| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 11751 | BAA01g09390 | A01 | 4180727 | G | A | downstream_gene_variant | MODIFIER | c.*2839C>T| |
S308 |
| 11752 | BAA01g09380 | A01 | 4181107 | C | T | splice_region_variant&intron_variant | LOW | c.1183-8C>T| |
S203 |
| 11753 | BAA01g09380 | A01 | 4181810 | G | A | missense_variant | MODERATE | c.1705G>A|p.Val569Ile |
S32 |
| 11754 | BAA01g09380 | A01 | 4181817 | G | A | missense_variant | MODERATE | c.1712G>A|p.Ser571Asn |
S271 |
| 11755 | BAA01g09390 | A01 | 4182373 | G | A | downstream_gene_variant | MODIFIER | c.*1193C>T| |
S17 |
| 11756 | BAA01g09390 | A01 | 4182773 | G | A | downstream_gene_variant | MODIFIER | c.*793C>T| |
S294 |
| 11757 | BAA01g09380 | A01 | 4183315 | G | A | downstream_gene_variant | MODIFIER | c.*334G>A| |
S34 |
| 11758 | BAA01g09380 | A01 | 4183402 | G | A | downstream_gene_variant | MODIFIER | c.*421G>A| |
S297 |
| 11759 | BAA01g09390 | A01 | 4185164 | G | A | missense_variant | MODERATE | c.583C>T|p.Pro195Ser |
S13 |
| 11760 | BAA01g09390 | A01 | 4185214 | G | A | missense_variant | MODERATE | c.533C>T|p.Ala178Val |
S283 |
| 11761 | BAA01g09380 | A01 | 4185417 | G | A | downstream_gene_variant | MODIFIER | c.*2436G>A| |
S37 |
| 11762 | BAA01g09390 | A01 | 4186336 | C | T | upstream_gene_variant | MODIFIER | c.-84G>A| |
S232 |
| 11763 | BAA01g09390 | A01 | 4186456 | G | A | upstream_gene_variant | MODIFIER | c.-204C>T| |
S23 |
| 11764 | BAA01g09400 | A01 | 4187177 | G | A | synonymous_variant | LOW | c.912C>T|p.Tyr304Tyr |
S292 |
| 11765 | BAA01g09400 | A01 | 4187941 | C | T | missense_variant | MODERATE | c.266G>A|p.Gly89Glu |
S70 |
| 11766 | BAA01g09390 | A01 | 4188205 | C | T | upstream_gene_variant | MODIFIER | c.-1953G>A| |
S120 |
| 11767 | BAA01g09400 | A01 | 4188556 | C | T | missense_variant | MODERATE | c.92G>A|p.Gly31Glu |
S286 |
| 11768 | BAA01g09410 | A01 | 4190479 | C | T | missense_variant | MODERATE | c.476G>A|p.Gly159Glu |
S231 |
| 11769 | BAA01g09410 | A01 | 4190663 | C | T | missense_variant | MODERATE | c.292G>A|p.Asp98Asn |
S148 S30 S31 |
| 11770 | BAA01g09400 | A01 | 4191610 | G | A | upstream_gene_variant | MODIFIER | c.-2963C>T| |
S67 |
| 11771 | BAA01g09420 | A01 | 4191821 | G | A | missense_variant | MODERATE | c.538C>T|p.Arg180Trp |
S115 |
| 11772 | BAA01g09400 | A01 | 4193109 | G | A | upstream_gene_variant | MODIFIER | c.-4462C>T| |
S236 |
| 11773 | BAA01g09400 | A01 | 4193568 | G | A | upstream_gene_variant | MODIFIER | c.-4921C>T| |
S115 |
| 11774 | BAA01g09430 | A01 | 4194263 | G | A | missense_variant | MODERATE | c.3955C>T|p.Pro1319Ser |
S37 |
| 11775 | BAA01g09430 | A01 | 4194503 | G | A | missense_variant | MODERATE | c.3803C>T|p.Ser1268Phe |
S190 |