| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 86151 | BAA01g45750 | A01 | 30515872 | C | T | missense_variant | MODERATE | c.58C>T|p.Pro20Ser |
S88 |
| 86152 | BAA01g45750 | A01 | 30516166 | G | A | missense_variant | MODERATE | c.352G>A|p.Gly118Arg |
S2 |
| 86153 | BAA01g45750 | A01 | 30516684 | G | A | synonymous_variant | LOW | c.870G>A|p.Glu290Glu |
S194 |
| 86154 | BAA01g45740 | A01 | 30517392 | C | T | downstream_gene_variant | MODIFIER | c.*3276C>T| |
S266 |
| 86155 | BAA01g45740 | A01 | 30517681 | C | T | downstream_gene_variant | MODIFIER | c.*3565C>T| |
S146 |
| 86156 | BAA01g45760 | A01 | 30518111 | C | T | missense_variant | MODERATE | c.1321G>A|p.Glu441Lys |
S200 S261 S274 S303 |
| 86157 | BAA01g45760 | A01 | 30518653 | G | A | splice_region_variant&intron_variant | LOW | c.1071+8C>T| |
S60 |
| 86158 | BAA01g45760 | A01 | 30520189 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.137-1G>A| |
S233 |
| 86159 | BAA01g45760 | A01 | 30520270 | C | T | splice_donor_variant&intron_variant | HIGH | c.136+1G>A| |
S32 |
| 86160 | BAA01g45760 | A01 | 30520432 | G | A | upstream_gene_variant | MODIFIER | c.-26C>T| |
S87 |
| 86161 | BAA01g45760 | A01 | 30520597 | G | A | upstream_gene_variant | MODIFIER | c.-191C>T| |
S202 |
| 86162 | BAA01g45760 | A01 | 30520732 | C | T | upstream_gene_variant | MODIFIER | c.-326G>A| |
S4 |
| 86163 | BAA01g45760 | A01 | 30523065 | C | T | upstream_gene_variant | MODIFIER | c.-2659G>A| |
S64 |
| 86164 | BAA01g45760 | A01 | 30523264 | G | A | upstream_gene_variant | MODIFIER | c.-2858C>T| |
S262 |
| 86165 | BAA01g45760 | A01 | 30524165 | C | T | upstream_gene_variant | MODIFIER | c.-3759G>A| |
S219 |
| 86166 | BAA01g45770 | A01 | 30525975 | C | T | upstream_gene_variant | MODIFIER | c.-2467G>A| |
S267 |
| 86167 | BAA01g45770 | A01 | 30527629 | G | A | upstream_gene_variant | MODIFIER | c.-4121C>T| |
S292 |
| 86168 | BAA01g45780 | A01 | 30528252 | C | T | missense_variant | MODERATE | c.32C>T|p.Ser11Leu |
S67 |
| 86169 | BAA01g45780 | A01 | 30528285 | C | T | missense_variant | MODERATE | c.65C>T|p.Pro22Leu |
S260 |
| 86170 | BAA01g45780 | A01 | 30528411 | C | T | missense_variant | MODERATE | c.191C>T|p.Ala64Val |
S182 |
| 86171 | BAA01g45780 | A01 | 30528962 | G | A | synonymous_variant | LOW | c.507G>A|p.Arg169Arg |
S5 |
| 86172 | BAA01g45790 | A01 | 30529046 | G | A | upstream_gene_variant | MODIFIER | c.-3816G>A| |
S241 |
| 86173 | BAA01g45790 | A01 | 30529064 | C | T | upstream_gene_variant | MODIFIER | c.-3798C>T| |
S260 |
| 86174 | BAA01g45780 | A01 | 30529236 | G | T | splice_acceptor_variant&intron_variant | HIGH | c.603-1G>T| |
S292 |
| 86175 | BAA01g45780 | A01 | 30529819 | C | T | missense_variant | MODERATE | c.886C>T|p.Leu296Phe |
S127 |