| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 16901 | BAA01g12750 | A01 | 6034103 | C | T | downstream_gene_variant | MODIFIER | c.*4299C>T| |
S111 |
| 16902 | BAA01g12750 | A01 | 6034207 | G | A | downstream_gene_variant | MODIFIER | c.*4403G>A| |
S37 |
| 16903 | BAA01g12750 | A01 | 6034283 | C | T | downstream_gene_variant | MODIFIER | c.*4479C>T| |
S54 |
| 16904 | BAA01g12750 | A01 | 6034302 | C | T | downstream_gene_variant | MODIFIER | c.*4498C>T| |
S286 |
| 16905 | BAA01g12750 | A01 | 6034732 | C | T | downstream_gene_variant | MODIFIER | c.*4928C>T| |
S264 |
| 16906 | BAA01g12760 | A01 | 6034815 | C | T | intron_variant | MODIFIER | c.2235+2861G>A| |
S151 S263 |
| 16907 | BAA01g12760 | A01 | 6035106 | G | A | intron_variant | MODIFIER | c.2235+2570C>T| |
S116 |
| 16908 | BAA01g12760 | A01 | 6035261 | C | T | intron_variant | MODIFIER | c.2235+2415G>A| |
S296 |
| 16909 | BAA01g12760 | A01 | 6035393 | C | T | intron_variant | MODIFIER | c.2235+2283G>A| |
S261 |
| 16910 | BAA01g12760 | A01 | 6035517 | C | T | intron_variant | MODIFIER | c.2235+2159G>A| |
S79 S84 |
| 16911 | BAA01g12760 | A01 | 6035887 | C | T | intron_variant | MODIFIER | c.2235+1789G>A| |
S169 |
| 16912 | BAA01g12760 | A01 | 6035891 | G | A | intron_variant | MODIFIER | c.2235+1785C>T| |
S281 |
| 16913 | BAA01g12760 | A01 | 6036153 | C | T | intron_variant | MODIFIER | c.2235+1523G>A| |
S135 |
| 16914 | BAA01g12760 | A01 | 6036277 | G | A | intron_variant | MODIFIER | c.2235+1399C>T| |
S234 |
| 16915 | BAA01g12770 | A01 | 6036572 | T | A | downstream_gene_variant | MODIFIER | c.*4833A>T| |
S209 |
| 16916 | BAA01g12770 | A01 | 6036655 | G | A | downstream_gene_variant | MODIFIER | c.*4750C>T| |
S32 |
| 16917 | BAA01g12770 | A01 | 6037166 | G | A | downstream_gene_variant | MODIFIER | c.*4239C>T| |
S180 |
| 16918 | BAA01g12770 | A01 | 6037294 | G | A | downstream_gene_variant | MODIFIER | c.*4111C>T| |
S202 |
| 16919 | BAA01g12770 | A01 | 6037652 | C | T | downstream_gene_variant | MODIFIER | c.*3753G>A| |
S7 |
| 16920 | BAA01g12760 | A01 | 6038324 | G | A | missense_variant | MODERATE | c.1769C>T|p.Ser590Leu |
S183 S198 |
| 16921 | BAA01g12760 | A01 | 6038700 | C | T | missense_variant | MODERATE | c.1393G>A|p.Glu465Lys |
S192 |
| 16922 | BAA01g12760 | A01 | 6038957 | C | T | missense_variant | MODERATE | c.1136G>A|p.Arg379Lys |
S112 S115 |
| 16923 | BAA01g12760 | A01 | 6040672 | G | A | upstream_gene_variant | MODIFIER | c.-280C>T| |
S17 |
| 16924 | BAA01g12770 | A01 | 6042444 | C | T | synonymous_variant | LOW | c.1296G>A|p.Lys432Lys |
S18 |
| 16925 | BAA01g12770 | A01 | 6042602 | C | T | missense_variant | MODERATE | c.1138G>A|p.Ala380Thr |
S50 |