| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 179601 | BAA02g19910 | A02 | 10457325 | C | T | upstream_gene_variant | MODIFIER | c.-992C>T| |
S308 |
| 179602 | BAA02g19910 | A02 | 10458686 | C | T | missense_variant | MODERATE | c.370C>T|p.Arg124Trp |
S271 |
| 179603 | BAA02g19910 | A02 | 10459083 | C | T | missense_variant | MODERATE | c.767C>T|p.Pro256Leu |
S120 |
| 179604 | BAA02g19920 | A02 | 10459777 | C | A | upstream_gene_variant | MODIFIER | c.-633C>A| |
S209 |
| 179605 | BAA02g19920 | A02 | 10461274 | G | A | splice_region_variant&intron_variant | LOW | c.481+6G>A| |
S263 |
| 179606 | BAA02g19920 | A02 | 10461461 | G | A | missense_variant | MODERATE | c.569G>A|p.Arg190Lys |
S247 |
| 179607 | BAA02g19910 | A02 | 10461721 | G | A | downstream_gene_variant | MODIFIER | c.*2391G>A| |
S202 |
| 179608 | BAA02g19910 | A02 | 10461993 | G | A | downstream_gene_variant | MODIFIER | c.*2663G>A| |
S144 |
| 179609 | BAA02g19910 | A02 | 10462286 | C | T | downstream_gene_variant | MODIFIER | c.*2956C>T| |
S289 S290 |
| 179610 | BAA02g19910 | A02 | 10462650 | G | A | downstream_gene_variant | MODIFIER | c.*3320G>A| |
S232 |
| 179611 | BAA02g19910 | A02 | 10462904 | C | T | downstream_gene_variant | MODIFIER | c.*3574C>T| |
S261 |
| 179612 | BAA02g19910 | A02 | 10463324 | G | A | downstream_gene_variant | MODIFIER | c.*3994G>A| |
S146 |
| 179613 | BAA02g19930 | A02 | 10464258 | G | A | upstream_gene_variant | MODIFIER | c.-743C>T| |
S148 S30 S31 |
| 179614 | BAA02g19930 | A02 | 10466922 | G | A | upstream_gene_variant | MODIFIER | c.-3407C>T| |
S109 |
| 179615 | BAA02g19930 | A02 | 10467134 | C | T | upstream_gene_variant | MODIFIER | c.-3619G>A| |
S140 |
| 179616 | BAA02g19940 | A02 | 10468877 | A | C | missense_variant | MODERATE | c.296A>C|p.Asn99Thr |
S126 S228 S239 S243 S257 S260 S286 S99 |
| 179617 | BAA02g19940 | A02 | 10469044 | C | T | stop_gained | HIGH | c.463C>T|p.Gln155* |
S114 S242 |
| 179618 | BAA02g19940 | A02 | 10469476 | C | T | synonymous_variant | LOW | c.783C>T|p.Asp261Asp |
S81 |
| 179619 | BAA02g19940 | A02 | 10469477 | G | A | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S113 |
| 179620 | BAA02g19940 | A02 | 10469710 | C | T | stop_gained | HIGH | c.916C>T|p.Gln306* |
S38 |
| 179621 | BAA02g19940 | A02 | 10469856 | G | A | synonymous_variant | LOW | c.1062G>A|p.Ala354Ala |
S51 |
| 179622 | BAA02g19950 | A02 | 10470689 | G | A | upstream_gene_variant | MODIFIER | c.-2499G>A| |
S59 |
| 179623 | BAA02g19950 | A02 | 10470841 | G | A | upstream_gene_variant | MODIFIER | c.-2347G>A| |
S188 |
| 179624 | BAA02g19950 | A02 | 10471750 | C | T | upstream_gene_variant | MODIFIER | c.-1438C>T| |
S13 S140 S168 S279 S64 |
| 179625 | BAA02g19950 | A02 | 10473060 | C | T | upstream_gene_variant | MODIFIER | c.-128C>T| |
S63 |