03740 | A02 | 1648823 | C | T | stop_gained | HIGH | c.160C>T|p.Gln54* |
S182 |
| 155652 | BAA02g03750 | A02 | 1649973 | G | A | downstream_gene_variant | MODIFIER | c.*2616C>T| |
S35 |
| 155653 | BAA02g03750 | A02 | 1650170 | G | A | downstream_gene_variant | MODIFIER | c.*2419C>T| |
S197 |
| 155654 | BAA02g03750 | A02 | 1650390 | C | T | downstream_gene_variant | MODIFIER | c.*2199G>A| |
S243 S299 |
| 155655 | BAA02g03750 | A02 | 1650493 | C | T | downstream_gene_variant | MODIFIER | c.*2096G>A| |
S250 |
| 155656 | BAA02g03750 | A02 | 1650661 | G | A | downstream_gene_variant | MODIFIER | c.*1928C>T| |
S50 |
| 155657 | BAA02g03740 | A02 | 1652756 | G | A | downstream_gene_variant | MODIFIER | c.*558G>A| |
S68 |
| 155658 | BAA02g03750 | A02 | 1655159 | C | T | upstream_gene_variant | MODIFIER | c.-663G>A| |
S284 |
| 155659 | BAA02g03760 | A02 | 1656671 | G | A | missense_variant | MODERATE | c.1898C>T|p.Ser633Phe |
S244 |
| 155660 | BAA02g03760 | A02 | 1656905 | C | T | missense_variant | MODERATE | c.1664G>A|p.Arg555Lys |
S289 S290 |
| 155661 | BAA02g03760 | A02 | 1657204 | C | T | stop_gained | HIGH | c.1365G>A|p.Trp455* |
S37 |
| 155662 | BAA02g03760 | A02 | 1660335 | C | T | upstream_gene_variant | MODIFIER | c.-1767G>A| |
S194 |
| 155663 | BAA02g03770 | A02 | 1660757 | G | A | missense_variant | MODERATE | c.464G>A|p.Arg155Lys |
S206 S26 |
| 155664 | BAA02g03770 | A02 | 1661881 | G | A | missense_variant | MODERATE | c.1168G>A|p.Ala390Thr |
S110 |
| 155665 | BAA02g03770 | A02 | 1662028 | C | T | missense_variant | MODERATE | c.1237C>T|p.Pro413Ser |
S242 |
| 155666 | BAA02g03780 | A02 | 1664093 | G | A | upstream_gene_variant | MODIFIER | c.-2957G>A| |
S190 |
| 155667 | BAA02g03780 | A02 | 1664895 | G | A | upstream_gene_variant | MODIFIER | c.-2155G>A| |
S140 |
| 155668 | BAA02g03780 | A02 | 1667058 | G | A | stop_gained | HIGH | c.9G>A|p.Trp3* |
S107 |
| 155669 | BAA02g03780 | A02 | 1667180 | C | T | missense_variant | MODERATE | c.131C>T|p.Ser44Phe |
S97 |
| 155670 | BAA02g03780 | A02 | 1667200 | G | A | missense_variant | MODERATE | c.151G>A|p.Val51Ile |
S209 |
| 155671 | BAA02g03790 | A02 | 1667470 | G | A | upstream_gene_variant | MODIFIER | c.-2154G>A| |
S161 |
| 155672 | BAA02g03790 | A02 | 1667517 | G | A | upstream_gene_variant | MODIFIER | c.-2107G>A| |
S57 |
| 155673 | BAA02g03790 | A02 | 1667562 | G | A | upstream_gene_variant | MODIFIER | c.-2062G>A| |
S25 |
| 155674 | BAA02g03790 | A02 | 1667570 | G | A | upstream_gene_variant | MODIFIER | c.-2054G>A| |
S23 |
| 155675 | BAA02g03780 | A02 | 1668080 | C | T | missense_variant | MODERATE | c.452C>T|p.Ser151Phe |
S103 |