| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 77701 | BAA01g41030 | A01 | 27207458 | G | A | upstream_gene_variant | MODIFIER | c.-207G>A| |
S56 |
| 77702 | BAA01g41030 | A01 | 27207512 | C | T | upstream_gene_variant | MODIFIER | c.-153C>T| |
S20 |
| 77703 | BAA01g41030 | A01 | 27207771 | C | T | missense_variant | MODERATE | c.107C>T|p.Pro36Leu |
S44 |
| 77704 | BAA01g41040 | A01 | 27208523 | G | A | upstream_gene_variant | MODIFIER | c.-1164G>A| |
S156 |
| 77705 | BAA01g41040 | A01 | 27209172 | C | T | upstream_gene_variant | MODIFIER | c.-515C>T| |
S291 |
| 77706 | BAA01g41030 | A01 | 27210323 | C | T | downstream_gene_variant | MODIFIER | c.*2151C>T| |
S95 |
| 77707 | BAA01g41040 | A01 | 27210552 | G | A | missense_variant&splice_region_variant | MODERATE | c.325G>A|p.Gly109Arg |
S159 S243 |
| 77708 | BAA01g41040 | A01 | 27210634 | C | T | missense_variant | MODERATE | c.407C>T|p.Ala136Val |
S33 |
| 77709 | BAA01g41040 | A01 | 27210900 | G | A | missense_variant | MODERATE | c.673G>A|p.Ala225Thr |
S179 |
| 77710 | BAA01g41040 | A01 | 27211521 | C | T | missense_variant | MODERATE | c.1211C>T|p.Thr404Ile |
S140 |
| 77711 | BAA01g41040 | A01 | 27211577 | G | A | missense_variant | MODERATE | c.1267G>A|p.Asp423Asn |
S64 |
| 77712 | BAA01g41030 | A01 | 27211792 | C | T | downstream_gene_variant | MODIFIER | c.*3620C>T| |
S187 |
| 77713 | BAA01g41030 | A01 | 27213113 | G | A | downstream_gene_variant | MODIFIER | c.*4941G>A| |
S203 |
| 77714 | BAA01g41050 | A01 | 27213594 | C | T | missense_variant | MODERATE | c.256G>A|p.Glu86Lys |
S280 |
| 77715 | BAA01g41050 | A01 | 27214329 | C | T | upstream_gene_variant | MODIFIER | c.-480G>A| |
S291 |
| 77716 | BAA01g41050 | A01 | 27214497 | G | A | upstream_gene_variant | MODIFIER | c.-648C>T| |
S167 |
| 77717 | BAA01g41050 | A01 | 27215049 | C | T | upstream_gene_variant | MODIFIER | c.-1200G>A| |
S207 |
| 77718 | BAA01g41050 | A01 | 27215380 | G | A | upstream_gene_variant | MODIFIER | c.-1531C>T| |
S198 |
| 77719 | BAA01g41050 | A01 | 27215728 | G | A | upstream_gene_variant | MODIFIER | c.-1879C>T| |
S201 |
| 77720 | BAA01g41050 | A01 | 27215907 | C | T | upstream_gene_variant | MODIFIER | c.-2058G>A| |
S87 |
| 77721 | BAA01g41050 | A01 | 27216752 | C | T | upstream_gene_variant | MODIFIER | c.-2903G>A| |
S278 |
| 77722 | BAA01g41050 | A01 | 27217544 | C | T | upstream_gene_variant | MODIFIER | c.-3695G>A| |
S117 |
| 77723 | BAA01g41060 | A01 | 27219127 | G | A | upstream_gene_variant | MODIFIER | c.-1967C>T| |
S38 |
| 77724 | BAA01g41070 | A01 | 27219957 | C | T | synonymous_variant | LOW | c.930G>A|p.Arg310Arg |
S135 |
| 77725 | BAA01g41070 | A01 | 27220943 | G | A | missense_variant | MODERATE | c.143C>T|p.Thr48Ile |
S23 |